#mapping_provider: RGD
#mapping_tool: RGD SSSOM file generator
#mapping_tool_version: RGD SSSOM File Generator -- build 2024-07-24
#mapping_set_id: https://download.rgd.mcw.edu/ontology/mappings/efo_rdo_rgd.sssom.tsv.txt
#mapping_set_title: All mappings of EFO terms to RDO terms generated by RGD (draft version)
#mapping_set_description: All mappings of EFO terms to RDO terms generated by RGD (draft version)
#license: https://creativecommons.org/licenses/by/4.0/
#object_source: obo:EFO
#subject_source: obo:RDO
#curie_map:
# EFO: http://purl.obolibrary.org/obo/EFO_
# RDO: http://purl.obolibrary.org/obo/RDO_
# skos: http://www.w3.org/2004/02/skos/core#
# orcid: https://orcid.org/
# obo: http://purl.obolibrary.org/obo/
# semapv: https://w3id.org/semapv/vocab/
object_id	object_label	predicate_id	subject_id	subject_label	mapping_justification	mapping_date
EFO:0000094	B-cell acute lymphoblastic leukemia	skos:exactMatch	DOID:0080630	B-lymphoblastic leukemia/lymphoma	semapv:ManualMappingCuration	2022-07-21
EFO:0000094	B-cell acute lymphoblastic leukemia	skos:exactMatch	DOID:0080638	B-cell acute lymphoblastic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:0000095	chronic lymphocytic leukemia	skos:exactMatch	DOID:1040	chronic lymphocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000096	neoplasm of mature B-cells	skos:exactMatch	DOID:706	mature B-cell neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0000174	Ewing sarcoma	skos:exactMatch	DOID:3369	Ewing sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000178	gastric carcinoma	skos:exactMatch	DOID:10538	gastric fundus cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0000178	gastric carcinoma	skos:exactMatch	DOID:5517	stomach carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000180	HIV-1 infection	skos:exactMatch	DOID:526	human immunodeficiency virus infectious disease	semapv:ManualMappingCuration	2023-12-04
EFO:0000181	head and neck squamous cell carcinoma	skos:exactMatch	DOID:5520	head and neck squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000182	hepatocellular carcinoma	skos:exactMatch	DOID:684	hepatocellular carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000182	hepatocellular carcinoma	skos:exactMatch	DOID:686	liver carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000183	Hodgkins lymphoma	skos:exactMatch	DOID:8567	Hodgkin's lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000186	invasive breast ductal carcinoma	skos:exactMatch	DOID:3008	invasive ductal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000191	MALT lymphoma	skos:exactMatch	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue	semapv:ManualMappingCuration	2022-01-24
EFO:0000195	metabolic syndrome	skos:exactMatch	DOID:14221	abdominal obesity-metabolic syndrome 1	semapv:ManualMappingCuration	2022-01-24
EFO:0000195	metabolic syndrome	skos:exactMatch	DOID:9006646	Metabolic Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0000196	metastatic prostate cancer	skos:exactMatch	DOID:10283	prostate cancer	semapv:ManualMappingCuration	2023-12-04
EFO:0000197	mucinous carcinoma	skos:exactMatch	DOID:3030	mucinous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000198	myelodysplastic syndrome	skos:exactMatch	DOID:0050908	myelodysplastic syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0000199	oral squamous cell carcinoma	skos:exactMatch	DOID:0050866	oral squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000200	plasma cell neoplasm	skos:exactMatch	DOID:6536	plasma cell neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0000203	monoclonal gammopathy	skos:exactMatch	DOID:7442	monoclonal gammopathy of uncertain significance	semapv:ManualMappingCuration	2022-01-24
EFO:0000205	stage I endometrioid carcinoma	skos:exactMatch	DOID:9004265	Endometrioid Carcinomas	semapv:ManualMappingCuration	2023-12-04
EFO:0000206	stage II endometrioid carcinoma	skos:exactMatch	DOID:9004265	Endometrioid Carcinomas	semapv:ManualMappingCuration	2023-12-04
EFO:0000209	T-cell acute lymphoblastic leukemia	skos:exactMatch	DOID:5603	T-cell acute lymphoblastic leukemia	semapv:ManualMappingCuration	2023-03-06
EFO:0000211	unspecified peripheral T-cell lymphoma	skos:exactMatch	DOID:0050749	peripheral T-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:0000216	acinar cell carcinoma	skos:exactMatch	DOID:3025	acinar cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000217	gastritis	skos:exactMatch	DOID:4029	gastritis	semapv:ManualMappingCuration	2022-01-24
EFO:0000218	acute erythroleukemia	skos:exactMatch	DOID:0080780	acute erythroid leukemia	semapv:ManualMappingCuration	2023-03-17
EFO:0000218	acute erythroleukemia	skos:exactMatch	DOID:9000647	Acute Erythroleukemia	semapv:ManualMappingCuration	2023-12-04
EFO:0000220	acute lymphoblastic leukemia	skos:exactMatch	DOID:1037	lymphoid leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000220	acute lymphoblastic leukemia	skos:exactMatch	DOID:9952	acute lymphoblastic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000221	acute monocytic leukemia	skos:exactMatch	DOID:8864	acute monocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000222	acute myeloid leukemia	skos:exactMatch	DOID:9119	acute myeloid leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000223	acute myelomonocytic leukemia	skos:exactMatch	DOID:0081082	acute myelomonocytic leukemia	semapv:ManualMappingCuration	2023-04-17
EFO:0000224	acute promyelocytic leukemia	skos:exactMatch	DOID:0060318	acute promyelocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000224	acute promyelocytic leukemia	skos:exactMatch	DOID:0081081	acute promyelocytic leukemia with PML-RARA	semapv:ManualMappingCuration	2023-04-17
EFO:0000225	acute quadriplegic myopathy	skos:exactMatch	DOID:423	myopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0000228	adenocarcinoma	skos:exactMatch	DOID:299	adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000231	adenoid cystic carcinoma	skos:exactMatch	DOID:0080202	adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000232	adenoma	skos:exactMatch	DOID:657	adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000233	adenosquamous lung carcinoma	skos:exactMatch	DOID:4829	adenosquamous lung carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000239	adrenal gland pheochromocytoma	skos:exactMatch	DOID:0050892	adrenal gland pheochromocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000248	alveolar rhabdomyosarcoma	skos:exactMatch	DOID:4051	alveolar rhabdomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000255	angioimmunoblastic T-cell lymphoma	skos:exactMatch	DOID:0111147	angioimmunoblastic T-cell lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000266	aortic stenosis	skos:exactMatch	DOID:1712	aortic valve stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0000272	astrocytoma	skos:exactMatch	DOID:3069	malignant astrocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000274	atopic eczema	skos:exactMatch	DOID:3310	atopic dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0000275	atrial fibrillation	skos:exactMatch	DOID:0060224	atrial fibrillation	semapv:ManualMappingCuration	2022-01-24
EFO:0000278	pancreatitis	skos:exactMatch	DOID:4989	pancreatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0000279	azoospermia	skos:exactMatch	DOID:0111910	spermatogenic failure	semapv:ManualMappingCuration	2022-07-21
EFO:0000279	azoospermia	skos:exactMatch	DOID:14227	azoospermia	semapv:ManualMappingCuration	2022-01-24
EFO:0000280	Barrett's esophagus	skos:exactMatch	DOID:9206	Barrett's esophagus	semapv:ManualMappingCuration	2022-01-24
EFO:0000281	basal-like breast carcinoma	skos:exactMatch	DOID:3458	breast adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0000284	benign prostatic hyperplasia	skos:exactMatch	DOID:11132	prostatic hypertrophy	semapv:ManualMappingCuration	2022-01-24
EFO:0000284	benign prostatic hyperplasia	skos:exactMatch	DOID:2883	prostatic adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000294	bladder tumor	skos:exactMatch	DOID:9009116	Urinary Bladder Neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:0000304	breast adenocarcinoma	skos:exactMatch	DOID:3458	breast adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000305	breast carcinoma	skos:exactMatch	DOID:3459	breast carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000306	breast tumor luminal	skos:exactMatch	DOID:0060548	luminal breast carcinoma A	semapv:ManualMappingCuration	2022-01-24
EFO:0000308	bronchoalveolar adenocarcinoma	skos:exactMatch	DOID:4926	bronchiolo-alveolar adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000309	Burkitts lymphoma	skos:exactMatch	DOID:8584	Burkitt lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000313	carcinoma	skos:exactMatch	DOID:305	carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000318	cardiomyopathy	skos:exactMatch	DOID:0050700	cardiomyopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0000319	cardiovascular disease	skos:exactMatch	DOID:1287	cardiovascular system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000326	central nervous system cancer	skos:exactMatch	DOID:3620	central nervous system cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0000330	childhood acute myeloid leukemia	skos:exactMatch	DOID:0070323	childhood acute myeloid leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000331	chondroblastoma	skos:exactMatch	DOID:2649	chondroblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000332	chondromyxoid fibroma	skos:exactMatch	DOID:9001119	chondromyxoid fibroma	semapv:ManualMappingCuration	2023-12-04
EFO:0000333	chondrosarcoma	skos:exactMatch	DOID:3371	chondrosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000335	chromophobe renal cell carcinoma	skos:exactMatch	DOID:4471	chromophobe renal cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000336	chromosomal aberration	skos:exactMatch	DOID:9004814	Chromosome Aberrations	semapv:ManualMappingCuration	2023-12-04
EFO:0000337	chronic gastritis	skos:exactMatch	DOID:4029	gastritis	semapv:ManualMappingCuration	2022-01-24
EFO:0000339	chronic myelogenous leukemia	skos:exactMatch	DOID:0081088	chronic myelogenous leukemia, BCR-ABL1 positive	semapv:ManualMappingCuration	2023-03-17
EFO:0000339	chronic myelogenous leukemia	skos:exactMatch	DOID:8552	chronic myeloid leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000341	chronic obstructive pulmonary disease	skos:exactMatch	DOID:3083	chronic obstructive pulmonary disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000342	chronic pancreatitis	skos:exactMatch	DOID:9006190	Chronic Pancreatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0000348	clear cell adenocarcinoma	skos:exactMatch	DOID:4468	clear cell adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000349	clear cell renal carcinoma	skos:exactMatch	DOID:4467	clear cell renal cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000350	clear cell sarcoma of the kidney	skos:exactMatch	DOID:4880	kidney clear cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000364	colon mucinous adenocarcinoma	skos:exactMatch	DOID:3029	colon mucinous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000365	colorectal adenocarcinoma	skos:exactMatch	DOID:0050861	colorectal adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000365	colorectal adenocarcinoma	skos:exactMatch	DOID:0050913	large intestine adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000373	congestive heart failure	skos:exactMatch	DOID:6000	congestive heart failure	semapv:ManualMappingCuration	2022-01-24
EFO:0000384	Crohn's disease	skos:exactMatch	DOID:8778	Crohn's disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000389	cutaneous melanoma	skos:exactMatch	DOID:8923	skin melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000394	dedifferentiated chondrosarcoma	skos:exactMatch	DOID:0081247	dedifferentiated chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
EFO:0000397	dermal neurofibroma	skos:exactMatch	DOID:962	neurofibroma	semapv:ManualMappingCuration	2023-12-04
EFO:0000398	dermatomyositis	skos:exactMatch	DOID:10223	dermatomyositis	semapv:ManualMappingCuration	2022-01-24
EFO:0000400	diabetes mellitus	skos:exactMatch	DOID:9351	diabetes mellitus	semapv:ManualMappingCuration	2022-01-24
EFO:0000401	diabetic nephropathy	skos:exactMatch	DOID:9002165	Diabetic Nephropathies	semapv:ManualMappingCuration	2023-12-04
EFO:0000402	diffuse gastric adenocarcinoma	skos:exactMatch	DOID:6217	gastric diffuse adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000403	diffuse large B-cell lymphoma	skos:exactMatch	DOID:0050745	diffuse large B-cell lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000404	diffuse scleroderma	skos:exactMatch	DOID:1580	diffuse scleroderma	semapv:ManualMappingCuration	2022-01-24
EFO:0000405	digestive system disease	skos:exactMatch	DOID:5295	intestinal disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000405	digestive system disease	skos:exactMatch	DOID:77	gastrointestinal system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000407	dilated cardiomyopathy	skos:exactMatch	DOID:12930	dilated cardiomyopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0000408	disease	skos:exactMatch	DOID:4	disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000432	breast ductal carcinoma in situ	skos:exactMatch	DOID:0060074	ductal carcinoma in situ	semapv:ManualMappingCuration	2022-01-24
EFO:0000437	embryonal rhabdomyosarcoma	skos:exactMatch	DOID:3246	embryonal rhabdomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000464	emphysema	skos:exactMatch	DOID:9675	pulmonary emphysema	semapv:ManualMappingCuration	2022-01-24
EFO:0000465	endocarditis	skos:exactMatch	DOID:10314	endocarditis	semapv:ManualMappingCuration	2022-01-24
EFO:0000466	endometrioid carcinoma	skos:exactMatch	DOID:9004265	Endometrioid Carcinomas	semapv:ManualMappingCuration	2023-12-04
EFO:0000474	epilepsy	skos:exactMatch	DOID:1826	epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:0000478	esophageal adenocarcinoma	skos:exactMatch	DOID:4914	esophagus adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000479	essential thrombocythemia	skos:exactMatch	DOID:2224	essential thrombocythemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000489	extra-adrenal sympathetic paraganglioma	skos:exactMatch	DOID:0050773	paraganglioma	semapv:ManualMappingCuration	2023-12-04
EFO:0000489	extra-adrenal sympathetic paraganglioma	skos:exactMatch	DOID:0050936	extra-adrenal pheochromocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000495	fetal growth restriction	skos:exactMatch	DOID:9002231	Fetal Growth Retardation	semapv:ManualMappingCuration	2023-12-04
EFO:0000497	fibromatosis	skos:exactMatch	DOID:0050871	fibroma	semapv:ManualMappingCuration	2023-12-04
EFO:0000499	follicular thyroid adenoma	skos:exactMatch	DOID:2891	thyroid adenoma	semapv:ManualMappingCuration	2023-03-06
EFO:0000499	follicular thyroid adenoma	skos:exactMatch	DOID:6204	follicular adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000500	ganglioneuroma	skos:exactMatch	DOID:4817	ganglioneuroma	semapv:ManualMappingCuration	2022-01-24
EFO:0000501	follicular thyroid carcinoma	skos:exactMatch	DOID:3962	follicular thyroid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000502	ganglioneuroblastoma	skos:exactMatch	DOID:4163	ganglioneuroblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000503	gastric adenocarcinoma	skos:exactMatch	DOID:3717	gastric adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000504	gastric intestinal type adenocarcinoma	skos:exactMatch	DOID:3717	gastric adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0000508	genetic disorder	skos:exactMatch	DOID:630	genetic disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000512	reproductive system disease	skos:exactMatch	DOID:15	reproductive system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000514	germ cell tumor	skos:exactMatch	DOID:2994	germ cell cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0000514	germ cell tumor	skos:exactMatch	DOID:9005127	germ cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:0000514	germ cell tumor	skos:exactMatch	DOID:9005959	Gonadal Tissue Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0000519	glioblastoma multiforme	skos:exactMatch	DOID:3068	glioblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000524	head and neck disorder	skos:exactMatch	DOID:7	disease of anatomical entity	semapv:ManualMappingCuration	2023-12-04
EFO:0000536	hyperplasia	skos:exactMatch	DOID:9002221	Hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0000537	hypertension	skos:exactMatch	DOID:10763	hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:0000538	hypertrophic cardiomyopathy	skos:exactMatch	DOID:11984	hypertrophic cardiomyopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0000540	immune system disease	skos:exactMatch	DOID:2914	immune system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000544	infection	skos:exactMatch	DOID:0050117	disease by infectious agent	semapv:ManualMappingCuration	2023-12-04
EFO:0000545	infertility	skos:exactMatch	DOID:5223	infertility	semapv:ManualMappingCuration	2022-01-24
EFO:0000546	injury	skos:exactMatch	DOID:9001600	Wounds and Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0000549	insulinoma	skos:exactMatch	DOID:3892	insulinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0000551	intracranial hemorrhage	skos:exactMatch	DOID:9003104	Intracranial Hemorrhages	semapv:ManualMappingCuration	2023-12-04
EFO:0000552	invasive breast ductal and lobular carcinoma	skos:exactMatch	DOID:3008	invasive ductal carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0000553	invasive lobular carcinoma	skos:exactMatch	DOID:3457	invasive lobular carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000555	irritable bowel syndrome	skos:exactMatch	DOID:9778	irritable bowel syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0000556	ischemia	skos:exactMatch	DOID:326	ischemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000557	juvenile dermatomyositis	skos:exactMatch	DOID:14203	childhood type dermatomyositis	semapv:ManualMappingCuration	2022-01-24
EFO:0000558	Kaposi's sarcoma	skos:exactMatch	DOID:8632	Kaposi's sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000559	keratinizing squamous cell carcinoma	skos:exactMatch	DOID:5521	keratinizing squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000563	large cell neuroendocrine carcinoma	skos:exactMatch	DOID:0050872	large cell neuroendocrine carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000564	leiomyosarcoma	skos:exactMatch	DOID:1967	leiomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000565	leukemia	skos:exactMatch	DOID:1240	leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0000569	liposarcoma	skos:exactMatch	DOID:3382	liposarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000571	lung adenocarcinoma	skos:exactMatch	DOID:3910	lung adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000574	lymphoma	skos:exactMatch	DOID:0060058	lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000580	medullary breast carcinoma	skos:exactMatch	DOID:5605	breast medullary carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000584	infectious meningitis	skos:exactMatch	DOID:9471	meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:0000588	mesothelioma	skos:exactMatch	DOID:9003566	Mesothelioma	semapv:ManualMappingCuration	2023-12-04
EFO:0000589	metabolic disease	skos:exactMatch	DOID:0014667	disease of metabolism	semapv:ManualMappingCuration	2022-01-24
EFO:0000595	monophasic synovial sarcoma	skos:exactMatch	DOID:5495	monophasic synovial sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000612	myocardial infarction	skos:exactMatch	DOID:5844	myocardial infarction	semapv:ManualMappingCuration	2022-01-24
EFO:0000613	myxoid liposarcoma	skos:exactMatch	DOID:5363	myxoid liposarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000613	myxoid liposarcoma	skos:exactMatch	DOID:5709	mixed-type liposarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000616	neoplasm	skos:exactMatch	DOID:14566	disease of cellular proliferation	semapv:ManualMappingCuration	2022-01-24
EFO:0000618	nervous system disease	skos:exactMatch	DOID:863	nervous system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000621	neuroblastoma	skos:exactMatch	DOID:769	neuroblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000622	neurofibroma	skos:exactMatch	DOID:962	neurofibroma	semapv:ManualMappingCuration	2022-01-24
EFO:0000625	nevus	skos:exactMatch	DOID:9002969	Nevus	semapv:ManualMappingCuration	2023-12-04
EFO:0000630	oligoastrocytoma	skos:exactMatch	DOID:7912	mixed oligodendroglioma-astrocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000632	oligodendroglioma	skos:exactMatch	DOID:3181	oligodendroglioma	semapv:ManualMappingCuration	2022-01-24
EFO:0000637	osteosarcoma	skos:exactMatch	DOID:3347	osteosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000639	papillary cystadenocarcinoma	skos:exactMatch	DOID:3110	papillary cystadenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000640	papillary renal cell carcinoma	skos:exactMatch	DOID:4465	papillary renal cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000641	papillary thyroid carcinoma	skos:exactMatch	DOID:3969	papillary thyroid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000649	periodontitis	skos:exactMatch	DOID:824	periodontitis	semapv:ManualMappingCuration	2022-01-24
EFO:0000649	periodontitis	skos:exactMatch	DOID:9893	periodontosis	semapv:ManualMappingCuration	2022-01-24
EFO:0000650	whooping cough	skos:exactMatch	DOID:1116	pertussis	semapv:ManualMappingCuration	2022-01-24
EFO:0000653	phyllodes tumor	skos:exactMatch	DOID:9004240	Phyllodes Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:0000658	plexiform neurofibroma	skos:exactMatch	DOID:5151	plexiform neurofibroma	semapv:ManualMappingCuration	2022-01-24
EFO:0000660	polycystic ovary syndrome	skos:exactMatch	DOID:11612	polycystic ovary syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0000662	polyp	skos:exactMatch	DOID:9003896	Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:0000666	portal hypertension	skos:exactMatch	DOID:10762	portal hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:0000668	preeclampsia	skos:exactMatch	DOID:10591	pre-eclampsia	semapv:ManualMappingCuration	2022-01-24
EFO:0000673	prostate adenocarcinoma	skos:exactMatch	DOID:2526	prostate adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000676	psoriasis	skos:exactMatch	DOID:8893	psoriasis	semapv:ManualMappingCuration	2022-01-24
EFO:0000677	mental or behavioural disorder	skos:exactMatch	DOID:150	disease of mental health	semapv:ManualMappingCuration	2022-01-24
EFO:0000677	mental or behavioural disorder	skos:exactMatch	DOID:2468	psychotic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0000678	pterygium	skos:exactMatch	DOID:0002116	pterygium	semapv:ManualMappingCuration	2022-01-24
EFO:0000681	renal cell carcinoma	skos:exactMatch	DOID:4450	renal cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000684	respiratory system disease	skos:exactMatch	DOID:1579	respiratory system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000685	rheumatoid arthritis	skos:exactMatch	DOID:7148	rheumatoid arthritis	semapv:ManualMappingCuration	2022-01-24
EFO:0000691	sarcoma	skos:exactMatch	DOID:1115	sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000693	schwannoma	skos:exactMatch	DOID:12689	acoustic neuroma	semapv:ManualMappingCuration	2022-01-24
EFO:0000693	schwannoma	skos:exactMatch	DOID:3192	neurilemmoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000693	schwannoma	skos:exactMatch	DOID:3196	cellular schwannoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000693	schwannoma	skos:exactMatch	DOID:3206	plexiform schwannoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000693	schwannoma	skos:exactMatch	DOID:955	benign neurilemmoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000694	severe acute respiratory syndrome	skos:exactMatch	DOID:2945	severe acute respiratory syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0000698	signet ring cell carcinoma	skos:exactMatch	DOID:3493	signet ring cell adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000699	Sjogren syndrome	skos:exactMatch	DOID:12894	Sjogren's syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0000699	Sjogren syndrome	skos:exactMatch	DOID:12900	Mikulicz disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000701	skin disease	skos:exactMatch	DOID:37	skin disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000702	small cell lung carcinoma	skos:exactMatch	DOID:5409	lung small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000702	small cell lung carcinoma	skos:exactMatch	DOID:5411	lung oat cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000705	spindle cell tumor	skos:exactMatch	DOID:9005456	spindle cell neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:0000706	spondyloarthropathy	skos:exactMatch	DOID:1123	spondyloarthropathy	semapv:ManualMappingCuration	2022-01-24
EFO:0000707	squamous cell carcinoma	skos:exactMatch	DOID:1749	squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000708	squamous cell lung carcinoma	skos:exactMatch	DOID:3907	lung squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000712	stroke	skos:exactMatch	DOID:9007096	Stroke	semapv:ManualMappingCuration	2023-12-04
EFO:0000713	subarachnoid hemorrhage	skos:exactMatch	DOID:9000438	Subarachnoid Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0000717	systemic scleroderma	skos:exactMatch	DOID:418	systemic scleroderma	semapv:ManualMappingCuration	2022-01-24
EFO:0000729	ulcerative colitis	skos:exactMatch	DOID:8577	ulcerative colitis	semapv:ManualMappingCuration	2022-01-24
EFO:0000730	undifferentiated sarcoma	skos:exactMatch	DOID:9006050	undifferentiated sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:0000731	uterine fibroid	skos:exactMatch	DOID:13223	uterine fibroid	semapv:ManualMappingCuration	2022-01-24
EFO:0000734	vitamin B12 deficiency	skos:exactMatch	DOID:0050731	vitamin B12 deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0000736	well-differentiated liposarcoma	skos:exactMatch	DOID:5690	well-differentiated liposarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:0000756	melanoma	skos:exactMatch	DOID:1909	melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000759	lipoma	skos:exactMatch	DOID:3315	lipoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000760	malignant peripheral nerve sheath tumor	skos:exactMatch	DOID:5940	malignant peripheral nerve sheath tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0000762	hepatocellular adenoma	skos:exactMatch	DOID:0050868	hepatocellular adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0000763	viral disease	skos:exactMatch	DOID:934	viral infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000764	HIV infection	skos:exactMatch	DOID:526	human immunodeficiency virus infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000765	AIDS	skos:exactMatch	DOID:635	acquired immunodeficiency syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0000767	idiopathic cardiomyopathy	skos:exactMatch	DOID:0050700	cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0000768	idiopathic pulmonary fibrosis	skos:exactMatch	DOID:0050156	idiopathic pulmonary fibrosis	semapv:ManualMappingCuration	2022-01-24
EFO:0000769	Epstein-Barr virus infection	skos:exactMatch	DOID:2938	Epstein-Barr virus infectious disease	semapv:ManualMappingCuration	2023-12-04
EFO:0000770	malignant pleural mesothelioma	skos:exactMatch	DOID:7474	malignant pleural mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:0000771	bacterial disease	skos:exactMatch	DOID:104	bacterial infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000772	pneumococcal infection	skos:exactMatch	DOID:9000989	Pneumococcal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0000773	temporal lobe epilepsy	skos:exactMatch	DOID:3328	temporal lobe epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:0000775	Whipple's disease	skos:exactMatch	DOID:8476	Whipple disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000777	human granulocytic anaplasmosis	skos:exactMatch	DOID:0050025	human granulocytic anaplasmosis	semapv:ManualMappingCuration	2022-01-24
EFO:0000778	anthrax infection	skos:exactMatch	DOID:7427	anthrax disease	semapv:ManualMappingCuration	2022-01-24
EFO:0000780	Enterococcus faecalis infection	skos:exactMatch	DOID:9002823	Gram-Positive Bacterial Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0000783	myositis	skos:exactMatch	DOID:633	myositis	semapv:ManualMappingCuration	2022-01-24
EFO:0001054	leprosy	skos:exactMatch	DOID:1024	leprosy	semapv:ManualMappingCuration	2022-01-24
EFO:0001055	borderline leprosy	skos:exactMatch	DOID:1023	borderline leprosy	semapv:ManualMappingCuration	2022-01-24
EFO:0001056	tuberculoid leprosy	skos:exactMatch	DOID:1025	tuberculoid leprosy	semapv:ManualMappingCuration	2022-01-24
EFO:0001057	lepromatous leprosy	skos:exactMatch	DOID:10887	lepromatous leprosy	semapv:ManualMappingCuration	2022-01-24
EFO:0001058	sensory system disease	skos:exactMatch	DOID:0050155	sensory system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0001060	celiac disease	skos:exactMatch	DOID:10608	celiac disease	semapv:ManualMappingCuration	2022-01-24
EFO:0001061	cervical carcinoma	skos:exactMatch	DOID:2893	cervix carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0001062	cytomegalovirus infection	skos:exactMatch	DOID:9006262	Cytomegalovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0001063	deafness	skos:exactMatch	DOID:9008681	Deafness	semapv:ManualMappingCuration	2023-12-04
EFO:0001064	Down syndrome	skos:exactMatch	DOID:14250	Down syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0001065	endometriosis	skos:exactMatch	DOID:289	endometriosis	semapv:ManualMappingCuration	2022-01-24
EFO:0001066	experimental autoimmune encephalomyelitis	skos:exactMatch	DOID:9002763	Experimental Autoimmune Encephalomyelitis	semapv:ManualMappingCuration	2023-12-04
EFO:0001067	parasitic infection	skos:exactMatch	DOID:1398	parasitic infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:0001068	malaria	skos:exactMatch	DOID:12365	malaria	semapv:ManualMappingCuration	2022-01-24
EFO:0001069	nutritional disorder	skos:exactMatch	DOID:374	nutrition disease	semapv:ManualMappingCuration	2022-01-24
EFO:0001070	folate deficiency	skos:exactMatch	DOID:14026	folic acid deficiency anemia	semapv:ManualMappingCuration	2023-12-04
EFO:0001071	lung carcinoma	skos:exactMatch	DOID:3905	lung carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0001072	memory impairment	skos:exactMatch	DOID:9008023	Memory Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0001073	obesity	skos:exactMatch	DOID:9970	obesity	semapv:ManualMappingCuration	2022-01-24
EFO:0001074	morbid obesity	skos:exactMatch	DOID:11981	morbid obesity	semapv:ManualMappingCuration	2022-01-24
EFO:0001075	ovarian carcinoma	skos:exactMatch	DOID:4001	ovarian carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0001076	Pseudomonas infection	skos:exactMatch	DOID:9007417	Pseudomonas Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0001077	Pseudomonas aeruginosa CF5 infection	skos:exactMatch	DOID:9007417	Pseudomonas Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0001356	familial amyotrophic lateral sclerosis	skos:exactMatch	DOID:332	amyotrophic lateral sclerosis	semapv:ManualMappingCuration	2023-12-04
EFO:0001357	sporadic amyotrophic lateral sclerosis	skos:exactMatch	DOID:0080917	sporadic amyotrophic lateral sclerosis	semapv:ManualMappingCuration	2023-04-17
EFO:0001357	sporadic amyotrophic lateral sclerosis	skos:exactMatch	DOID:332	amyotrophic lateral sclerosis	semapv:ManualMappingCuration	2023-12-04
EFO:0001358	post-traumatic stress disorder	skos:exactMatch	DOID:2055	post-traumatic stress disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0001361	pulmonary arterial hypertension	skos:exactMatch	DOID:6432	pulmonary hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:0001361	pulmonary arterial hypertension	skos:exactMatch	DOID:9001820	Pulmonary Arterial Hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0001365	age-related macular degeneration	skos:exactMatch	DOID:10871	age related macular degeneration	semapv:ManualMappingCuration	2022-01-24
EFO:0001365	age-related macular degeneration	skos:exactMatch	DOID:4448	macular degeneration	semapv:ManualMappingCuration	2022-01-24
EFO:0001376	synovial sarcoma	skos:exactMatch	DOID:5485	synovial sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0001378	multiple myeloma	skos:exactMatch	DOID:9538	multiple myeloma	semapv:ManualMappingCuration	2022-01-24
EFO:0001379	endocrine system disease	skos:exactMatch	DOID:28	endocrine system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0001380	hypopituitarism	skos:exactMatch	DOID:9406	hypopituitarism	semapv:ManualMappingCuration	2022-01-24
EFO:0001416	cervical adenocarcinoma	skos:exactMatch	DOID:3702	cervical adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0001421	liver disease	skos:exactMatch	DOID:409	liver disease	semapv:ManualMappingCuration	2022-01-24
EFO:0001422	cirrhosis of liver	skos:exactMatch	DOID:5082	liver cirrhosis	semapv:ManualMappingCuration	2022-01-24
EFO:0001423	encephalomyelitis	skos:exactMatch	DOID:640	encephalomyelitis	semapv:ManualMappingCuration	2022-01-24
EFO:0001425	ischemic cardiomyopathy	skos:exactMatch	DOID:9003511	ischemic cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0001645	coronary artery disease	skos:exactMatch	DOID:3393	coronary artery disease	semapv:ManualMappingCuration	2022-01-24
EFO:0001663	prostate carcinoma	skos:exactMatch	DOID:10286	prostate carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0001666	aortic aneurysm	skos:exactMatch	DOID:3627	aortic aneurysm	semapv:ManualMappingCuration	2022-01-24
EFO:0001668	human papilloma virus infection	skos:exactMatch	DOID:11166	papillomavirus infectious disease	semapv:ManualMappingCuration	2023-04-17
EFO:0002087	fibrosarcoma	skos:exactMatch	DOID:3355	fibrosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002422	benign neoplasm	skos:exactMatch	DOID:0060072	benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0002422	benign neoplasm	skos:exactMatch	DOID:0060084	cell type benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0002422	benign neoplasm	skos:exactMatch	DOID:0060085	organ system benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0002423	osteoma	skos:exactMatch	DOID:9004412	Osteoma	semapv:ManualMappingCuration	2023-12-04
EFO:0002424	fibroma	skos:exactMatch	DOID:0050871	fibroma	semapv:ManualMappingCuration	2022-01-24
EFO:0002427	myeloid neoplasm	skos:exactMatch	DOID:0070004	myeloid neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0002428	chronic myeloproliferative disorder	skos:exactMatch	DOID:2226	myeloproliferative neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0002429	polycythemia vera	skos:exactMatch	DOID:8997	polycythemia vera	semapv:ManualMappingCuration	2022-01-24
EFO:0002430	primary myelofibrosis	skos:exactMatch	DOID:4971	myelofibrosis	semapv:ManualMappingCuration	2022-01-24
EFO:0002431	tumour of cranial and spinal nerves	skos:exactMatch	DOID:1192	peripheral nervous system neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0002460	hypertrophy	skos:exactMatch	DOID:9000040	Hypertrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0002496	actinic keratosis	skos:exactMatch	DOID:8866	actinic keratosis	semapv:ManualMappingCuration	2022-01-24
EFO:0002498	aggressive insulitis	skos:exactMatch	DOID:4989	pancreatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0002499	anaplastic astrocytoma	skos:exactMatch	DOID:3078	anaplastic astrocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002500	anaplastic oligoastrocytoma	skos:exactMatch	DOID:3069	malignant astrocytoma	semapv:ManualMappingCuration	2023-12-04
EFO:0002501	anaplastic oligodendroglioma	skos:exactMatch	DOID:7154	anaplastic oligodendroglioma	semapv:ManualMappingCuration	2023-03-17
EFO:0002502	benign insulitis	skos:exactMatch	DOID:4989	pancreatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0002503	cardiac hypertrophy	skos:exactMatch	DOID:9003936	Cardiomegaly	semapv:ManualMappingCuration	2023-12-04
EFO:0002504	serous cystadenoma	skos:exactMatch	DOID:9008844	Serous Cystadenoma	semapv:ManualMappingCuration	2023-12-04
EFO:0002507	ovarian adenoma benign	skos:exactMatch	DOID:0060112	ovarian benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:0002509	progressive external ophthalmoplegia	skos:exactMatch	DOID:12558	chronic progressive external ophthalmoplegia	semapv:ManualMappingCuration	2022-01-24
EFO:0002511	simple cystadenoma	skos:exactMatch	DOID:3269	ovarian cystadenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002608	AIDS dementia	skos:exactMatch	DOID:9004086	AIDS Dementia Complex	semapv:ManualMappingCuration	2023-12-04
EFO:0002609	juvenile idiopathic arthritis	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2022-01-24
EFO:0002610	cocaine dependence	skos:exactMatch	DOID:9975	cocaine dependence	semapv:ManualMappingCuration	2022-01-24
EFO:0002612	human herpesvirus 8 infection	skos:exactMatch	DOID:9007812	human herpesvirus 8 infection	semapv:ManualMappingCuration	2023-12-04
EFO:0002613	iatrogenic Kaposi's sarcoma	skos:exactMatch	DOID:8632	Kaposi's sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:0002614	insulin resistance	skos:exactMatch	DOID:9007692	Insulin Resistance	semapv:ManualMappingCuration	2023-12-04
EFO:0002615	internal carotid artery stenosis	skos:exactMatch	DOID:13001	carotid stenosis	semapv:ManualMappingCuration	2023-12-04
EFO:0002616	macroglobulinemia	skos:exactMatch	DOID:9080	macroglobulinemia	semapv:ManualMappingCuration	2022-01-24
EFO:0002618	pancreatic carcinoma	skos:exactMatch	DOID:4905	pancreatic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002621	prostate intraepithelial neoplasia	skos:exactMatch	DOID:8634	prostate carcinoma in situ	semapv:ManualMappingCuration	2023-12-04
EFO:0002622	rotavirus infection	skos:exactMatch	DOID:9000645	Rotavirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0002623	septic peritonitis	skos:exactMatch	DOID:9007367	Septic Peritonitis	semapv:ManualMappingCuration	2023-12-04
EFO:0002626	thymus neoplasm	skos:exactMatch	DOID:9005161	Thymus Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0002627	vulvar intraepithelial neoplasia	skos:exactMatch	DOID:9006454	vulvar intraepithelial neoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0002628	peripartum cardiomyopathy	skos:exactMatch	DOID:9997	peripartum cardiomyopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0002629	viral cardiomyopathy	skos:exactMatch	DOID:0050700	cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0002630	restrictive cardiomyopathy	skos:exactMatch	DOID:397	restrictive cardiomyopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0002687	ischemia reperfusion injury	skos:exactMatch	DOID:9004009	Reperfusion Injury	semapv:ManualMappingCuration	2023-12-04
EFO:0002689	antiphospholipid syndrome	skos:exactMatch	DOID:2988	antiphospholipid syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0002890	renal carcinoma	skos:exactMatch	DOID:4451	renal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002892	thyroid carcinoma	skos:exactMatch	DOID:3963	thyroid gland carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002893	choriocarcinoma	skos:exactMatch	DOID:3594	choriocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002894	amelanotic skin melanoma	skos:exactMatch	DOID:10054	skin amelanotic melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002913	Cutaneous T-cell lymphoma	skos:exactMatch	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002914	uterine sarcoma	skos:exactMatch	DOID:5165	uterine corpus sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002916	esophageal carcinoma	skos:exactMatch	DOID:1107	esophageal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002917	ovarian serous adenocarcinoma	skos:exactMatch	DOID:0050933	ovarian serous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002917	ovarian serous adenocarcinoma	skos:exactMatch	DOID:5744	ovary serous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002918	rhabdomyosarcoma	skos:exactMatch	DOID:3247	rhabdomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002919	uterine carcinoma	skos:exactMatch	DOID:9008198	uterine carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0002920	vulva sarcoma	skos:exactMatch	DOID:2096	vulvar sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002921	vulvar carcinoma	skos:exactMatch	DOID:1294	vulva carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002938	hypopharyngeal carcinoma	skos:exactMatch	DOID:8533	hypopharynx cancer	semapv:ManualMappingCuration	2023-12-04
EFO:0002939	medulloblastoma	skos:exactMatch	DOID:0050902	medulloblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002939	medulloblastoma	skos:exactMatch	DOID:0060104	cerebellar medulloblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0002945	familial cardiomyopathy	skos:exactMatch	DOID:0050700	cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0002970	muscular disease	skos:exactMatch	DOID:0080000	muscular disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003014	breast fibrocystic disease	skos:exactMatch	DOID:10354	breast fibrocystic disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003016	collecting duct carcinoma	skos:exactMatch	DOID:4464	collecting duct carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003017	transitional cell carcinoma of kidney	skos:exactMatch	DOID:5974	renal pelvis transitional cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003025	acute megakaryoblastic leukaemia	skos:exactMatch	DOID:8761	acute megakaryocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0003026	minimally differentiated acute myeloblastic leukemia	skos:exactMatch	DOID:0081085	acute myeloid leukemia with minimal differentiation	semapv:ManualMappingCuration	2023-03-17
EFO:0003027	acute myeloblastic leukemia without maturation	skos:exactMatch	DOID:0081086	acute myeloid leukemia without maturation	semapv:ManualMappingCuration	2023-04-17
EFO:0003028	acute myeloblastic leukemia with maturation	skos:exactMatch	DOID:0081087	acute myeloid leukemia with maturation	semapv:ManualMappingCuration	2023-04-17
EFO:0003029	acute basophilic leukemia	skos:exactMatch	DOID:0080795	acute basophilic leukemia	semapv:ManualMappingCuration	2023-03-17
EFO:0003030	abscess	skos:exactMatch	DOID:9000325	Abscess	semapv:ManualMappingCuration	2023-12-04
EFO:0003032	anaplastic large cell lymphoma	skos:exactMatch	DOID:0050744	anaplastic large cell lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003033	bacteriemia	skos:exactMatch	DOID:0040085	bacterial sepsis	semapv:ManualMappingCuration	2022-01-24
EFO:0003033	bacteriemia	skos:exactMatch	DOID:9005036	Bacteremia	semapv:ManualMappingCuration	2023-12-04
EFO:0003035	cellulitis	skos:exactMatch	DOID:3488	cellulitis	semapv:ManualMappingCuration	2022-01-24
EFO:0003046	heart transplant rejection	skos:exactMatch	DOID:9005298	heart transplant rejection	semapv:ManualMappingCuration	2023-12-04
EFO:0003047	hepatitis C virus infection	skos:exactMatch	DOID:1883	hepatitis C	semapv:ManualMappingCuration	2022-01-24
EFO:0003050	large cell lung carcinoma	skos:exactMatch	DOID:4556	lung large cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003060	non-small cell lung carcinoma	skos:exactMatch	DOID:3908	lung non-small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003063	polymyositis	skos:exactMatch	DOID:0080745	polymyositis	semapv:ManualMappingCuration	2023-03-17
EFO:0003073	asymptomatic myeloma	skos:exactMatch	DOID:9551	smoldering myeloma	semapv:ManualMappingCuration	2022-01-24
EFO:0003075	xanthoma	skos:exactMatch	DOID:3345	xanthomatosis	semapv:ManualMappingCuration	2023-12-04
EFO:0003083	pleomorphic liposarcoma	skos:exactMatch	DOID:5702	pleomorphic liposarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003084	round cell liposarcoma	skos:exactMatch	DOID:5692	cellular myxoid liposarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003085	dedifferentiated liposarcoma	skos:exactMatch	DOID:0080531	dedifferentiated liposarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003086	kidney disease	skos:exactMatch	DOID:557	kidney disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003094	ganglioglioma	skos:exactMatch	DOID:5078	ganglioglioma	semapv:ManualMappingCuration	2022-01-24
EFO:0003095	non-alcoholic fatty liver disease	skos:exactMatch	DOID:0080208	metabolic dysfunction-associated steatotic liver disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003095	non-alcoholic fatty liver disease	skos:exactMatch	DOID:0080546	non-alcoholic fatty liver	semapv:ManualMappingCuration	2023-04-17
EFO:0003096	Pick disease	skos:exactMatch	DOID:11870	Pick's disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003097	empyema	skos:exactMatch	DOID:9004425	Empyema	semapv:ManualMappingCuration	2023-12-04
EFO:0003099	Cushing syndrome	skos:exactMatch	DOID:9005158	Cushing Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0003100	peripheral neuropathy	skos:exactMatch	DOID:870	neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:0003101	testicular seminoma	skos:exactMatch	DOID:5842	testis seminoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003102	osteomyelitis	skos:exactMatch	DOID:1019	osteomyelitis	semapv:ManualMappingCuration	2022-01-24
EFO:0003103	urinary tract infection	skos:exactMatch	DOID:0080784	urinary tract infection	semapv:ManualMappingCuration	2023-03-17
EFO:0003104	adrenocortical adenoma	skos:exactMatch	DOID:0050891	adrenal cortical adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003104	adrenocortical adenoma	skos:exactMatch	DOID:656	adrenal adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003105	spina bifida	skos:exactMatch	DOID:0080016	spina bifida	semapv:ManualMappingCuration	2022-01-24
EFO:0003106	pneumonia	skos:exactMatch	DOID:552	pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:0003108	essential tremor	skos:exactMatch	DOID:4990	essential tremor	semapv:ManualMappingCuration	2022-01-24
EFO:0003110	villitis	skos:exactMatch	DOID:9002556	villitis	semapv:ManualMappingCuration	2023-12-04
EFO:0003144	heart failure	skos:exactMatch	DOID:6000	congestive heart failure	semapv:ManualMappingCuration	2023-12-04
EFO:0003145	high output heart failure	skos:exactMatch	DOID:6000	congestive heart failure	semapv:ManualMappingCuration	2023-12-04
EFO:0003146	symptomatic heart failure	skos:exactMatch	DOID:6000	congestive heart failure	semapv:ManualMappingCuration	2023-12-04
EFO:0003148	moderate heart failure	skos:exactMatch	DOID:6000	congestive heart failure	semapv:ManualMappingCuration	2023-12-04
EFO:0003149	advanced heart failure	skos:exactMatch	DOID:6000	congestive heart failure	semapv:ManualMappingCuration	2023-12-04
EFO:0003756	autism spectrum disorder	skos:exactMatch	DOID:0060041	autism spectrum disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0003757	Asperger syndrome	skos:exactMatch	DOID:0050432	Asperger syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0003758	autism	skos:exactMatch	DOID:12849	autistic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0003759	pervasive developmental disorder - not otherwise specified	skos:exactMatch	DOID:0060042	atypical autism	semapv:ManualMappingCuration	2022-01-24
EFO:0003760	central nervous system cyst	skos:exactMatch	DOID:9003857	Central Nervous System Cysts	semapv:ManualMappingCuration	2023-12-04
EFO:0003762	vitamin D deficiency	skos:exactMatch	DOID:9006359	Vitamin D Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0003763	cerebrovascular disorder	skos:exactMatch	DOID:6713	cerebrovascular disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003764	transient ischemic attack	skos:exactMatch	DOID:224	transient cerebral ischemia	semapv:ManualMappingCuration	2022-01-24
EFO:0003765	sign or symptom	skos:exactMatch	DOID:9000071	Signs and Symptoms	semapv:ManualMappingCuration	2023-12-04
EFO:0003767	inflammatory bowel disease	skos:exactMatch	DOID:0050589	inflammatory bowel disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003768	nicotine dependence	skos:exactMatch	DOID:0050742	nicotine dependence	semapv:ManualMappingCuration	2022-01-24
EFO:0003769	endocrine neoplasm	skos:exactMatch	DOID:170	endocrine gland cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003769	endocrine neoplasm	skos:exactMatch	DOID:9007803	Endocrine Gland Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003770	diabetic retinopathy	skos:exactMatch	DOID:8947	diabetic retinopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0003777	heart disease	skos:exactMatch	DOID:114	heart disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003778	psoriatic arthritis	skos:exactMatch	DOID:9008	psoriatic arthritis	semapv:ManualMappingCuration	2022-01-24
EFO:0003779	Hashimoto's thyroiditis	skos:exactMatch	DOID:7188	autoimmune thyroiditis	semapv:ManualMappingCuration	2022-01-24
EFO:0003779	Hashimoto's thyroiditis	skos:exactMatch	DOID:9007355	Hashimoto Disease	semapv:ManualMappingCuration	2023-12-04
EFO:0003780	Behcet's syndrome	skos:exactMatch	DOID:13241	Behcet's disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003781	carotid artery disease	skos:exactMatch	DOID:3407	carotid artery disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003782	motor neuron disease	skos:exactMatch	DOID:231	motor neuron disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003783	progressive bulbar palsy	skos:exactMatch	DOID:681	progressive bulbar palsy	semapv:ManualMappingCuration	2022-01-24
EFO:0003802	refractory anemia	skos:exactMatch	DOID:9000300	Refractory Anemia	semapv:ManualMappingCuration	2023-12-04
EFO:0003811	refractory anemia with excess blasts	skos:exactMatch	DOID:9005969	Refractory Anemia with Excess of Blasts	semapv:ManualMappingCuration	2023-12-04
EFO:0003812	refractory anemia with ringed sideroblasts	skos:exactMatch	DOID:8955	sideroblastic anemia	semapv:ManualMappingCuration	2023-12-04
EFO:0003817	laryngeal neoplasm	skos:exactMatch	DOID:2596	larynx cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003817	laryngeal neoplasm	skos:exactMatch	DOID:9003613	Laryngeal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003818	lung disease	skos:exactMatch	DOID:850	lung disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003819	dental caries	skos:exactMatch	DOID:216	dental caries	semapv:ManualMappingCuration	2022-01-24
EFO:0003820	bone neoplasm	skos:exactMatch	DOID:184	bone cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003820	bone neoplasm	skos:exactMatch	DOID:9004389	Bone Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003822	hyperemia	skos:exactMatch	DOID:9009039	Hyperemia	semapv:ManualMappingCuration	2023-12-04
EFO:0003824	eye neoplasm	skos:exactMatch	DOID:9004059	Eye Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003825	serous adenocarcinoma	skos:exactMatch	DOID:3114	serous cystadenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003826	salivary gland neoplasm	skos:exactMatch	DOID:8850	salivary gland cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003826	salivary gland neoplasm	skos:exactMatch	DOID:9003216	Salivary Gland Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003827	pulmonary embolism	skos:exactMatch	DOID:9477	pulmonary embolism	semapv:ManualMappingCuration	2022-01-24
EFO:0003828	spinal cord neoplasm	skos:exactMatch	DOID:9006391	Spinal Cord Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003830	prostatitis	skos:exactMatch	DOID:14654	prostatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0003832	gallbladder disease	skos:exactMatch	DOID:0060262	gallbladder disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003833	brain neoplasm	skos:exactMatch	DOID:1319	brain cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003833	brain neoplasm	skos:exactMatch	DOID:9007502	Brain Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003834	cutaneous lupus erythematosus	skos:exactMatch	DOID:0050169	cutaneous lupus erythematosus	semapv:ManualMappingCuration	2022-01-24
EFO:0003835	anal neoplasm	skos:exactMatch	DOID:14110	anus cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003835	anal neoplasm	skos:exactMatch	DOID:4551	anus benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0003837	calcification	skos:exactMatch	DOID:182	calcinosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003839	retinopathy	skos:exactMatch	DOID:5679	retinal disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003840	chronic progressive multiple sclerosis	skos:exactMatch	DOID:0050783	secondary progressive multiple sclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003840	chronic progressive multiple sclerosis	skos:exactMatch	DOID:0050784	primary progressive multiple sclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003840	chronic progressive multiple sclerosis	skos:exactMatch	DOID:0050785	progressive relapsing multiple sclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003841	thyroid neoplasm	skos:exactMatch	DOID:2891	thyroid adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0003841	thyroid neoplasm	skos:exactMatch	DOID:9004547	Thyroid Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003843	pain	skos:exactMatch	DOID:9000641	Pain	semapv:ManualMappingCuration	2023-12-04
EFO:0003844	ureteral neoplasm	skos:exactMatch	DOID:11819	ureter cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003844	ureteral neoplasm	skos:exactMatch	DOID:9003753	Ureteral Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003846	urethral neoplasm	skos:exactMatch	DOID:734	urethra cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003846	urethral neoplasm	skos:exactMatch	DOID:9002378	Urethral Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003849	palatal neoplasm	skos:exactMatch	DOID:9005313	Palatal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003850	adrenal gland neoplasm	skos:exactMatch	DOID:3953	adrenal gland cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003850	adrenal gland neoplasm	skos:exactMatch	DOID:9000362	Adrenal Gland Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003851	meningeal neoplasm	skos:exactMatch	DOID:9007166	Meningeal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003852	developmental disability	skos:exactMatch	DOID:9008086	Developmental Disabilities	semapv:ManualMappingCuration	2023-12-04
EFO:0003853	respiratory system neoplasm	skos:exactMatch	DOID:9003744	Respiratory Tract Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003854	postmenopausal osteoporosis	skos:exactMatch	DOID:9004914	Postmenopausal Osteoporosis	semapv:ManualMappingCuration	2023-12-04
EFO:0003855	intestinal polyp	skos:exactMatch	DOID:9001642	Intestinal Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:0003857	arthrogryposis	skos:exactMatch	DOID:0080954	arthrogryposis multiplex congenita	semapv:ManualMappingCuration	2023-12-04
EFO:0003859	uterine neoplasm	skos:exactMatch	DOID:363	uterine cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003859	uterine neoplasm	skos:exactMatch	DOID:9004268	Uterine Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003860	pancreatic neoplasm	skos:exactMatch	DOID:1793	pancreatic cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003860	pancreatic neoplasm	skos:exactMatch	DOID:9003100	Pancreatic Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003863	urogenital neoplasm	skos:exactMatch	DOID:9007150	Urogenital Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003865	kidney neoplasm	skos:exactMatch	DOID:263	kidney cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003865	kidney neoplasm	skos:exactMatch	DOID:9002265	Kidney Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003866	paranasal sinus neoplasm	skos:exactMatch	DOID:1350	paranasal sinus benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0003867	rhabdomyolysis	skos:exactMatch	DOID:9000884	Rhabdomyolysis	semapv:ManualMappingCuration	2023-12-04
EFO:0003868	mouth neoplasm	skos:exactMatch	DOID:9007364	Mouth Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003869	breast neoplasm	skos:exactMatch	DOID:9008939	Breast Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003870	brain aneurysm	skos:exactMatch	DOID:10941	intracranial aneurysm	semapv:ManualMappingCuration	2022-01-24
EFO:0003871	tongue neoplasm	skos:exactMatch	DOID:8649	tongue cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003871	tongue neoplasm	skos:exactMatch	DOID:9005873	Tongue Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003872	colitis	skos:exactMatch	DOID:0060180	colitis	semapv:ManualMappingCuration	2022-01-24
EFO:0003873	parotid neoplasm	skos:exactMatch	DOID:9000769	Parotid Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003874	flatfoot	skos:exactMatch	DOID:9007573	Flatfoot	semapv:ManualMappingCuration	2023-12-04
EFO:0003875	peripheral vascular disease	skos:exactMatch	DOID:341	peripheral vascular disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003876	intermittent vascular claudication	skos:exactMatch	DOID:3669	intermittent claudication	semapv:ManualMappingCuration	2022-01-24
EFO:0003877	sleep apnea	skos:exactMatch	DOID:0050847	sleep apnea	semapv:ManualMappingCuration	2022-01-24
EFO:0003878	urethritis	skos:exactMatch	DOID:1343	urethritis	semapv:ManualMappingCuration	2022-01-24
EFO:0003880	appendiceal neoplasm	skos:exactMatch	DOID:11240	appendiceal neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0003882	osteoporosis	skos:exactMatch	DOID:11476	osteoporosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003884	chronic kidney disease	skos:exactMatch	DOID:784	chronic kidney disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003888	attention deficit hyperactivity disorder	skos:exactMatch	DOID:1094	attention deficit hyperactivity disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0003890	drug dependence	skos:exactMatch	DOID:9974	drug dependence	semapv:ManualMappingCuration	2022-01-24
EFO:0003891	biliary tract neoplasm	skos:exactMatch	DOID:0050625	biliary tract benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0003893	ovarian neoplasm	skos:exactMatch	DOID:9002762	Ovarian Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003894	acne	skos:exactMatch	DOID:6543	acne	semapv:ManualMappingCuration	2022-01-24
EFO:0003895	epistaxis	skos:exactMatch	DOID:9008421	Epistaxis	semapv:ManualMappingCuration	2023-12-04
EFO:0003896	left ventricular hypertrophy	skos:exactMatch	DOID:9004616	Left Ventricular Hypertrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0003897	stomach neoplasm	skos:exactMatch	DOID:10534	stomach cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0003897	stomach neoplasm	skos:exactMatch	DOID:9000217	Stomach Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0003898	ankylosing spondylitis	skos:exactMatch	DOID:7147	ankylosing spondylitis	semapv:ManualMappingCuration	2022-01-24
EFO:0003899	contracture	skos:exactMatch	DOID:9006836	Contracture	semapv:ManualMappingCuration	2023-12-04
EFO:0003900	ciliopathy	skos:exactMatch	DOID:0060340	ciliopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0003901	dysuria	skos:exactMatch	DOID:9006846	Dysuria	semapv:ManualMappingCuration	2023-12-04
EFO:0003902	spinal fracture	skos:exactMatch	DOID:9002407	Spinal Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0003907	deep vein thrombosis	skos:exactMatch	DOID:9003871	Venous Thrombosis	semapv:ManualMappingCuration	2023-12-04
EFO:0003911	atrial flutter	skos:exactMatch	DOID:9003901	Atrial Flutter	semapv:ManualMappingCuration	2023-12-04
EFO:0003913	angina pectoris	skos:exactMatch	DOID:9000483	Angina Pectoris	semapv:ManualMappingCuration	2023-12-04
EFO:0003914	atherosclerosis	skos:exactMatch	DOID:1936	atherosclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003917	premature birth	skos:exactMatch	DOID:9003507	Premature Birth	semapv:ManualMappingCuration	2023-12-04
EFO:0003918	obstructive sleep apnea	skos:exactMatch	DOID:0050848	obstructive sleep apnea	semapv:ManualMappingCuration	2022-01-24
EFO:0003921	pouchitis	skos:exactMatch	DOID:9006064	Pouchitis	semapv:ManualMappingCuration	2023-12-04
EFO:0003928	necrotizing enterocolitis	skos:exactMatch	DOID:8677	perinatal necrotizing enterocolitis	semapv:ManualMappingCuration	2023-12-04
EFO:0003929	relapsing-remitting multiple sclerosis	skos:exactMatch	DOID:2378	relapsing-remitting multiple sclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003931	bone fracture	skos:exactMatch	DOID:9002589	Bone Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0003932	bacterial vaginosis	skos:exactMatch	DOID:3385	bacterial vaginosis	semapv:ManualMappingCuration	2022-01-24
EFO:0003938	aphthous ulcer	skos:exactMatch	DOID:9663	aphthous stomatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0003943	humerus fracture	skos:exactMatch	DOID:9000529	Humeral Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0003944	tibia fracture	skos:exactMatch	DOID:9001547	Tibial Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0003948	gastroesophageal reflux disease	skos:exactMatch	DOID:8534	gastroesophageal reflux disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003950	ulna fracture	skos:exactMatch	DOID:9001872	Ulna Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0003952	fever of unknown origin	skos:exactMatch	DOID:9006865	Fever of Unknown Origin	semapv:ManualMappingCuration	2023-12-04
EFO:0003955	bacterial sexually transmitted disease	skos:exactMatch	DOID:9006980	Bacterial Sexually Transmitted Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0003956	seasonal allergic rhinitis	skos:exactMatch	DOID:9008103	Seasonal Allergic Rhinitis	semapv:ManualMappingCuration	2023-12-04
EFO:0003957	radius fracture	skos:exactMatch	DOID:9005316	Radius Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0003958	sunburn	skos:exactMatch	DOID:9003386	Sunburn	semapv:ManualMappingCuration	2023-12-04
EFO:0003959	cleft lip	skos:exactMatch	DOID:9296	cleft lip	semapv:ManualMappingCuration	2022-01-24
EFO:0003963	freckles	skos:exactMatch	DOID:9001583	Melanosis	semapv:ManualMappingCuration	2023-12-04
EFO:0003964	hip fracture	skos:exactMatch	DOID:9007265	Hip Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0003966	eye disease	skos:exactMatch	DOID:1242	globe disease	semapv:ManualMappingCuration	2023-03-06
EFO:0003966	eye disease	skos:exactMatch	DOID:5614	eye disease	semapv:ManualMappingCuration	2022-01-24
EFO:0003967	vascular sarcoma	skos:exactMatch	DOID:0001816	angiosarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:0003968	angiosarcoma	skos:exactMatch	DOID:0001816	angiosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0004125	growth hormone-secreting pituitary adenoma	skos:exactMatch	DOID:6255	growth hormone secreting pituitary adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:0004126	Adie syndrome	skos:exactMatch	DOID:11549	Adie syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004127	hyperthyroxinemia	skos:exactMatch	DOID:2855	hyperthyroxinemia	semapv:ManualMappingCuration	2022-01-24
EFO:0004128	hereditary nephritis	skos:exactMatch	DOID:10983	Alport syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0004129	familial amyloid neuropathy	skos:exactMatch	DOID:0050638	transthyretin amyloidosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004138	bundle branch block	skos:exactMatch	DOID:9003912	Bundle-Branch Block	semapv:ManualMappingCuration	2023-12-04
EFO:0004142	colorectal neoplasm	skos:exactMatch	DOID:9008443	Colorectal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004143	carpal tunnel syndrome	skos:exactMatch	DOID:12169	carpal tunnel syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004144	acatalasia	skos:exactMatch	DOID:2582	acatalasia	semapv:ManualMappingCuration	2022-01-24
EFO:0004145	myopathy	skos:exactMatch	DOID:423	myopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0004149	neuropathy	skos:exactMatch	DOID:870	neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:0004152	chorea	skos:exactMatch	DOID:12859	choreatic disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004190	open-angle glaucoma	skos:exactMatch	DOID:1067	open-angle glaucoma	semapv:ManualMappingCuration	2022-01-24
EFO:0004191	androgenetic alopecia	skos:exactMatch	DOID:0050801	androgenic alopecia	semapv:ManualMappingCuration	2022-01-24
EFO:0004192	alopecia areata	skos:exactMatch	DOID:986	alopecia areata	semapv:ManualMappingCuration	2022-01-24
EFO:0004193	basal cell carcinoma	skos:exactMatch	DOID:2513	basal cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0004194	IGA glomerulonephritis	skos:exactMatch	DOID:2986	IgA glomerulonephritis	semapv:ManualMappingCuration	2022-01-24
EFO:0004196	viral human hepatitis infection	skos:exactMatch	DOID:1884	viral hepatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0004196	viral human hepatitis infection	skos:exactMatch	DOID:9007329	Human Viral Hepatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0004197	hepatitis B virus infection	skos:exactMatch	DOID:2043	hepatitis B	semapv:ManualMappingCuration	2022-01-24
EFO:0004198	skin neoplasm	skos:exactMatch	DOID:3165	skin benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0004198	skin neoplasm	skos:exactMatch	DOID:4159	skin cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0004198	skin neoplasm	skos:exactMatch	DOID:9004464	Skin Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004199	dysplastic nevus	skos:exactMatch	DOID:10041	dysplastic nevus syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004200	Illumina Genome Analyzer	skos:exactMatch	DOID:9002969	Nevus	semapv:ManualMappingCuration	2023-12-04
EFO:0004207	pathological myopia	skos:exactMatch	DOID:11829	degenerative myopia	semapv:ManualMappingCuration	2022-01-24
EFO:0004208	Vitiligo	skos:exactMatch	DOID:12306	vitiligo	semapv:ManualMappingCuration	2022-01-24
EFO:0004209	hypospadias	skos:exactMatch	DOID:10892	hypospadias	semapv:ManualMappingCuration	2022-01-24
EFO:0004210	gallstones	skos:exactMatch	DOID:9006113	Gallstones	semapv:ManualMappingCuration	2023-12-04
EFO:0004211	Hypertriglyceridemia	skos:exactMatch	DOID:9006599	Hypertriglyceridemia	semapv:ManualMappingCuration	2023-12-04
EFO:0004212	Keloid	skos:exactMatch	DOID:9000058	Keloid	semapv:ManualMappingCuration	2023-12-04
EFO:0004213	otosclerosis	skos:exactMatch	DOID:12185	otosclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004214	Abdominal Aortic Aneurysm	skos:exactMatch	DOID:7693	abdominal aortic aneurysm	semapv:ManualMappingCuration	2022-01-24
EFO:0004216	conduct disorder	skos:exactMatch	DOID:12995	conduct disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0004220	chronic hepatitis C virus infection	skos:exactMatch	DOID:9004017	Chronic Hepatitis C	semapv:ManualMappingCuration	2023-12-04
EFO:0004224	Coronary Restenosis	skos:exactMatch	DOID:4247	coronary restenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004225	Coronary Vasospasm	skos:exactMatch	DOID:11840	coronary artery vasospasm	semapv:ManualMappingCuration	2022-01-24
EFO:0004226	Creutzfeldt Jacob Disease	skos:exactMatch	DOID:11949	Creutzfeldt-Jakob disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004227	Dengue Hemorrhagic Fever	skos:exactMatch	DOID:12206	dengue hemorrhagic fever	semapv:ManualMappingCuration	2022-01-24
EFO:0004228	drug-induced liver injury	skos:exactMatch	DOID:9007383	Chemical and Drug Induced Liver Injury	semapv:ManualMappingCuration	2023-12-04
EFO:0004229	Dupuytren Contracture	skos:exactMatch	DOID:9003793	Dupuytren Contracture	semapv:ManualMappingCuration	2023-12-04
EFO:0004230	endometrial neoplasm	skos:exactMatch	DOID:1380	endometrial cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0004230	endometrial neoplasm	skos:exactMatch	DOID:2871	endometrial carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0004230	endometrial neoplasm	skos:exactMatch	DOID:9007715	Endometrial Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004232	eosinophilic esophagitis	skos:exactMatch	DOID:13922	eosinophilic esophagitis	semapv:ManualMappingCuration	2022-01-24
EFO:0004233	leukopenia	skos:exactMatch	DOID:615	leukopenia	semapv:ManualMappingCuration	2022-01-24
EFO:0004234	erectile dysfunction	skos:exactMatch	DOID:1875	impotence	semapv:ManualMappingCuration	2022-01-24
EFO:0004235	exfoliation syndrome	skos:exactMatch	DOID:13641	exfoliation syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004236	focal segmental glomerulosclerosis	skos:exactMatch	DOID:1312	focal segmental glomerulosclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004237	Graves disease	skos:exactMatch	DOID:10719	toxic diffuse goiter	semapv:ManualMappingCuration	2022-01-24
EFO:0004237	Graves disease	skos:exactMatch	DOID:12361	Graves' disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004238	hearing loss	skos:exactMatch	DOID:9004538	Hearing Loss	semapv:ManualMappingCuration	2023-12-04
EFO:0004240	heroin dependence	skos:exactMatch	DOID:9976	heroin dependence	semapv:ManualMappingCuration	2022-01-24
EFO:0004242	obsessive-compulsive disorder	skos:exactMatch	DOID:10933	obsessive-compulsive disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0004243	carcinoid tumor	skos:exactMatch	DOID:9007787	Carcinoid Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:0004244	interstitial lung disease	skos:exactMatch	DOID:3082	interstitial lung disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004246	mucocutaneous lymph node syndrome	skos:exactMatch	DOID:13378	Kawasaki disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004247	mood disorder	skos:exactMatch	DOID:3324	mood disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0004248	male infertility	skos:exactMatch	DOID:12336	male infertility	semapv:ManualMappingCuration	2022-01-24
EFO:0004249	meningococcal infection	skos:exactMatch	DOID:9008366	Meningococcal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0004251	myeloproliferative disorder	skos:exactMatch	DOID:2226	myeloproliferative neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0004252	nasopharyngeal neoplasm	skos:exactMatch	DOID:9005207	Nasopharyngeal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004253	nephrolithiasis	skos:exactMatch	DOID:585	nephrolithiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0004254	membranous glomerulonephritis	skos:exactMatch	DOID:10976	membranous glomerulonephritis	semapv:ManualMappingCuration	2022-01-24
EFO:0004255	nephrotic syndrome	skos:exactMatch	DOID:1184	nephrotic syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004256	neuromyelitis optica	skos:exactMatch	DOID:8869	neuromyelitis optica	semapv:ManualMappingCuration	2022-01-24
EFO:0004257	neurotic disorder	skos:exactMatch	DOID:4964	neurotic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0004259	osteonecrosis	skos:exactMatch	DOID:0080008	ischemic bone disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004259	osteonecrosis	skos:exactMatch	DOID:10159	osteonecrosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004260	bone disease	skos:exactMatch	DOID:0080001	bone disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004261	osteitis deformans	skos:exactMatch	DOID:5408	Paget's disease of bone	semapv:ManualMappingCuration	2022-01-24
EFO:0004262	panic disorder	skos:exactMatch	DOID:594	panic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0004263	partial epilepsy	skos:exactMatch	DOID:2234	focal epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:0004264	vascular disease	skos:exactMatch	DOID:178	vascular disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004265	peripheral arterial disease	skos:exactMatch	DOID:0050830	peripheral artery disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004266	primary ovarian insufficiency	skos:exactMatch	DOID:5426	primary ovarian insufficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0004267	biliary liver cirrhosis	skos:exactMatch	DOID:12236	primary biliary cholangitis	semapv:ManualMappingCuration	2023-12-04
EFO:0004268	sclerosing cholangitis	skos:exactMatch	DOID:14268	sclerosing cholangitis	semapv:ManualMappingCuration	2022-01-24
EFO:0004269	cardiac arrhythmia	skos:exactMatch	DOID:9000064	Cardiac Arrhythmias	semapv:ManualMappingCuration	2023-12-04
EFO:0004270	restless legs syndrome	skos:exactMatch	DOID:0050425	restless legs syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004272	anemia (phenotype)	skos:exactMatch	DOID:2355	anemia	semapv:ManualMappingCuration	2022-01-24
EFO:0004273	scoliosis	skos:exactMatch	DOID:0060249	scoliosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004274	gout	skos:exactMatch	DOID:13189	gout	semapv:ManualMappingCuration	2022-01-24
EFO:0004276	Stevens-Johnson syndrome	skos:exactMatch	DOID:0050426	Stevens-Johnson syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004277	brain infarction	skos:exactMatch	DOID:3454	brain infarction	semapv:ManualMappingCuration	2022-01-24
EFO:0004278	sudden cardiac arrest	skos:exactMatch	DOID:9007925	Sudden Cardiac Death	semapv:ManualMappingCuration	2023-12-04
EFO:0004280	movement disorder	skos:exactMatch	DOID:480	movement disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004281	testicular neoplasm	skos:exactMatch	DOID:2998	testicular cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0004281	testicular neoplasm	skos:exactMatch	DOID:5557	testicular germ cell cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0004281	testicular neoplasm	skos:exactMatch	DOID:9004207	Testicular Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004282	thoracic aortic aneurysm	skos:exactMatch	DOID:14004	thoracic aortic aneurysm	semapv:ManualMappingCuration	2022-01-24
EFO:0004283	goiter	skos:exactMatch	DOID:12176	goiter	semapv:ManualMappingCuration	2022-01-24
EFO:0004284	upper aerodigestive tract neoplasm	skos:exactMatch	DOID:9006169	Head and Neck Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004285	albuminuria	skos:exactMatch	DOID:9001542	Albuminuria	semapv:ManualMappingCuration	2023-12-04
EFO:0004286	venous thromboembolism	skos:exactMatch	DOID:9003505	Venous Thromboembolism	semapv:ManualMappingCuration	2023-12-04
EFO:0004287	ventricular fibrillation	skos:exactMatch	DOID:9000184	Ventricular Fibrillation	semapv:ManualMappingCuration	2023-12-04
EFO:0004288	colonic neoplasm	skos:exactMatch	DOID:9002928	Colonic Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004289	lymphoid leukemia	skos:exactMatch	DOID:1037	lymphoid leukemia	semapv:ManualMappingCuration	2023-08-20
EFO:0004338	body weight	skos:exactMatch	DOID:9007633	Body Weight	semapv:ManualMappingCuration	2023-12-04
EFO:0004344	birth weight	skos:exactMatch	DOID:9003996	Birth Weight	semapv:ManualMappingCuration	2023-12-04
EFO:0004364	neurobehavioral manifestations	skos:exactMatch	DOID:9002320	Neurobehavioral Manifestations	semapv:ManualMappingCuration	2023-12-04
EFO:0004510	HPV seropositivity	skos:exactMatch	DOID:9003284	HIV Seropositivity	semapv:ManualMappingCuration	2023-12-04
EFO:0004537	neonatal systemic lupus erythematosus	skos:exactMatch	DOID:9007342	Neonatal Systemic Lupus Erythematosus	semapv:ManualMappingCuration	2023-12-04
EFO:0004540	chronic fatigue syndrome	skos:exactMatch	DOID:8544	chronic fatigue syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004562	cryptorchidism	skos:exactMatch	DOID:11383	cryptorchidism	semapv:ManualMappingCuration	2022-01-24
EFO:0004593	gestational diabetes	skos:exactMatch	DOID:11714	gestational diabetes	semapv:ManualMappingCuration	2022-01-24
EFO:0004594	childhood eosinophilic esophagitis	skos:exactMatch	DOID:13922	eosinophilic esophagitis	semapv:ManualMappingCuration	2023-12-04
EFO:0004606	gallbladder neoplasm	skos:exactMatch	DOID:9000011	Gallbladder Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0004607	duodenal ulcer	skos:exactMatch	DOID:1724	duodenal ulcer	semapv:ManualMappingCuration	2022-01-24
EFO:0004608	cystic fibrosis associated meconium ileus	skos:exactMatch	DOID:9006465	Meconium Ileus	semapv:ManualMappingCuration	2023-12-04
EFO:0004610	acute lung injury	skos:exactMatch	DOID:9004610	Acute Lung Injury	semapv:ManualMappingCuration	2023-12-04
EFO:0004616	osteoarthritis, knee	skos:exactMatch	DOID:9002331	Knee Osteoarthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0004683	wet macular degeneration	skos:exactMatch	DOID:10873	Kuhnt-Junius degeneration	semapv:ManualMappingCuration	2022-01-24
EFO:0004686	non-compaction cardiomyopathy	skos:exactMatch	DOID:0060480	left ventricular noncompaction	semapv:ManualMappingCuration	2023-12-04
EFO:0004698	insomnia	skos:exactMatch	DOID:9004576	Sleep Initiation and Maintenance Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0004699	gambling behaviour	skos:exactMatch	DOID:12399	pathological gambling	semapv:ManualMappingCuration	2023-12-04
EFO:0004701	methamphetamine dependence	skos:exactMatch	DOID:670	amphetamine abuse	semapv:ManualMappingCuration	2023-12-04
EFO:0004705	hypothyroidism	skos:exactMatch	DOID:1459	hypothyroidism	semapv:ManualMappingCuration	2022-01-24
EFO:0004707	infantile hypertrophic pyloric stenosis	skos:exactMatch	DOID:12638	hypertrophic pyloric stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004708	nodular sclerosis Hodgkin lymphoma	skos:exactMatch	DOID:8838	Hodgkin's lymphoma, nodular sclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004710	pelvic organ prolapse	skos:exactMatch	DOID:9008409	Pelvic Organ Prolapse	semapv:ManualMappingCuration	2023-12-04
EFO:0004711	elephantiasis	skos:exactMatch	DOID:4976	elephantiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0004712	podoconiosis	skos:exactMatch	DOID:0050138	podoconiosis	semapv:ManualMappingCuration	2022-01-24
EFO:0004714	sexual dysfunction	skos:exactMatch	DOID:1876	sexual dysfunction	semapv:ManualMappingCuration	2022-01-24
EFO:0004715	MRI defined brain infarct	skos:exactMatch	DOID:3454	brain infarction	semapv:ManualMappingCuration	2023-12-04
EFO:0004718	vascular dementia	skos:exactMatch	DOID:8725	vascular dementia	semapv:ManualMappingCuration	2022-01-24
EFO:0004719	pemphigus vulgaris	skos:exactMatch	DOID:0060851	pemphigus vulgaris	semapv:ManualMappingCuration	2022-01-24
EFO:0004720	prion disease	skos:exactMatch	DOID:649	prion disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004723	coronary artery calcification	skos:exactMatch	DOID:9008778	Coronary Artery Calcification	semapv:ManualMappingCuration	2023-12-04
EFO:0004772	early onset hypertension	skos:exactMatch	DOID:9003834	early onset hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0004775	toxic epidermal necrolysis	skos:exactMatch	DOID:0050426	Stevens-Johnson syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0004777	alcohol withdrawal	skos:exactMatch	DOID:0060001	withdrawal disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0004799	cholelithiasis	skos:exactMatch	DOID:10211	cholelithiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0004807	short sleep	skos:exactMatch	DOID:9006913	Short Sleep	semapv:ManualMappingCuration	2023-12-04
EFO:0004826	anti-neutrophil antibody associated vasculitis	skos:exactMatch	DOID:9003819	Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis	semapv:ManualMappingCuration	2023-12-04
EFO:0004859	abdominal aortic artery calcification	skos:exactMatch	DOID:9000815	Aortic Calcification	semapv:ManualMappingCuration	2023-12-04
EFO:0004888	post operative nausea and vomiting	skos:exactMatch	DOID:9003913	Postoperative Nausea and Vomiting	semapv:ManualMappingCuration	2023-12-04
EFO:0004890	anti-social behavior	skos:exactMatch	DOID:10939	antisocial personality disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0004893	testicular dysgenesis syndrome	skos:exactMatch	DOID:9002260	testicular dysgenesis syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0004895	Tourette syndrome	skos:exactMatch	DOID:11119	Gilles de la Tourette syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0004906	lymph node metastatic carcinoma	skos:exactMatch	DOID:9000081	Lymphatic Metastasis	semapv:ManualMappingCuration	2023-12-04
EFO:0004911	familial hypercholesterolemia	skos:exactMatch	DOID:13810	familial hypercholesterolemia	semapv:ManualMappingCuration	2022-01-24
EFO:0004952	disease recurrence	skos:exactMatch	DOID:9002801	Recurrence	semapv:ManualMappingCuration	2023-12-04
EFO:0004986	embryonal carcinoma	skos:exactMatch	DOID:3308	embryonal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0004991	Myasthenia gravis	skos:exactMatch	DOID:437	myasthenia gravis	semapv:ManualMappingCuration	2022-01-24
EFO:0004992	Otitis media	skos:exactMatch	DOID:10754	otitis media	semapv:ManualMappingCuration	2022-01-24
EFO:0004994	lumbar disc degeneration	skos:exactMatch	DOID:90	degenerative disc disease	semapv:ManualMappingCuration	2022-01-24
EFO:0004996	type 1 diabetes nephropathy	skos:exactMatch	DOID:9002165	Diabetic Nephropathies	semapv:ManualMappingCuration	2023-12-04
EFO:0004997	type 2 diabetes nephropathy	skos:exactMatch	DOID:9002165	Diabetic Nephropathies	semapv:ManualMappingCuration	2023-12-04
EFO:0005039	hippocampal atrophy	skos:exactMatch	DOID:9004947	hippocampal atrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0005044	Leishmaniasis	skos:exactMatch	DOID:9065	leishmaniasis	semapv:ManualMappingCuration	2022-01-24
EFO:0005045	visceral Leishmaniasis	skos:exactMatch	DOID:9146	visceral leishmaniasis	semapv:ManualMappingCuration	2022-01-24
EFO:0005046	cutaneous Leishmaniasis	skos:exactMatch	DOID:9111	cutaneous leishmaniasis	semapv:ManualMappingCuration	2022-01-24
EFO:0005088	testicular carcinoma	skos:exactMatch	DOID:2998	testicular cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005135	strain	skos:exactMatch	DOID:9000934	Sprains and Strains	semapv:ManualMappingCuration	2023-12-04
EFO:0005137	conduction system disorder	skos:exactMatch	DOID:10273	heart conduction disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005138	acquired long QT syndrome	skos:exactMatch	DOID:2843	long QT syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0005140	autoimmune disease	skos:exactMatch	DOID:417	autoimmune disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005203	eating disorder	skos:exactMatch	DOID:8670	eating disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005204	bulimia nervosa	skos:exactMatch	DOID:12129	bulimia nervosa	semapv:ManualMappingCuration	2022-01-24
EFO:0005207	congenital heart disease	skos:exactMatch	DOID:1682	congenital heart disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005220	pulmonary neuroendocrine tumor	skos:exactMatch	DOID:5410	pulmonary neuroendocrine tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0005221	cholangiocarcinoma	skos:exactMatch	DOID:4947	cholangiocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005222	avian influenza	skos:exactMatch	DOID:4492	avian influenza	semapv:ManualMappingCuration	2022-01-24
EFO:0005223	acute stress reaction	skos:exactMatch	DOID:6088	acute stress disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005224	Q fever	skos:exactMatch	DOID:11100	Q fever	semapv:ManualMappingCuration	2022-01-24
EFO:0005225	human african trypanosomiasis	skos:exactMatch	DOID:10112	sleeping sickness	semapv:ManualMappingCuration	2022-01-24
EFO:0005226	swine influenza	skos:exactMatch	DOID:0050211	swine influenza	semapv:ManualMappingCuration	2022-01-24
EFO:0005230	anxiety	skos:exactMatch	DOID:2030	anxiety disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0005232	endometrium adenocarcinoma	skos:exactMatch	DOID:2870	endometrial adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005235	primitive neuroectodermal tumor	skos:exactMatch	DOID:171	neuroectodermal tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0005239	aortic valve calcification	skos:exactMatch	DOID:9004397	Calcification of Aortic Valve	semapv:ManualMappingCuration	2023-12-04
EFO:0005240	rhegmatogenous retinal detachment	skos:exactMatch	DOID:9007109	Rhegmatogenous Retinal Detachment, Autosomal Dominant	semapv:ManualMappingCuration	2023-12-04
EFO:0005242	methamphetamine-induced psychosis	skos:exactMatch	DOID:1742	drug psychosis	semapv:ManualMappingCuration	2023-12-04
EFO:0005246	hypersomnia	skos:exactMatch	DOID:8619	recurrent hypersomnia	semapv:ManualMappingCuration	2023-12-04
EFO:0005250	occupation-related stress disorder	skos:exactMatch	DOID:9004763	Trauma and Stressor Related Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0005251	hypotension	skos:exactMatch	DOID:9006024	Hypotension	semapv:ManualMappingCuration	2023-12-04
EFO:0005252	orthostatic hypotension	skos:exactMatch	DOID:9005950	Orthostatic Hypotension	semapv:ManualMappingCuration	2023-12-04
EFO:0005254	neurally mediated hypotension	skos:exactMatch	DOID:9006024	Hypotension	semapv:ManualMappingCuration	2023-12-04
EFO:0005262	mitral annular calcification	skos:exactMatch	DOID:9002259	mitral annular calcification	semapv:ManualMappingCuration	2023-12-04
EFO:0005269	congenital heart malformation	skos:exactMatch	DOID:1682	congenital heart disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005279	temporomandibular joint disorder	skos:exactMatch	DOID:9006281	Temporomandibular Joint Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0005287	reticulum cell sarcoma	skos:exactMatch	DOID:8538	reticulosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005288	non-small cell lung adenocarcinoma	skos:exactMatch	DOID:3910	lung adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005297	Granulomatosis with Polyangiitis	skos:exactMatch	DOID:12132	granulomatosis with polyangiitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005303	sudden infant death syndrome	skos:exactMatch	DOID:9007	sudden infant death syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0005304	atrial conduction disease	skos:exactMatch	DOID:9001836	Cardiac Conduction Defect	semapv:ManualMappingCuration	2023-12-04
EFO:0005305	atrioventricular node disease	skos:exactMatch	DOID:0050820	atrioventricular block	semapv:ManualMappingCuration	2023-12-04
EFO:0005306	ventricular tachycardia	skos:exactMatch	DOID:9005141	Ventricular Tachycardia	semapv:ManualMappingCuration	2023-12-04
EFO:0005307	torsades de pointes	skos:exactMatch	DOID:9005444	Torsades de Pointes	semapv:ManualMappingCuration	2023-12-04
EFO:0005308	atrial tachycardia	skos:exactMatch	DOID:9003484	Atrial Tachycardia	semapv:ManualMappingCuration	2023-12-04
EFO:0005319	contact dermatitis	skos:exactMatch	DOID:2773	contact dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005320	contact dermatitis due to nickel	skos:exactMatch	DOID:0040046	nickel allergic contact dermatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0005321	molar-incisor hypomineralization	skos:exactMatch	DOID:693	dental enamel hypoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0005400	chemotherapy-induced alopecia	skos:exactMatch	DOID:9002102	chemotherapy-induced alopecia	semapv:ManualMappingCuration	2023-12-04
EFO:0005406	colorectal adenoma	skos:exactMatch	DOID:0050860	colorectal adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005406	colorectal adenoma	skos:exactMatch	DOID:0050914	large intestine adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005407	psychosis	skos:exactMatch	DOID:2468	psychotic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005410	tooth agenesis	skos:exactMatch	DOID:0050591	tooth agenesis	semapv:ManualMappingCuration	2022-01-24
EFO:0005411	schizoaffective disorder	skos:exactMatch	DOID:5418	schizoaffective disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005414	airway hyperresponsiveness	skos:exactMatch	DOID:2841	asthma	semapv:ManualMappingCuration	2023-12-04
EFO:0005423	adolescent idiopathic scoliosis	skos:exactMatch	DOID:0060250	idiopathic scoliosis	semapv:ManualMappingCuration	2023-12-04
EFO:0005424	dyslexia	skos:exactMatch	DOID:4428	dyslexia	semapv:ManualMappingCuration	2022-01-24
EFO:0005425	language impairment	skos:exactMatch	DOID:93	language disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005429	borderline personality disorder symptom	skos:exactMatch	DOID:10930	borderline personality disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0005524	large artery stroke	skos:exactMatch	DOID:9006885	large artery stroke	semapv:ManualMappingCuration	2023-12-04
EFO:0005529	Chagas cardiomyopathy	skos:exactMatch	DOID:9004422	Chagas Cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0005531	urticaria	skos:exactMatch	DOID:1555	urticaria	semapv:ManualMappingCuration	2022-01-24
EFO:0005532	angioedema	skos:exactMatch	DOID:1558	angioedema	semapv:ManualMappingCuration	2022-01-24
EFO:0005534	delayed encephalopathy after acute carbon monoxide poisoning	skos:exactMatch	DOID:936	brain disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005537	triple-negative breast cancer	skos:exactMatch	DOID:0060081	triple-receptor negative breast cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005539	adrenal gland disease	skos:exactMatch	DOID:9553	adrenal gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005540	bile duct carcinoma	skos:exactMatch	DOID:4897	bile duct carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005541	bone development disease	skos:exactMatch	DOID:0080006	bone development disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005542	botulism	skos:exactMatch	DOID:11976	botulism	semapv:ManualMappingCuration	2022-01-24
EFO:0005543	glioma	skos:exactMatch	DOID:3070	high grade glioma	semapv:ManualMappingCuration	2023-12-04
EFO:0005545	congenital disorder of glycosylation type I	skos:exactMatch	DOID:0050570	congenital disorder of glycosylation type I	semapv:ManualMappingCuration	2022-01-24
EFO:0005546	congenital disorder of glycosylation type II	skos:exactMatch	DOID:0050571	congenital disorder of glycosylation type II	semapv:ManualMappingCuration	2022-01-24
EFO:0005547	dengue disease	skos:exactMatch	DOID:12205	dengue disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005548	developmental disorder of mental health	skos:exactMatch	DOID:0060037	developmental disorder of mental health	semapv:ManualMappingCuration	2022-01-24
EFO:0005549	diphtheria	skos:exactMatch	DOID:11405	diphtheria	semapv:ManualMappingCuration	2022-01-24
EFO:0005551	dysembryoplastic neuroepithelial tumor	skos:exactMatch	DOID:2679	dysembryoplastic neuroepithelial tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0005553	eccrine sweat gland cancer	skos:exactMatch	DOID:4921	eccrine sweat gland cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005555	gamma chain deficiency	skos:exactMatch	DOID:0060013	X-linked severe combined immunodeficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0005556	Gilbert syndrome	skos:exactMatch	DOID:2739	Gilbert syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0005557	gum cancer	skos:exactMatch	DOID:8602	gum cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005558	hemolytic anemia	skos:exactMatch	DOID:583	hemolytic anemia	semapv:ManualMappingCuration	2022-01-24
EFO:0005560	hereditary multiple exostoses	skos:exactMatch	DOID:206	hereditary multiple exostoses	semapv:ManualMappingCuration	2022-01-24
EFO:0005561	histiocytoma	skos:exactMatch	DOID:4231	histiocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005562	hydronephrosis	skos:exactMatch	DOID:11111	hydronephrosis	semapv:ManualMappingCuration	2022-01-24
EFO:0005565	janus kinase-3 deficiency	skos:exactMatch	DOID:0060008	janus kinase-3 deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0005567	malignant peritoneal mesothelioma	skos:exactMatch	DOID:1788	peritoneal mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:0005568	methylmalonic aciduria and homocystinuria type cblE	skos:exactMatch	DOID:0050732	methylmalonic aciduria and homocystinuria type cblE	semapv:ManualMappingCuration	2022-01-24
EFO:0005569	microphthalmia	skos:exactMatch	DOID:10629	microphthalmia	semapv:ManualMappingCuration	2022-01-24
EFO:0005570	oral cavity cancer	skos:exactMatch	DOID:8618	oral cavity cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005571	osteochondrodysplasia	skos:exactMatch	DOID:2256	osteochondrodysplasia	semapv:ManualMappingCuration	2022-01-24
EFO:0005576	pernicious anemia	skos:exactMatch	DOID:13381	pernicious anemia	semapv:ManualMappingCuration	2022-01-24
EFO:0005577	pharynx cancer	skos:exactMatch	DOID:0060119	pharynx cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005578	pituitary cancer	skos:exactMatch	DOID:1785	pituitary cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005579	pseudohermaphroditism	skos:exactMatch	DOID:3765	pseudohermaphroditism	semapv:ManualMappingCuration	2022-01-24
EFO:0005580	red color blindness	skos:exactMatch	DOID:13910	red color blindness	semapv:ManualMappingCuration	2022-01-24
EFO:0005581	red-green color blindness	skos:exactMatch	DOID:13909	red-green color blindness	semapv:ManualMappingCuration	2022-01-24
EFO:0005582	renal pelvis carcinoma	skos:exactMatch	DOID:4919	renal pelvis carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005583	rickets	skos:exactMatch	DOID:10609	rickets	semapv:ManualMappingCuration	2022-01-24
EFO:0005584	seborrheic keratosis	skos:exactMatch	DOID:6498	seborrheic keratosis	semapv:ManualMappingCuration	2022-01-24
EFO:0005585	shigellosis	skos:exactMatch	DOID:12385	shigellosis	semapv:ManualMappingCuration	2022-01-24
EFO:0005588	small intestine carcinoma	skos:exactMatch	DOID:4907	small intestine carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005590	steroid inherited metabolic disorder	skos:exactMatch	DOID:1701	steroid inherited metabolic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005591	sweat gland carcinoma	skos:exactMatch	DOID:5667	sweat gland carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005592	T-cell leukemia	skos:exactMatch	DOID:5603	T-cell acute lymphoblastic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:0005592	T-cell leukemia	skos:exactMatch	DOID:715	T-cell lymphoblastic leukemia/lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005593	tetanus	skos:exactMatch	DOID:11338	tetanus	semapv:ManualMappingCuration	2022-01-24
EFO:0005595	toxic encephalopathy	skos:exactMatch	DOID:3602	toxic encephalopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0005596	vitamin metabolic disorder	skos:exactMatch	DOID:0050718	vitamin metabolic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005597	methylmalonic aciduria and homocystinuria type cblG	skos:exactMatch	DOID:0050733	methylmalonic aciduria and homocystinuria type cblG	semapv:ManualMappingCuration	2022-01-24
EFO:0005611	opioid dependence	skos:exactMatch	DOID:2559	opiate dependence	semapv:ManualMappingCuration	2022-01-24
EFO:0005612	morphine dependence	skos:exactMatch	DOID:2560	morphine dependence	semapv:ManualMappingCuration	2022-01-24
EFO:0005622	Crohn's colitis	skos:exactMatch	DOID:0060192	Crohn's colitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005623	distal colitis	skos:exactMatch	DOID:8577	ulcerative colitis	semapv:ManualMappingCuration	2023-12-04
EFO:0005624	ileocolitis	skos:exactMatch	DOID:0060190	ileocolitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005625	oral Crohn's disease	skos:exactMatch	DOID:8778	Crohn's disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005626	pancolitis	skos:exactMatch	DOID:9001672	pancolitis	semapv:ManualMappingCuration	2023-12-04
EFO:0005627	perianal Crohn's disease	skos:exactMatch	DOID:9004680	perianal Crohn's disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005628	proctitis	skos:exactMatch	DOID:3127	proctitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005631	rectal adenocarcinoma	skos:exactMatch	DOID:1996	rectum adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005649	spondylolysis	skos:exactMatch	DOID:2300	spondylolysis	semapv:ManualMappingCuration	2022-01-24
EFO:0005669	intracerebral hemorrhage	skos:exactMatch	DOID:9002676	Cerebral Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0005672	acute coronary syndrome	skos:exactMatch	DOID:9001686	Acute Coronary Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0005676	Autoimmune Hepatitis	skos:exactMatch	DOID:2048	autoimmune hepatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005681	Staphylococcus aureus infection	skos:exactMatch	DOID:9008885	Staphylococcal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0005687	fibromyalgia	skos:exactMatch	DOID:631	fibromyalgia	semapv:ManualMappingCuration	2022-01-24
EFO:0005701	malignant rhabdoid tumour	skos:exactMatch	DOID:3672	rhabdoid cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005708	renal cell adenocarcinoma	skos:exactMatch	DOID:4450	renal cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0005716	retinal cancer	skos:exactMatch	DOID:4645	retinal cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005717	retinoblastoma (nonhereditary)	skos:exactMatch	DOID:768	retinoblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:0005741	infectious disease	skos:exactMatch	DOID:0050117	disease by infectious agent	semapv:ManualMappingCuration	2022-01-24
EFO:0005751	eye allergy	skos:exactMatch	DOID:1205	allergic disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005753	ocular vascular disease	skos:exactMatch	DOID:178	vascular disease	semapv:ManualMappingCuration	2023-12-04
EFO:0005754	parathyroid disease	skos:exactMatch	DOID:11201	parathyroid gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005755	rheumatic disease	skos:exactMatch	DOID:1575	rheumatic disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005757	vaginal inflammation	skos:exactMatch	DOID:2170	vaginitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005758	cycloplegia	skos:exactMatch	DOID:10033	cycloplegia	semapv:ManualMappingCuration	2022-01-24
EFO:0005761	lupus nephritis	skos:exactMatch	DOID:0080162	lupus nephritis	semapv:ManualMappingCuration	2022-01-24
EFO:0005762	neuropathic pain	skos:exactMatch	DOID:9005968	Neuralgia	semapv:ManualMappingCuration	2023-12-04
EFO:0005769	calcium metabolic disease	skos:exactMatch	DOID:10575	calcium metabolism disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005771	ovarian disease	skos:exactMatch	DOID:1100	ovarian disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005772	neurodegenerative disease	skos:exactMatch	DOID:1289	neurodegenerative disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005773	retinal detachment	skos:exactMatch	DOID:5327	retinal detachment	semapv:ManualMappingCuration	2022-01-24
EFO:0005774	brain disease	skos:exactMatch	DOID:936	brain disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005775	aortic disease	skos:exactMatch	DOID:520	aortic disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005782	age-related hearing impairment	skos:exactMatch	DOID:9000307	Presbycusis	semapv:ManualMappingCuration	2023-12-04
EFO:0005783	NUT midline carcinoma	skos:exactMatch	DOID:0060463	NUT midline carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005784	embryonal neoplasm	skos:exactMatch	DOID:688	embryonal cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0005785	blastoma	skos:exactMatch	DOID:0070003	blastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005785	blastoma	skos:exactMatch	DOID:4766	embryoma	semapv:ManualMappingCuration	2022-07-21
EFO:0005799	neonatal abstinence syndrome	skos:exactMatch	DOID:9828	neonatal abstinence syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0005800	substance withdrawal syndrome	skos:exactMatch	DOID:0060001	withdrawal disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0005801	cholesterol embolism	skos:exactMatch	DOID:1461	cholesterol embolism	semapv:ManualMappingCuration	2022-01-24
EFO:0005802	cartilage disease	skos:exactMatch	DOID:1222	cartilage disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005803	hematologic disease	skos:exactMatch	DOID:74	hematopoietic system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005804	polycythemia	skos:exactMatch	DOID:8432	polycythemia	semapv:ManualMappingCuration	2022-01-24
EFO:0005805	polycythemia due to hypoxia	skos:exactMatch	DOID:2835	polycythemia due to hypoxia	semapv:ManualMappingCuration	2022-01-24
EFO:0005809	type II hypersensitivity reaction disease	skos:exactMatch	DOID:417	autoimmune disease	semapv:ManualMappingCuration	2022-01-24
EFO:0005815	tauopathy	skos:exactMatch	DOID:680	tauopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0005840	Pyruvate kinase hyperactivity	skos:exactMatch	DOID:9002812	Elevated Adenosine Triphosphate of Erythrocytes	semapv:ManualMappingCuration	2023-12-04
EFO:0005846	cryoglobulinemia	skos:exactMatch	DOID:2917	cryoglobulinemia	semapv:ManualMappingCuration	2022-01-24
EFO:0005854	allergic rhinitis	skos:exactMatch	DOID:4481	allergic rhinitis	semapv:ManualMappingCuration	2022-01-24
EFO:0005855	narcolepsy without cataplexy	skos:exactMatch	DOID:8986	narcolepsy	semapv:ManualMappingCuration	2023-12-04
EFO:0005856	arthritis	skos:exactMatch	DOID:848	arthritis	semapv:ManualMappingCuration	2022-01-24
EFO:0005878	vitamin deficiency	skos:exactMatch	DOID:9004644	Avitaminosis	semapv:ManualMappingCuration	2023-12-04
EFO:0005895	ossification of the posterior longitudinal ligament of the spine	skos:exactMatch	DOID:0060887	ossification of the posterior longitudinal ligament of spine	semapv:ManualMappingCuration	2022-01-24
EFO:0005917	generalised epilepsy	skos:exactMatch	DOID:1827	idiopathic generalized epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:0005917	generalised epilepsy	skos:exactMatch	DOID:9001793	Generalized Epilepsy	semapv:ManualMappingCuration	2023-12-04
EFO:0005922	esophageal squamous cell carcinoma	skos:exactMatch	DOID:3748	esophagus squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0005923	AVL induced bursal lymphoma	skos:exactMatch	DOID:9006219	Avian Leukosis	semapv:ManualMappingCuration	2023-12-04
EFO:0005924	binge eating	skos:exactMatch	DOID:9004099	Bulimia	semapv:ManualMappingCuration	2023-12-04
EFO:0005932	animal disease	skos:exactMatch	DOID:9004985	Animal Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0005940	psychotic symptoms	skos:exactMatch	DOID:2468	psychotic disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0005950	head and neck neoplasia	skos:exactMatch	DOID:9006169	Head and Neck Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0005952	non-Hodgkins lymphoma	skos:exactMatch	DOID:0060060	non-Hodgkin lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006313	chemotherapy-induced oral mucositis	skos:exactMatch	DOID:9005893	chemotherapy-induced oral mucositis	semapv:ManualMappingCuration	2023-12-04
EFO:0006315	thiopurine immunosuppressant-induced pancreatitis	skos:exactMatch	DOID:4989	pancreatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0006318	breast ductal adenocarcinoma	skos:exactMatch	DOID:3007	breast ductal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006321	antidepressant-induced dizziness	skos:exactMatch	DOID:9006810	Drug-Related Side Effects and Adverse Reactions	semapv:ManualMappingCuration	2023-12-04
EFO:0006322	antidepressant-induced sexual dysfunction	skos:exactMatch	DOID:1876	sexual dysfunction	semapv:ManualMappingCuration	2023-12-04
EFO:0006323	antidepressant-induced visual impairment	skos:exactMatch	DOID:1432	blindness	semapv:ManualMappingCuration	2023-12-04
EFO:0006324	antidepressant-induced hearing impairment	skos:exactMatch	DOID:0070310	drug-induced hearing loss	semapv:ManualMappingCuration	2023-12-04
EFO:0006338	pit and fissure surface dental caries	skos:exactMatch	DOID:216	dental caries	semapv:ManualMappingCuration	2023-12-04
EFO:0006339	smooth surface dental caries	skos:exactMatch	DOID:216	dental caries	semapv:ManualMappingCuration	2023-12-04
EFO:0006342	aggressive periodontitis	skos:exactMatch	DOID:1474	aggressive periodontitis	semapv:ManualMappingCuration	2022-01-24
EFO:0006343	chronic periodontitis	skos:exactMatch	DOID:9001004	Chronic Periodontitis	semapv:ManualMappingCuration	2023-12-04
EFO:0006346	severe cutaneous adverse reaction	skos:exactMatch	DOID:9004739	Cicatrix	semapv:ManualMappingCuration	2023-12-04
EFO:0006352	laryngeal squamous cell carcinoma	skos:exactMatch	DOID:2876	laryngeal squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006387	cystadenocarcinoma	skos:exactMatch	DOID:3111	cystadenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006388	cystic renal cell carcinoma	skos:exactMatch	DOID:9002228	cystic renal cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0006391	dopaminergic neuroblastoma	skos:exactMatch	DOID:9005544	dopaminergic neuroblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:0006452	malignant epithelioid mesothelioma	skos:exactMatch	DOID:4489	malignant epithelial mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:0006460	ovarian adenocarcinoma	skos:exactMatch	DOID:3713	ovary adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006461	ovarian granulosa tumour	skos:exactMatch	DOID:9002210	Granulosa Cell Tumor of the Ovary	semapv:ManualMappingCuration	2023-12-04
EFO:0006462	ovarian mucinous adenocarcinoma	skos:exactMatch	DOID:3606	ovarian mucinous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006463	ovarian teratoma	skos:exactMatch	DOID:5567	ovarian germ cell teratoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006471	pancreatic tubular adenocarcinoma	skos:exactMatch	DOID:3498	pancreatic ductal adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0006475	plasma cell leukemia	skos:exactMatch	DOID:9513	plasma cell leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0006497	transitional cell papilloma	skos:exactMatch	DOID:2670	transitional papilloma	semapv:ManualMappingCuration	2022-01-24
EFO:0006500	tubular adenocarcinoma	skos:exactMatch	DOID:4929	tubular adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006505	chronic bronchitis	skos:exactMatch	DOID:9007651	Chronic Bronchitis	semapv:ManualMappingCuration	2023-12-04
EFO:0006509	Varicella Zoster infection	skos:exactMatch	DOID:9004668	Varicella Zoster infection	semapv:ManualMappingCuration	2023-12-04
EFO:0006510	Herpes Zoster	skos:exactMatch	DOID:8536	herpes zoster	semapv:ManualMappingCuration	2022-01-24
EFO:0006511	Kashin-Beck disease	skos:exactMatch	DOID:9004038	Kashin-Beck Disease	semapv:ManualMappingCuration	2023-12-04
EFO:0006513	hereditary hemochromatosis type 1	skos:exactMatch	DOID:0111029	hemochromatosis type 1	semapv:ManualMappingCuration	2022-01-24
EFO:0006519	MMR-related febrile seizures	skos:exactMatch	DOID:9007956	Febrile Seizures	semapv:ManualMappingCuration	2023-12-04
EFO:0006544	bladder transitional cell carcinoma	skos:exactMatch	DOID:4006	bladder urothelial carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006545	brain glioblastoma	skos:exactMatch	DOID:3073	brain glioblastoma multiforme	semapv:ManualMappingCuration	2022-01-24
EFO:0006718	ovarian leiomyosarcoma	skos:exactMatch	DOID:5263	ovary leiomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006719	mesonephric adenocarcinoma	skos:exactMatch	DOID:4468	clear cell adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0006732	pancreatic adenosquamous carcinoma	skos:exactMatch	DOID:5637	pancreatic adenosquamous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006738	plasmacytoma	skos:exactMatch	DOID:3721	plasmacytoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006740	pulmonary mucoepidermoid carcinoma	skos:exactMatch	DOID:0050932	lung mucoepidermoid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0006772	undifferentiated carcinoma	skos:exactMatch	DOID:305	carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0006788	anxiety disorder	skos:exactMatch	DOID:2030	anxiety disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0006789	typhoid fever	skos:exactMatch	DOID:13258	typhoid fever	semapv:ManualMappingCuration	2022-01-24
EFO:0006790	cerebral amyloid angiopathy	skos:exactMatch	DOID:9246	cerebral amyloid angiopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0006791	vascular brain injury	skos:exactMatch	DOID:9001829	Cerebrovascular Trauma	semapv:ManualMappingCuration	2023-12-04
EFO:0006792	Lewy body dementia	skos:exactMatch	DOID:12217	Lewy body dementia	semapv:ManualMappingCuration	2022-01-24
EFO:0006803	vasculitis	skos:exactMatch	DOID:865	vasculitis	semapv:ManualMappingCuration	2022-01-24
EFO:0006812	autoimmune thyroid disease	skos:exactMatch	DOID:7188	autoimmune thyroiditis	semapv:ManualMappingCuration	2022-01-24
EFO:0006813	atrophic thyroiditis	skos:exactMatch	DOID:7188	autoimmune thyroiditis	semapv:ManualMappingCuration	2023-12-04
EFO:0006817	yang deficiency	skos:exactMatch	DOID:9003352	Yang Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0006818	stricture	skos:exactMatch	DOID:9001627	Pathologic Constriction	semapv:ManualMappingCuration	2023-12-04
EFO:0006834	septic shock	skos:exactMatch	DOID:9007601	endotoxin shock	semapv:ManualMappingCuration	2023-12-04
EFO:0006835	pyoderma gangrenosum	skos:exactMatch	DOID:8553	pyoderma gangrenosum	semapv:ManualMappingCuration	2022-01-24
EFO:0006856	leucine-induced hypoglycemia	skos:exactMatch	DOID:0112262	leucine-sensitive hypoglycemia of infancy	semapv:ManualMappingCuration	2023-12-04
EFO:0006857	cerebral malaria	skos:exactMatch	DOID:14069	cerebral malaria	semapv:ManualMappingCuration	2022-01-24
EFO:0006858	epithelial neoplasm	skos:exactMatch	DOID:9006493	Glandular and Epithelial Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0006859	head and neck malignant neoplasia	skos:exactMatch	DOID:11934	head and neck cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0006861	male breast carcinoma	skos:exactMatch	DOID:1614	male breast cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0006861	male breast carcinoma	skos:exactMatch	DOID:9003042	male breast carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0006862	Meniere disease	skos:exactMatch	DOID:9849	Meniere's disease	semapv:ManualMappingCuration	2022-01-24
EFO:0006865	urgency urinary incontinence	skos:exactMatch	DOID:9007300	Urinary Incontinence, Urge	semapv:ManualMappingCuration	2023-12-04
EFO:0006884	mouth mucous membrane leukoplakia	skos:exactMatch	DOID:9655	oral mucosa leukoplakia	semapv:ManualMappingCuration	2023-12-04
EFO:0006885	leukoplakia of tongue	skos:exactMatch	DOID:9655	oral mucosa leukoplakia	semapv:ManualMappingCuration	2023-12-04
EFO:0006888	vascular malformation	skos:exactMatch	DOID:9003191	Vascular Malformations	semapv:ManualMappingCuration	2023-12-04
EFO:0006889	monoclonal B-cell lymphocytosis	skos:exactMatch	DOID:9006737	Monoclonal B-Cell Lymphocytosis	semapv:ManualMappingCuration	2023-12-04
EFO:0006890	fibrosis	skos:exactMatch	DOID:9000784	Fibrosis	semapv:ManualMappingCuration	2023-12-04
EFO:0006891	breast adenosis	skos:exactMatch	DOID:5998	microglandular adenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0006892	cutaneous precancerous condition	skos:exactMatch	DOID:0060071	pre-malignant neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:0006911	Chemotherapy-induced nausea and vomiting	skos:exactMatch	DOID:9005182	Chemotherapy-induced nausea and vomiting	semapv:ManualMappingCuration	2023-12-04
EFO:0006912	Radiation-induced nausea and vomiting	skos:exactMatch	DOID:9000111	Radiation Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0006917	spontaneous preterm birth	skos:exactMatch	DOID:9003507	Premature Birth	semapv:ManualMappingCuration	2023-12-04
EFO:0006926	acquired aplastic anemia	skos:exactMatch	DOID:12449	aplastic anemia	semapv:ManualMappingCuration	2023-12-04
EFO:0006927	severe aplastic anemia	skos:exactMatch	DOID:12449	aplastic anemia	semapv:ManualMappingCuration	2023-12-04
EFO:0006928	motion sickness	skos:exactMatch	DOID:2951	motion sickness	semapv:ManualMappingCuration	2023-12-04
EFO:0006951	ototoxicity	skos:exactMatch	DOID:0070310	drug-induced hearing loss	semapv:ManualMappingCuration	2023-12-04
EFO:0007051	vein graft stenosis	skos:exactMatch	DOID:9003230	Graft Occlusion, Vascular	semapv:ManualMappingCuration	2023-12-04
EFO:0007066	chronic ulcer of skin	skos:exactMatch	DOID:8549	chronic ulcer of skin	semapv:ManualMappingCuration	2022-01-24
EFO:0007067	decubitus ulcer	skos:exactMatch	DOID:8717	decubitus ulcer	semapv:ManualMappingCuration	2022-01-24
EFO:0007068	ulcer of lower limb	skos:exactMatch	DOID:8529	ulcer of lower limbs	semapv:ManualMappingCuration	2022-01-24
EFO:0007126	Acanthamoeba keratitis	skos:exactMatch	DOID:9001552	Acanthamoeba Keratitis	semapv:ManualMappingCuration	2023-12-04
EFO:0007127	actinobacillosis	skos:exactMatch	DOID:4974	actinobacillosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007128	actinomycosis	skos:exactMatch	DOID:8478	actinomycosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007129	acute chest syndrome	skos:exactMatch	DOID:1584	acute chest syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007130	acute disseminated encephalomyelitis	skos:exactMatch	DOID:639	acute disseminated encephalomyelitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007131	acute hemorrhagic conjunctivitis	skos:exactMatch	DOID:11227	acute hemorrhagic conjunctivitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007132	acute hemorrhagic leukoencephalitis	skos:exactMatch	DOID:10992	acute hemorrhagic leukoencephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007133	adenomyoma	skos:exactMatch	DOID:2609	adenomyoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007134	adenosarcoma	skos:exactMatch	DOID:1974	adenosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007135	adult-onset Still's disease	skos:exactMatch	DOID:14256	adult-onset Still's disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007136	agnosia	skos:exactMatch	DOID:4090	agnosia	semapv:ManualMappingCuration	2022-01-24
EFO:0007137	AIDS related complex	skos:exactMatch	DOID:9003393	AIDS-Related Complex	semapv:ManualMappingCuration	2023-12-04
EFO:0007138	akinetic mutism	skos:exactMatch	DOID:4267	akinetic mutism	semapv:ManualMappingCuration	2022-01-24
EFO:0007139	aleutian mink disease	skos:exactMatch	DOID:2934	aleutian mink disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007140	allergic bronchopulmonary aspergillosis	skos:exactMatch	DOID:13166	allergic bronchopulmonary aspergillosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007141	allergic conjunctivitis	skos:exactMatch	DOID:11204	allergic conjunctivitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007142	Alphavirus infectious disease	skos:exactMatch	DOID:9007339	Alphavirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007143	alveolar soft part sarcoma	skos:exactMatch	DOID:4239	alveolar soft part sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007144	amebiasis	skos:exactMatch	DOID:9181	amebiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007145	ancylostomiasis	skos:exactMatch	DOID:12841	ancylostomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007146	anisakiasis	skos:exactMatch	DOID:7033	anisakiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007147	anogenital venereal wart	skos:exactMatch	DOID:11168	anogenital venereal wart	semapv:ManualMappingCuration	2022-01-24
EFO:0007148	aortic valve insufficiency	skos:exactMatch	DOID:57	aortic valve insufficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0007149	appendicitis	skos:exactMatch	DOID:8337	appendicitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007150	Arenaviridae infectious disease	skos:exactMatch	DOID:3944	Arenaviridae infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007151	Arenavirus hemorrhagic fever	skos:exactMatch	DOID:9006665	Arenavirus hemorrhagic fever	semapv:ManualMappingCuration	2023-12-04
EFO:0007152	Arterivirus infectious disease	skos:exactMatch	DOID:9001975	Arterivirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007153	asbestosis	skos:exactMatch	DOID:10320	asbestosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007154	ascariasis	skos:exactMatch	DOID:456	ascariasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007155	ascaridiasis	skos:exactMatch	DOID:3108	ascaridiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007156	Ascaridida infectious disease	skos:exactMatch	DOID:9000395	Ascaridida Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007157	aspergillosis	skos:exactMatch	DOID:13564	aspergillosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007158	Astroviridae infectious disease	skos:exactMatch	DOID:9002845	Astroviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007159	atrophic rhinitis	skos:exactMatch	DOID:4731	atrophic rhinitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007160	autoimmune thrombocytopenic purpura	skos:exactMatch	DOID:8924	autoimmune thrombocytopenic purpura	semapv:ManualMappingCuration	2022-01-24
EFO:0007161	Avulavirus infectious disease	skos:exactMatch	DOID:9002653	Avulavirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007162	babesiosis	skos:exactMatch	DOID:9643	babesiosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007163	balantidiasis	skos:exactMatch	DOID:12386	balantidiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007164	Balkan nephropathy	skos:exactMatch	DOID:3052	Balkan nephropathy	semapv:ManualMappingCuration	2022-01-24
EFO:0007165	Barre-Lieou syndrome	skos:exactMatch	DOID:6692	Barre-Lieou syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007166	bartonellosis	skos:exactMatch	DOID:11102	bartonellosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007167	Bell's palsy	skos:exactMatch	DOID:12506	Bell's palsy	semapv:ManualMappingCuration	2022-01-24
EFO:0007168	berylliosis	skos:exactMatch	DOID:10322	berylliosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007169	biliary dyskinesia	skos:exactMatch	DOID:4140	biliary dyskinesia	semapv:ManualMappingCuration	2022-01-24
EFO:0007170	bird fancier's lung	skos:exactMatch	DOID:13891	bird fancier's lung	semapv:ManualMappingCuration	2022-01-24
EFO:0007171	black piedra	skos:exactMatch	DOID:12711	black piedra	semapv:ManualMappingCuration	2022-01-24
EFO:0007172	blackwater fever	skos:exactMatch	DOID:14068	blackwater fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007173	Blastocystis hominis infectious disease	skos:exactMatch	DOID:9008966	Blastocystis Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007174	blastomycosis	skos:exactMatch	DOID:12663	blastomycosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007175	blind loop syndrome	skos:exactMatch	DOID:10606	blind loop syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007176	bone giant cell tumor	skos:exactMatch	DOID:4305	bone giant cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0007177	border disease	skos:exactMatch	DOID:9005625	Border Disease	semapv:ManualMappingCuration	2023-12-04
EFO:0007178	borna disease	skos:exactMatch	DOID:5154	borna disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007179	boutonneuse fever	skos:exactMatch	DOID:14095	boutonneuse fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007180	bovine respiratory disease complex	skos:exactMatch	DOID:9006345	Bovine Respiratory Disease Complex	semapv:ManualMappingCuration	2023-12-04
EFO:0007181	bovine virus diarrhea-mucosal disease	skos:exactMatch	DOID:9008210	Bovine Virus Diarrhea-Mucosal Disease	semapv:ManualMappingCuration	2023-12-04
EFO:0007182	Brill-Zinsser disease	skos:exactMatch	DOID:11254	Brill-Zinsser disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007183	bronchiolitis obliterans	skos:exactMatch	DOID:2799	bronchiolitis obliterans	semapv:ManualMappingCuration	2022-01-24
EFO:0007184	bronchopneumonia	skos:exactMatch	DOID:12375	bronchopneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:0007185	brucellosis	skos:exactMatch	DOID:11077	brucellosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007186	bulbar polio	skos:exactMatch	DOID:9786	bulbar polio	semapv:ManualMappingCuration	2022-01-24
EFO:0007187	bullous pemphigoid	skos:exactMatch	DOID:8506	bullous pemphigoid	semapv:ManualMappingCuration	2022-01-24
EFO:0007188	Bunyaviridae infectious disease	skos:exactMatch	DOID:9004137	Bunyaviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007189	Caliciviridae infectious disease	skos:exactMatch	DOID:9006923	Caliciviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007190	campylobacteriosis	skos:exactMatch	DOID:13622	campylobacteriosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007191	cannabis dependence	skos:exactMatch	DOID:1849	cannabis dependence	semapv:ManualMappingCuration	2022-01-24
EFO:0007191	cannabis dependence	skos:exactMatch	DOID:9505	cannabis abuse	semapv:ManualMappingCuration	2022-01-24
EFO:0007192	Caplan's syndrome	skos:exactMatch	DOID:10326	Caplan's syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007193	carbamoyl phosphate synthetase I deficiency disease	skos:exactMatch	DOID:9280	carbamoyl phosphate synthetase I deficiency disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007194	Cardiovirus infectious disease	skos:exactMatch	DOID:9004531	Cardiovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007195	cat-scratch disease	skos:exactMatch	DOID:11258	cat-scratch disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007196	Cauda equina syndrome	skos:exactMatch	DOID:11577	Cauda equina syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007197	cecal benign neoplasm	skos:exactMatch	DOID:1517	cecal benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0007198	central nervous system AIDS arteritis	skos:exactMatch	DOID:9005589	AIDS Arteritis, Central Nervous System	semapv:ManualMappingCuration	2023-12-04
EFO:0007199	central nervous system tuberculosis	skos:exactMatch	DOID:1638	central nervous system tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007200	cerebral toxoplasmosis	skos:exactMatch	DOID:9001479	Cerebral Toxoplasmosis	semapv:ManualMappingCuration	2023-12-04
EFO:0007201	cerebral ventricle cancer	skos:exactMatch	DOID:3541	cerebral ventricle cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007202	cervical incompetence	skos:exactMatch	DOID:9681	cervical incompetence	semapv:ManualMappingCuration	2022-01-24
EFO:0007203	cervicofacial actinomycosis	skos:exactMatch	DOID:9008372	Cervicofacial Actinomycosis	semapv:ManualMappingCuration	2023-12-04
EFO:0007204	chickenpox	skos:exactMatch	DOID:8659	chickenpox	semapv:ManualMappingCuration	2022-01-24
EFO:0007205	Chlamydia trachomatis infectious disease	skos:exactMatch	DOID:11263	chlamydia	semapv:ManualMappingCuration	2022-01-24
EFO:0007206	choroid plexus cancer	skos:exactMatch	DOID:3540	choroid plexus cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007207	chromoblastomycosis	skos:exactMatch	DOID:1562	chromoblastomycosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007208	Churg-Strauss syndrome	skos:exactMatch	DOID:3049	Churg-Strauss syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007210	clonorchiasis	skos:exactMatch	DOID:13767	clonorchiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007211	coccidioidomycosis	skos:exactMatch	DOID:13450	coccidioidomycosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007212	coccidiosis	skos:exactMatch	DOID:2113	coccidiosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007213	Colorado tick fever	skos:exactMatch	DOID:4885	Colorado tick fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007214	common cold	skos:exactMatch	DOID:10459	common cold	semapv:ManualMappingCuration	2022-01-24
EFO:0007215	composite lymphoma	skos:exactMatch	DOID:5820	composite lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007216	congenital diaphragmatic hernia	skos:exactMatch	DOID:3827	congenital diaphragmatic hernia	semapv:ManualMappingCuration	2022-01-24
EFO:0007217	congenital nystagmus	skos:exactMatch	DOID:9649	congenital nystagmus	semapv:ManualMappingCuration	2022-01-24
EFO:0007218	congenital rubella	skos:exactMatch	DOID:9001351	Rubella Syndrome, Congenital	semapv:ManualMappingCuration	2023-12-04
EFO:0007219	congenital syphilis	skos:exactMatch	DOID:9856	congenital syphilis	semapv:ManualMappingCuration	2022-01-24
EFO:0007220	congenital toxoplasmosis	skos:exactMatch	DOID:13336	congenital toxoplasmosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007221	contagious pleuropneumonia	skos:exactMatch	DOID:9006515	Contagious Pleuropneumonia	semapv:ManualMappingCuration	2023-12-04
EFO:0007222	contagious pustular dermatitis	skos:exactMatch	DOID:8771	contagious pustular dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007223	Coronaviridae infectious disease	skos:exactMatch	DOID:9001645	Coronaviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007224	coronavirus infectious disease	skos:exactMatch	DOID:0080599	Coronavirus infectious disease	semapv:ManualMappingCuration	2023-12-04
EFO:0007225	cowpox	skos:exactMatch	DOID:8956	cowpox	semapv:ManualMappingCuration	2022-01-24
EFO:0007226	coxsackievirus infectious disease	skos:exactMatch	DOID:9000220	Coxsackievirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007227	croup	skos:exactMatch	DOID:9395	croup	semapv:ManualMappingCuration	2022-01-24
EFO:0007228	cryptococcal meningitis	skos:exactMatch	DOID:0080159	cryptococcal meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007229	cryptococcosis	skos:exactMatch	DOID:12053	cryptococcosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007230	cyclosporiasis	skos:exactMatch	DOID:12750	cyclosporiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007231	cysticercosis	skos:exactMatch	DOID:10079	cysticercosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007232	cystoisosporiasis	skos:exactMatch	DOID:2112	cystoisosporiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007233	diaphragm disease	skos:exactMatch	DOID:10481	diaphragm disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007234	dicrocoeliasis	skos:exactMatch	DOID:1219	dicrocoeliasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007235	Dictyocaulus infectious disease	skos:exactMatch	DOID:9006526	Dictyocaulus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007236	diffuse idiopathic skeletal hyperostosis	skos:exactMatch	DOID:6652	diffuse idiopathic skeletal hyperostosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007237	dipetalonemiasis	skos:exactMatch	DOID:14422	dipetalonemiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007238	diphyllobothriasis	skos:exactMatch	DOID:10075	diphyllobothriasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007239	dirofilariasis	skos:exactMatch	DOID:1082	dirofilariasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007240	dourine	skos:exactMatch	DOID:9002271	Dourine	semapv:ManualMappingCuration	2023-12-04
EFO:0007241	dracunculiasis	skos:exactMatch	DOID:14418	dracunculiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007242	Eastern equine encephalitis	skos:exactMatch	DOID:10841	Eastern equine encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007243	Ebola hemorrhagic fever	skos:exactMatch	DOID:4325	Ebola hemorrhagic fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007244	Ebstein anomaly	skos:exactMatch	DOID:14289	Ebstein anomaly	semapv:ManualMappingCuration	2022-01-24
EFO:0007245	echinococcosis	skos:exactMatch	DOID:1496	echinococcosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007246	echinostomiasis	skos:exactMatch	DOID:1218	echinostomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007247	echovirus infectious disease	skos:exactMatch	DOID:9006823	Echovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007248	egg allergy	skos:exactMatch	DOID:4377	egg allergy	semapv:ManualMappingCuration	2022-01-24
EFO:0007249	emphysematous cholecystitis	skos:exactMatch	DOID:9765	emphysematous cholecystitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007250	encephalitozoonosis	skos:exactMatch	DOID:4270	encephalitozoonosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007251	endocardial fibroelastosis	skos:exactMatch	DOID:12929	endocardial fibroelastosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007252	endodermal sinus tumor	skos:exactMatch	DOID:1911	endodermal sinus tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0007253	Enoplea infectious disease	skos:exactMatch	DOID:9004683	Enoplida Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007254	enterobiasis	skos:exactMatch	DOID:7457	enterobiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007255	Enterovirus infectious disease	skos:exactMatch	DOID:9006549	Enterovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007256	enzootic pneumonia of calves	skos:exactMatch	DOID:9006470	Enzootic Pneumonia of Calves	semapv:ManualMappingCuration	2023-12-04
EFO:0007257	eosinophilic pneumonia	skos:exactMatch	DOID:5870	eosinophilic pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:0007258	ephemeral fever	skos:exactMatch	DOID:9004064	Ephemeral Fever	semapv:ManualMappingCuration	2023-12-04
EFO:0007259	epidemic pleurodynia	skos:exactMatch	DOID:10882	epidemic pleurodynia	semapv:ManualMappingCuration	2022-01-24
EFO:0007260	epidural abscess	skos:exactMatch	DOID:11387	epidural abscess	semapv:ManualMappingCuration	2022-01-24
EFO:0007261	epiglottitis	skos:exactMatch	DOID:9398	epiglottitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007262	epilepsy with generalized tonic-clonic seizures	skos:exactMatch	DOID:7725	epilepsy with generalized tonic-clonic seizures	semapv:ManualMappingCuration	2022-01-24
EFO:0007263	equine infectious anemia	skos:exactMatch	DOID:9003786	Equine Infectious Anemia	semapv:ManualMappingCuration	2023-12-04
EFO:0007264	ethmoid sinusitis	skos:exactMatch	DOID:9507	ethmoid sinusitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007265	eumycotic mycetoma	skos:exactMatch	DOID:13078	eumycotic mycetoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007266	eunuchism	skos:exactMatch	DOID:5003	eunuchism	semapv:ManualMappingCuration	2022-01-24
EFO:0007268	fascioloidiasis	skos:exactMatch	DOID:1217	fascioloidiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007269	Felty's syndrome	skos:exactMatch	DOID:11042	Felty's syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007270	femoral cancer	skos:exactMatch	DOID:5546	femoral cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007271	fibroepithelial neoplasm	skos:exactMatch	DOID:9007017	Fibroepithelial Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0007272	filarial elephantiasis	skos:exactMatch	DOID:12211	filarial elephantiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007273	Filoviridae infectious disease	skos:exactMatch	DOID:9006715	Filoviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007274	Flaviviridae infectious disease	skos:exactMatch	DOID:9008551	Flaviviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007275	focal epithelial hyperplasia	skos:exactMatch	DOID:5362	focal epithelial hyperplasia	semapv:ManualMappingCuration	2022-01-24
EFO:0007276	follicular dendritic cell sarcoma	skos:exactMatch	DOID:6262	follicular dendritic cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007277	foot and mouth disease	skos:exactMatch	DOID:9007040	Foot-and-Mouth Disease	semapv:ManualMappingCuration	2023-12-04
EFO:0007278	fungal lung infectious disease	skos:exactMatch	DOID:9005724	Fungal Lung Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0007279	gas gangrene	skos:exactMatch	DOID:9159	gas gangrene	semapv:ManualMappingCuration	2022-01-24
EFO:0007280	gastrointestinal tuberculosis	skos:exactMatch	DOID:404	gastrointestinal tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007281	geniculate herpes zoster	skos:exactMatch	DOID:9210	herpes zoster oticus	semapv:ManualMappingCuration	2022-01-24
EFO:0007282	genital herpes	skos:exactMatch	DOID:8704	genital herpes	semapv:ManualMappingCuration	2022-01-24
EFO:0007283	geographic tongue	skos:exactMatch	DOID:1455	geographic tongue	semapv:ManualMappingCuration	2022-01-24
EFO:0007284	geotrichosis	skos:exactMatch	DOID:2832	geotrichosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007285	Gerstmann syndrome	skos:exactMatch	DOID:4969	Gerstmann syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007286	glanders	skos:exactMatch	DOID:13444	glanders	semapv:ManualMappingCuration	2022-01-24
EFO:0007287	glucosephosphate dehydrogenase deficiency	skos:exactMatch	DOID:2862	glucosephosphate dehydrogenase deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0007289	gnathomiasis	skos:exactMatch	DOID:11379	gnathomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007290	Goodpasture syndrome	skos:exactMatch	DOID:9808	Goodpasture syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007291	granuloma inguinale	skos:exactMatch	DOID:9113	granuloma inguinale	semapv:ManualMappingCuration	2022-01-24
EFO:0007292	Guillain-Barre syndrome	skos:exactMatch	DOID:12842	Guillain-Barre syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007293	haemonchiasis	skos:exactMatch	DOID:3332	haemonchiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007294	hand, foot and mouth disease	skos:exactMatch	DOID:10881	hand, foot and mouth disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007295	Hantavirus infectious disease	skos:exactMatch	DOID:9007533	Hantavirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007296	hantavirus pulmonary syndrome	skos:exactMatch	DOID:14472	hantavirus pulmonary syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007297	HELLP syndrome	skos:exactMatch	DOID:13133	HELLP syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007298	hemopericardium	skos:exactMatch	DOID:11482	hemopericardium	semapv:ManualMappingCuration	2022-01-24
EFO:0007299	hemorrhagic fever with renal syndrome	skos:exactMatch	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007300	Henipavirus infectious disease	skos:exactMatch	DOID:9001406	Henipavirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007301	Hepadnaviridae infectious disease	skos:exactMatch	DOID:9004126	Hepadnaviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007302	hepatic tuberculosis	skos:exactMatch	DOID:407	hepatic tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007303	hepatitis E virus infection	skos:exactMatch	DOID:4411	hepatitis E	semapv:ManualMappingCuration	2022-01-24
EFO:0007304	hepatitis D virus infection	skos:exactMatch	DOID:2047	hepatitis D	semapv:ManualMappingCuration	2022-01-24
EFO:0007305	hepatitis A virus infection	skos:exactMatch	DOID:12549	hepatitis A	semapv:ManualMappingCuration	2022-01-24
EFO:0007306	herpangina	skos:exactMatch	DOID:10883	herpangina	semapv:ManualMappingCuration	2022-01-24
EFO:0007307	Herpes simplex virus gingivostomatitis	skos:exactMatch	DOID:9008291	Herpetic Stomatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0007308	Herpes simplex virus keratitis	skos:exactMatch	DOID:0080158	herpes simplex virus keratitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007309	Herpesviridae infectious disease	skos:exactMatch	DOID:9002834	Herpesviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007310	histoplasmosis	skos:exactMatch	DOID:1731	histoplasmosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007311	HIV enteropathy	skos:exactMatch	DOID:9002094	HIV Enteropathy	semapv:ManualMappingCuration	2023-12-04
EFO:0007312	HIV wasting syndrome	skos:exactMatch	DOID:9000540	HIV Wasting Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0007313	HIV-associated nephropathy	skos:exactMatch	DOID:9008782	AIDS-Associated Nephropathy	semapv:ManualMappingCuration	2023-12-04
EFO:0007314	hookworm infectious disease	skos:exactMatch	DOID:9006535	Hookworm Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007315	hordeolum	skos:exactMatch	DOID:9909	hordeolum	semapv:ManualMappingCuration	2022-01-24
EFO:0007316	Human T-lymphotropic virus 1 infectious disease	skos:exactMatch	DOID:9002670	HTLV-I Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007317	hymenolepiasis	skos:exactMatch	DOID:10074	hymenolepiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007318	hyperinsulinemic hypoglycemia	skos:exactMatch	DOID:13317	hyperinsulinemic hypoglycemia	semapv:ManualMappingCuration	2022-01-24
EFO:0007319	hyperprolactinemia	skos:exactMatch	DOID:12700	hyperprolactinemia	semapv:ManualMappingCuration	2022-01-24
EFO:0007320	hypodermyiasis	skos:exactMatch	DOID:12926	hypodermyiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007321	hypopharynx cancer	skos:exactMatch	DOID:8533	hypopharynx cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007322	idiopathic CD4-positive T-lymphocytopenia	skos:exactMatch	DOID:3109	idiopathic CD4-positive T-lymphocytopenia	semapv:ManualMappingCuration	2022-01-24
EFO:0007323	inclusion body myositis	skos:exactMatch	DOID:3429	inclusion body myositis	semapv:ManualMappingCuration	2022-01-24
EFO:0007324	inclusion conjunctivitis	skos:exactMatch	DOID:13800	inclusion conjunctivitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007325	infectious ectromelia	skos:exactMatch	DOID:9002137	Infectious Ectromelia	semapv:ManualMappingCuration	2023-12-04
EFO:0007326	infectious mononucleosis	skos:exactMatch	DOID:8568	infectious mononucleosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007327	infectious myxomatosis	skos:exactMatch	DOID:9002518	Infectious Myxomatosis	semapv:ManualMappingCuration	2023-12-04
EFO:0007328	influenza	skos:exactMatch	DOID:8469	influenza	semapv:ManualMappingCuration	2022-01-24
EFO:0007328	influenza	skos:exactMatch	DOID:9001488	Human Influenza	semapv:ManualMappingCuration	2023-12-04
EFO:0007329	interdigitating dendritic cell sarcoma	skos:exactMatch	DOID:7848	interdigitating dendritic cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007330	intestinal cancer	skos:exactMatch	DOID:10155	intestinal cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007331	islet cell tumor	skos:exactMatch	DOID:1799	islet cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0007332	Japanese encephalitis	skos:exactMatch	DOID:10844	Japanese encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007333	jaw cancer	skos:exactMatch	DOID:1862	jaw cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007335	Kluver-Bucy syndrome	skos:exactMatch	DOID:2510	Kluver-Bucy syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007336	Langerhans cell sarcoma	skos:exactMatch	DOID:7146	Langerhans cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007337	laryngeal tuberculosis	skos:exactMatch	DOID:1583	laryngeal tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007338	Lassa fever	skos:exactMatch	DOID:9537	Lassa fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007339	late congenital syphilis	skos:exactMatch	DOID:10039	late congenital syphilis	semapv:ManualMappingCuration	2022-01-24
EFO:0007340	latent syphilis	skos:exactMatch	DOID:9531	latent syphilis	semapv:ManualMappingCuration	2022-01-24
EFO:0007342	legionellosis	skos:exactMatch	DOID:10458	legionellosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007343	Legionnaires' disease	skos:exactMatch	DOID:10457	Legionnaires' disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007344	leptospirosis	skos:exactMatch	DOID:2297	leptospirosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007345	lipid pneumonia	skos:exactMatch	DOID:3241	lipid pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:0007346	lipoatrophic diabetes	skos:exactMatch	DOID:11712	lipoatrophic diabetes mellitus	semapv:ManualMappingCuration	2022-01-24
EFO:0007347	listeriosis	skos:exactMatch	DOID:11573	listeriosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007348	louping ill	skos:exactMatch	DOID:10250	louping ill	semapv:ManualMappingCuration	2022-01-24
EFO:0007349	lumpy skin disease	skos:exactMatch	DOID:9005597	Lumpy Skin Disease	semapv:ManualMappingCuration	2023-12-04
EFO:0007350	lymph node tuberculosis	skos:exactMatch	DOID:4889	lymph node tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007351	lymphangitis	skos:exactMatch	DOID:9317	lymphangitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007352	lymphatic system disease	skos:exactMatch	DOID:75	lymphatic system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007353	lymphogranuloma venereum	skos:exactMatch	DOID:13819	lymphogranuloma venereum	semapv:ManualMappingCuration	2022-01-24
EFO:0007355	male reproductive organ cancer	skos:exactMatch	DOID:3856	male reproductive organ cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007356	mandibular cancer	skos:exactMatch	DOID:2338	mandibular cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007357	mansonelliasis	skos:exactMatch	DOID:1081	mansonelliasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007358	Marburg hemorrhagic fever	skos:exactMatch	DOID:4327	Marburg hemorrhagic fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007359	mast-cell leukemia	skos:exactMatch	DOID:9254	mast-cell leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:0007360	maxillary neoplasm	skos:exactMatch	DOID:4618	maxillary cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007360	maxillary neoplasm	skos:exactMatch	DOID:9002201	Maxillary Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0007361	maxillary sinusitis	skos:exactMatch	DOID:2051	maxillary sinusitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007362	mediastinal cancer	skos:exactMatch	DOID:5559	mediastinal cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007363	meibomian cyst	skos:exactMatch	DOID:9903	meibomian cyst	semapv:ManualMappingCuration	2022-01-24
EFO:0007364	meningoencephalitis	skos:exactMatch	DOID:10554	meningoencephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007365	mesoblastic nephroma	skos:exactMatch	DOID:4773	congenital mesoblastic nephroma	semapv:ManualMappingCuration	2023-12-04
EFO:0007366	microsporidiosis	skos:exactMatch	DOID:4271	microsporidiosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007367	middle lobe syndrome	skos:exactMatch	DOID:2810	middle lobe syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007368	miliary tuberculosis	skos:exactMatch	DOID:9861	miliary tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007369	milk allergic reaction	skos:exactMatch	DOID:4376	milk allergy	semapv:ManualMappingCuration	2022-01-24
EFO:0007370	milker's nodule	skos:exactMatch	DOID:8729	milker's nodule	semapv:ManualMappingCuration	2022-01-24
EFO:0007371	Miller Fisher syndrome	skos:exactMatch	DOID:12889	Miller Fisher syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007372	mitral valve stenosis	skos:exactMatch	DOID:1754	mitral valve stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007373	mixed cell type cancer	skos:exactMatch	DOID:154	mixed cell type cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007374	mixed connective tissue disease	skos:exactMatch	DOID:3492	mixed connective tissue disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007375	molluscum contagiosum	skos:exactMatch	DOID:8867	molluscum contagiosum	semapv:ManualMappingCuration	2022-01-24
EFO:0007376	Mononegavirales infectious disease	skos:exactMatch	DOID:9007829	Mononegavirales Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007377	Morbillivirus infectious disease	skos:exactMatch	DOID:9003860	Morbillivirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007378	mucinous cystadenocarcinoma	skos:exactMatch	DOID:3603	mucinous cystadenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007379	mucocutaneous Leishmaniasis	skos:exactMatch	DOID:9155	mucocutaneous leishmaniasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007380	mucormycosis	skos:exactMatch	DOID:8485	mucormycosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007381	multidrug-resistant tuberculosis	skos:exactMatch	DOID:401	multidrug-resistant tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007382	multiple chemical sensitivity	skos:exactMatch	DOID:4661	multiple chemical sensitivity	semapv:ManualMappingCuration	2022-01-24
EFO:0007383	Mumps virus infectious disease	skos:exactMatch	DOID:10264	mumps	semapv:ManualMappingCuration	2022-01-24
EFO:0007384	muscle cancer	skos:exactMatch	DOID:4045	muscle cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007385	mushroom workers' lung	skos:exactMatch	DOID:2708	mushroom workers' lung	semapv:ManualMappingCuration	2022-01-24
EFO:0007386	Mycobacterium avium complex disease	skos:exactMatch	DOID:2755	Mycobacterium avium complex disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007387	Mycoplasma pneumoniae pneumonia	skos:exactMatch	DOID:13276	Mycoplasma pneumoniae pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:0007388	myelophthisic anemia	skos:exactMatch	DOID:2354	myelophthisic anemia	semapv:ManualMappingCuration	2022-01-24
EFO:0007389	myiasis	skos:exactMatch	DOID:11080	myiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007390	necatoriasis	skos:exactMatch	DOID:2790	necatoriasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007391	Nematoda infectious disease	skos:exactMatch	DOID:9002992	Nematode Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007392	nervous system cancer	skos:exactMatch	DOID:3093	nervous system cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007393	neuroaspergillosis	skos:exactMatch	DOID:13565	neuroaspergillosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007394	neuroschistosomiasis	skos:exactMatch	DOID:13722	neuroschistosomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007395	Newcastle disease	skos:exactMatch	DOID:2929	Newcastle disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007396	Nidovirales infectious disease	skos:exactMatch	DOID:9008504	Nidovirales Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007397	nocardiosis	skos:exactMatch	DOID:2312	nocardiosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007398	ocular onchocerciasis	skos:exactMatch	DOID:9007599	Ocular Onchocerciasis	semapv:ManualMappingCuration	2023-12-04
EFO:0007399	ocular toxoplasmosis	skos:exactMatch	DOID:9004945	Ocular Toxoplasmosis	semapv:ManualMappingCuration	2023-12-04
EFO:0007400	oesophagostomiasis	skos:exactMatch	DOID:3983	oesophagostomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007401	oligohydramnios	skos:exactMatch	DOID:12215	oligohydramnios	semapv:ManualMappingCuration	2022-01-24
EFO:0007402	onchocerciasis	skos:exactMatch	DOID:11678	onchocerciasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007403	ophthalmic herpes zoster	skos:exactMatch	DOID:9004854	Herpes Zoster Ophthalmicus	semapv:ManualMappingCuration	2023-12-04
EFO:0007404	opisthorchiasis	skos:exactMatch	DOID:13768	opisthorchiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007405	optic neuritis	skos:exactMatch	DOID:1210	optic neuritis	semapv:ManualMappingCuration	2022-01-24
EFO:0007406	oral candidiasis	skos:exactMatch	DOID:14262	oral candidiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007407	oral tuberculosis	skos:exactMatch	DOID:402	oral tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007408	orbital cancer	skos:exactMatch	DOID:4143	orbital cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007409	Ornithine transcarbamylase deficiency	skos:exactMatch	DOID:9271	ornithine carbamoyltransferase deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0007410	ornithosis	skos:exactMatch	DOID:11262	ornithosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007411	Orthomyxoviridae infectious disease	skos:exactMatch	DOID:9001499	Orthomyxoviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007412	ossifying fibroma	skos:exactMatch	DOID:180	ossifying fibroma	semapv:ManualMappingCuration	2022-01-24
EFO:0007413	osteitis fibrosa	skos:exactMatch	DOID:3341	osteitis fibrosa	semapv:ManualMappingCuration	2022-01-24
EFO:0007414	ostertagiasis	skos:exactMatch	DOID:3985	ostertagiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007415	otitis media with effusion	skos:exactMatch	DOID:9008821	Otitis Media with Effusion	semapv:ManualMappingCuration	2023-12-04
EFO:0007416	pancreatic endocrine carcinoma	skos:exactMatch	DOID:1798	pancreatic endocrine carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007417	paracoccidioidomycosis	skos:exactMatch	DOID:12662	paracoccidioidomycosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007418	paragonimiasis	skos:exactMatch	DOID:10699	paragonimiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007419	Paramyxoviridae infectious disease	skos:exactMatch	DOID:9007244	Paramyxoviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007420	paratyphoid fever	skos:exactMatch	DOID:3055	paratyphoid fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007421	paronychia	skos:exactMatch	DOID:13117	paronychia	semapv:ManualMappingCuration	2022-01-24
EFO:0007422	parotid disease	skos:exactMatch	DOID:10302	parotid disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007423	parotitis	skos:exactMatch	DOID:10301	parotitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007424	pasteurellosis	skos:exactMatch	DOID:11055	pasteurellosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007425	peanut allergic reaction	skos:exactMatch	DOID:4378	peanut allergy	semapv:ManualMappingCuration	2022-01-24
EFO:0007426	pericardial tuberculosis	skos:exactMatch	DOID:4962	pericardial tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007427	pericarditis	skos:exactMatch	DOID:1787	pericarditis	semapv:ManualMappingCuration	2022-01-24
EFO:0007428	periodic limb movement disorder	skos:exactMatch	DOID:9207	periodic limb movement disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0007429	peritonsillar abscess	skos:exactMatch	DOID:9002456	Peritonsillar Abscess	semapv:ManualMappingCuration	2023-12-04
EFO:0007430	persian gulf syndrome	skos:exactMatch	DOID:4491	persian gulf syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007431	peste des petits ruminants infectious disease	skos:exactMatch	DOID:9005375	Peste-des-Petits-Ruminants	semapv:ManualMappingCuration	2023-12-04
EFO:0007432	Pestivirus infectious disease	skos:exactMatch	DOID:9008833	Pestivirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007433	phagocyte bactericidal dysfunction	skos:exactMatch	DOID:3262	phagocyte bactericidal dysfunction	semapv:ManualMappingCuration	2022-01-24
EFO:0007434	pharyngoconjunctival fever	skos:exactMatch	DOID:13801	pharyngoconjunctival fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007436	phencyclidine abuse	skos:exactMatch	DOID:5062	phencyclidine abuse	semapv:ManualMappingCuration	2022-01-24
EFO:0007437	Phlebotomus fever	skos:exactMatch	DOID:11360	Phlebotomus fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007438	Picornaviridae infectious disease	skos:exactMatch	DOID:9003470	Picornaviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007439	pityriasis versicolor	skos:exactMatch	DOID:9060	pityriasis versicolor	semapv:ManualMappingCuration	2022-01-24
EFO:0007440	placenta accreta	skos:exactMatch	DOID:4744	placenta accreta	semapv:ManualMappingCuration	2022-01-24
EFO:0007441	placenta disease	skos:exactMatch	DOID:780	placenta disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007442	placenta praevia	skos:exactMatch	DOID:11060	placenta praevia	semapv:ManualMappingCuration	2022-01-24
EFO:0007443	placental insufficiency	skos:exactMatch	DOID:3891	placental insufficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0007444	Plasmodium falciparum malaria	skos:exactMatch	DOID:14067	Plasmodium falciparum malaria	semapv:ManualMappingCuration	2022-01-24
EFO:0007445	Plasmodium vivax malaria	skos:exactMatch	DOID:12978	Plasmodium vivax malaria	semapv:ManualMappingCuration	2022-01-24
EFO:0007446	pleural tuberculosis	skos:exactMatch	DOID:106	pleural tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007447	Pneumocystis infectious disease	skos:exactMatch	DOID:9007019	Pneumocystis Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007448	pneumocystosis	skos:exactMatch	DOID:11339	pneumocystosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007449	pneumonic pasteurellosis	skos:exactMatch	DOID:9008774	Pneumonic Pasteurellosis	semapv:ManualMappingCuration	2023-12-04
EFO:0007450	poliomyelitis	skos:exactMatch	DOID:4953	poliomyelitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007451	Polyomavirus infectious disease	skos:exactMatch	DOID:9000386	Polyomavirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007452	post-thrombotic syndrome	skos:exactMatch	DOID:2364	post-thrombotic syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007453	postpartum depression	skos:exactMatch	DOID:9478	postpartum depression	semapv:ManualMappingCuration	2022-01-24
EFO:0007454	postpoliomyelitis syndrome	skos:exactMatch	DOID:4952	postpoliomyelitis syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007455	progressive multifocal leukoencephalopathy	skos:exactMatch	DOID:643	progressive multifocal leukoencephalopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0007456	pseudomyxoma peritonei	skos:exactMatch	DOID:3559	pseudomyxoma peritonei	semapv:ManualMappingCuration	2022-01-24
EFO:0007457	pseudorabies	skos:exactMatch	DOID:9002204	Pseudorabies	semapv:ManualMappingCuration	2023-12-04
EFO:0007458	pulmonary blastoma	skos:exactMatch	DOID:4765	pulmonary blastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007459	pyruvate decarboxylase deficiency	skos:exactMatch	DOID:3649	pyruvate decarboxylase deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:0007460	reactive arthritis	skos:exactMatch	DOID:6196	reactive arthritis	semapv:ManualMappingCuration	2022-01-24
EFO:0007462	REM sleep behavior disorder	skos:exactMatch	DOID:9091	REM sleep behavior disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0007463	renal tuberculosis	skos:exactMatch	DOID:9733	renal tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007464	Reoviridae infectious disease	skos:exactMatch	DOID:9006487	Reoviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007465	Respirovirus infectious disease	skos:exactMatch	DOID:9008225	Respirovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007466	retroperitoneal cancer	skos:exactMatch	DOID:5875	retroperitoneal cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007467	Reye syndrome	skos:exactMatch	DOID:14525	Reye syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007468	Rhabditida infectious disease	skos:exactMatch	DOID:9001387	Rhabditida Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007469	Rhabdoviridae infectious disease	skos:exactMatch	DOID:9008603	Rhabdoviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007470	rhinoscleroma	skos:exactMatch	DOID:11336	rhinoscleroma	semapv:ManualMappingCuration	2022-01-24
EFO:0007471	rhinosporidiosis	skos:exactMatch	DOID:2409	rhinosporidiosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007472	rickettsial pneumonia	skos:exactMatch	DOID:9006977	Rickettsial Pneumonia	semapv:ManualMappingCuration	2023-12-04
EFO:0007473	Ritter's disease	skos:exactMatch	DOID:9063	Ritter's disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007474	Roseolovirus infectious disease	skos:exactMatch	DOID:9002501	Roseolovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007475	Salmonella gastroenteritis	skos:exactMatch	DOID:9003664	Salmonella Food Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:0007476	sarcocystosis	skos:exactMatch	DOID:9640	sarcocystosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007477	scarlet fever	skos:exactMatch	DOID:8596	scarlet fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007478	scirrhous adenocarcinoma	skos:exactMatch	DOID:4024	scirrhous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007479	screw worm infectious disease	skos:exactMatch	DOID:12927	screw worm infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:0007480	scrub typhus	skos:exactMatch	DOID:13371	scrub typhus	semapv:ManualMappingCuration	2022-01-24
EFO:0007481	septicemic plague	skos:exactMatch	DOID:3481	septicemic plague	semapv:ManualMappingCuration	2022-01-24
EFO:0007482	setariasis	skos:exactMatch	DOID:1079	setariasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007484	sick building syndrome	skos:exactMatch	DOID:2710	sick building syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007485	silicosis	skos:exactMatch	DOID:10325	silicosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007486	sinusitis	skos:exactMatch	DOID:0050127	sinusitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007487	skeletal tuberculosis	skos:exactMatch	DOID:1639	skeletal tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007488	sparganosis	skos:exactMatch	DOID:10080	sparganosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007489	sphenoid sinusitis	skos:exactMatch	DOID:10794	sphenoid sinusitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007490	spinal stenosis	skos:exactMatch	DOID:6725	spinal stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007491	spleen cancer	skos:exactMatch	DOID:672	spleen cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007492	splenic tuberculosis	skos:exactMatch	DOID:9305	splenic tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007493	spondylolisthesis	skos:exactMatch	DOID:6682	spondylolisthesis	semapv:ManualMappingCuration	2022-01-24
EFO:0007494	sporotrichosis	skos:exactMatch	DOID:14484	sporotrichosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007495	St. Louis encephalitis	skos:exactMatch	DOID:10845	St. Louis encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007496	staphylococcal pneumonia	skos:exactMatch	DOID:9001049	Staphylococcal Pneumonia	semapv:ManualMappingCuration	2023-12-04
EFO:0007497	staphyloenterotoxemia	skos:exactMatch	DOID:96	staphyloenterotoxemia	semapv:ManualMappingCuration	2022-01-24
EFO:0007498	Stiff-Person syndrome	skos:exactMatch	DOID:13366	Stiff-Person syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007499	streptococcal pneumonia	skos:exactMatch	DOID:0040084	Streptococcus pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:0007500	Strongylida infectious disease	skos:exactMatch	DOID:9003369	Strongylida Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007501	strongyloidiasis	skos:exactMatch	DOID:10955	strongyloidiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007502	subacute sclerosing panencephalitis	skos:exactMatch	DOID:8970	subacute sclerosing panencephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007503	suppurative otitis media	skos:exactMatch	DOID:11506	suppurative otitis media	semapv:ManualMappingCuration	2022-01-24
EFO:0007504	syphilis	skos:exactMatch	DOID:4166	syphilis	semapv:ManualMappingCuration	2022-01-24
EFO:0007505	tabes dorsalis	skos:exactMatch	DOID:10027	tabes dorsalis	semapv:ManualMappingCuration	2022-01-24
EFO:0007506	theileriasis	skos:exactMatch	DOID:3733	theileriasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007507	thoracic outlet syndrome	skos:exactMatch	DOID:3103	thoracic outlet syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007508	tick infestation	skos:exactMatch	DOID:4109	tick infestation	semapv:ManualMappingCuration	2022-01-24
EFO:0007509	tick paralysis	skos:exactMatch	DOID:11285	tick paralysis	semapv:ManualMappingCuration	2022-01-24
EFO:0007510	tinea	skos:exactMatch	DOID:8913	dermatophytosis	semapv:ManualMappingCuration	2023-12-04
EFO:0007511	tinea favosa	skos:exactMatch	DOID:4336	tinea favosa	semapv:ManualMappingCuration	2022-01-24
EFO:0007512	tinea pedis	skos:exactMatch	DOID:12403	tinea pedis	semapv:ManualMappingCuration	2022-01-24
EFO:0007513	Togaviridae infectious disease	skos:exactMatch	DOID:9002987	Togaviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007514	Torovirus infectious disease	skos:exactMatch	DOID:9000501	Torovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0007515	toxascariasis	skos:exactMatch	DOID:3107	toxascariasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007516	toxocariasis	skos:exactMatch	DOID:9790	toxocariasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007517	toxoplasmosis	skos:exactMatch	DOID:9965	toxoplasmosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007518	tracheitis	skos:exactMatch	DOID:9392	tracheitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007519	trench fever	skos:exactMatch	DOID:11101	trench fever	semapv:ManualMappingCuration	2022-01-24
EFO:0007520	trichinosis	skos:exactMatch	DOID:9784	trichinosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007521	Trichomonas vaginitis	skos:exactMatch	DOID:0050269	Trichomonas vaginalis trichomoniasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007522	trichostrongyloidiasis	skos:exactMatch	DOID:1255	trichostrongyloidiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007523	trichostrongylosis	skos:exactMatch	DOID:1254	trichostrongylosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007524	trichuriasis	skos:exactMatch	DOID:1252	trichuriasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007525	tricuspid valve stenosis	skos:exactMatch	DOID:4078	tricuspid valve stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007526	trombiculiasis	skos:exactMatch	DOID:8399	trombiculiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007527	tropical spastic paraparesis	skos:exactMatch	DOID:321	tropical spastic paraparesis	semapv:ManualMappingCuration	2022-01-24
EFO:0007528	tuberculous empyema	skos:exactMatch	DOID:14305	tuberculous empyema	semapv:ManualMappingCuration	2022-01-24
EFO:0007529	tuberculous peritonitis	skos:exactMatch	DOID:9801	tuberculous peritonitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007530	urinary schistosomiasis	skos:exactMatch	DOID:1394	urinary schistosomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007531	urogenital tuberculosis	skos:exactMatch	DOID:2149	urogenital tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:0007532	uterine corpus cancer	skos:exactMatch	DOID:9460	uterine corpus cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0007533	vasomotor rhinitis	skos:exactMatch	DOID:4730	vasomotor rhinitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007534	Venezuelan equine encephalitis	skos:exactMatch	DOID:9584	Venezuelan equine encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007535	verrucous carcinoma	skos:exactMatch	DOID:3737	verrucous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0007536	vesicoureteral reflux	skos:exactMatch	DOID:9620	vesicoureteral reflux	semapv:ManualMappingCuration	2022-01-24
EFO:0007537	vestibular neuronitis	skos:exactMatch	DOID:12683	vestibular neuronitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007538	viral encephalitis	skos:exactMatch	DOID:646	viral encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007539	viral hemorrhagic septicemia	skos:exactMatch	DOID:9004664	Viral Hemorrhagic Septicemia	semapv:ManualMappingCuration	2023-12-04
EFO:0007540	animal viral hepatitis	skos:exactMatch	DOID:1884	viral hepatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007540	animal viral hepatitis	skos:exactMatch	DOID:9007899	Animal Viral Hepatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0007541	viral pneumonia	skos:exactMatch	DOID:10533	viral pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:0007542	visna	skos:exactMatch	DOID:9004261	Visna	semapv:ManualMappingCuration	2023-12-04
EFO:0007543	vulvovaginal candidiasis	skos:exactMatch	DOID:2272	vulvovaginal candidiasis	semapv:ManualMappingCuration	2022-01-24
EFO:0007544	Waterhouse-Friderichsen syndrome	skos:exactMatch	DOID:9931	Waterhouse-Friderichsen syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007545	West Nile encephalitis	skos:exactMatch	DOID:2365	West Nile encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007546	Western equine encephalitis	skos:exactMatch	DOID:10843	Western equine encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:0007547	Wissler's syndrome	skos:exactMatch	DOID:3047	Wissler-Fanconi syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007548	yaws	skos:exactMatch	DOID:10371	yaws	semapv:ManualMappingCuration	2022-01-24
EFO:0007549	Zollinger-Ellison Syndrome	skos:exactMatch	DOID:0050782	Zollinger-Ellison syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0007625	asthenia	skos:exactMatch	DOID:9003000	Asthenia	semapv:ManualMappingCuration	2023-12-04
EFO:0007634	major depressive episode	skos:exactMatch	DOID:1470	major depressive disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0007685	trichloroethylene-induced hypersensitivity	skos:exactMatch	DOID:9008261	Chemically-Induced Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0007686	surgical shock	skos:exactMatch	DOID:9000618	Surgical Shock	semapv:ManualMappingCuration	2023-12-04
EFO:0007879	petaloid toenail	skos:exactMatch	DOID:9002206	Double Nail for Fifth Toe	semapv:ManualMappingCuration	2023-12-04
EFO:0007887	autosomal dominant compelling helio-ophthalmic outburst syndrome	skos:exactMatch	DOID:9003596	Autosomal Dominant Compelling Helio Ophthalmic Outburst Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0007926	hyper-inflammatory immune response	skos:exactMatch	DOID:2914	immune system disease	semapv:ManualMappingCuration	2023-12-04
EFO:0007940	chronic venous insufficiency	skos:exactMatch	DOID:0050853	chronic venous insufficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0007948	HIV-associated neurocognitive disorder	skos:exactMatch	DOID:9004086	AIDS Dementia Complex	semapv:ManualMappingCuration	2023-12-04
EFO:0007949	acute-on-chronic liver failure	skos:exactMatch	DOID:9000238	Acute-On-Chronic Liver Failure	semapv:ManualMappingCuration	2023-12-04
EFO:0007982	mild neurocognitive disorder	skos:exactMatch	DOID:0080832	mild cognitive impairment	semapv:ManualMappingCuration	2023-12-04
EFO:0008008	lower urinary tract symptom	skos:exactMatch	DOID:9003962	Lower Urinary Tract Symptoms	semapv:ManualMappingCuration	2023-12-04
EFO:0008349	thiazide-induced hyponatremia	skos:exactMatch	DOID:9006635	Hyponatremia	semapv:ManualMappingCuration	2023-12-04
EFO:0008462	pregnancy induced alloimmunization	skos:exactMatch	DOID:4175	Rh isoimmunization	semapv:ManualMappingCuration	2023-12-04
EFO:0008490	ampulla of Vater adenocarcinoma	skos:exactMatch	DOID:3502	ampulla of Vater adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008491	atypical ductal hyperplasia	skos:exactMatch	DOID:0060074	ductal carcinoma in situ	semapv:ManualMappingCuration	2023-12-04
EFO:0008492	breast hyperplasia	skos:exactMatch	DOID:9000937	breast hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0008493	cerebral small vessel disease	skos:exactMatch	DOID:0112313	brain small vessel disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008495	childhood supratentorial ependymoma	skos:exactMatch	DOID:7502	childhood supratentorial ependymoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008496	chronic hepatitis	skos:exactMatch	DOID:9008510	Chronic Hepatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0008497	chronic lung allograft dysfunction	skos:exactMatch	DOID:9007461	Chronic Lung Allograft Dysfunction	semapv:ManualMappingCuration	2023-12-04
EFO:0008498	clear cell sarcoma	skos:exactMatch	DOID:4233	clear cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008499	DNA repair deficiency	skos:exactMatch	DOID:9008840	DNA Repair-Deficiency Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0008500	ductal breast hyperplasia	skos:exactMatch	DOID:9004693	ductal breast hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0008502	gastric non-cardia carcinoma	skos:exactMatch	DOID:5517	stomach carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0008503	hepatitis B virus induced hepatocellular carcinoma	skos:exactMatch	DOID:684	hepatocellular carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0008504	hepatitis C virus induced hepatocellular carcinoma	skos:exactMatch	DOID:684	hepatocellular carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0008505	hepatitis virus-related hepatocellular carcinoma	skos:exactMatch	DOID:684	hepatocellular carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0008506	hyperparathyroidism	skos:exactMatch	DOID:13543	hyperparathyroidism	semapv:ManualMappingCuration	2022-01-24
EFO:0008507	interstitial cystitis	skos:exactMatch	DOID:13949	interstitial cystitis	semapv:ManualMappingCuration	2022-01-24
EFO:0008507	interstitial cystitis	skos:exactMatch	DOID:1678	chronic interstitial cystitis	semapv:ManualMappingCuration	2022-01-24
EFO:0008508	large cell medulloblastoma	skos:exactMatch	DOID:3857	large cell medulloblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008509	lobular breast carcinoma	skos:exactMatch	DOID:0050938	breast lobular carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008510	Lyme disease	skos:exactMatch	DOID:11729	Lyme disease	semapv:ManualMappingCuration	2022-01-24
EFO:0008511	metopic craniosynostosis	skos:exactMatch	DOID:9007261	Nonsyndromic Trigonocephaly	semapv:ManualMappingCuration	2023-12-04
EFO:0008512	micropapillary urothelial carcinoma	skos:exactMatch	DOID:6976	micropapillary variant infiltrating bladder urothelial carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008514	neurofibromatosis	skos:exactMatch	DOID:8712	neurofibromatosis	semapv:ManualMappingCuration	2022-01-24
EFO:0008515	nodular melanoma	skos:exactMatch	DOID:10047	nodular malignant melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008516	non-functioning pituitary adenoma	skos:exactMatch	DOID:5715	functionless pituitary adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008517	oral lichen planus	skos:exactMatch	DOID:9003036	Oral Lichen Planus	semapv:ManualMappingCuration	2023-12-04
EFO:0008518	polymyalgia rheumatica	skos:exactMatch	DOID:853	polymyalgia rheumatica	semapv:ManualMappingCuration	2022-01-24
EFO:0008519	primary hyperparathyroidism	skos:exactMatch	DOID:11202	primary hyperparathyroidism	semapv:ManualMappingCuration	2022-01-24
EFO:0008520	primary progressive multiple sclerosis	skos:exactMatch	DOID:0050784	primary progressive multiple sclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0008521	rhinitis	skos:exactMatch	DOID:4483	rhinitis	semapv:ManualMappingCuration	2022-01-24
EFO:0008522	secondary progressive multiple sclerosis	skos:exactMatch	DOID:0050783	secondary progressive multiple sclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0008524	small cell carcinoma	skos:exactMatch	DOID:0050685	small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0008525	spinal muscular atrophy	skos:exactMatch	DOID:12377	spinal muscular atrophy	semapv:ManualMappingCuration	2022-01-24
EFO:0008526	status epilepticus	skos:exactMatch	DOID:1824	status epilepticus	semapv:ManualMappingCuration	2022-01-24
EFO:0008527	steatosis	skos:exactMatch	DOID:9455	lipid storage disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008528	urothelial carcinoma	skos:exactMatch	DOID:2671	transitional cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0008532	clinically amyopathic dermatomyositis	skos:exactMatch	DOID:9005507	Amyopathic Dermatomyositis	semapv:ManualMappingCuration	2023-12-04
EFO:0008533	dyspepsia	skos:exactMatch	DOID:9001204	Dyspepsia	semapv:ManualMappingCuration	2023-12-04
EFO:0008536	anti-centromere-antibody-positive systemic scleroderma	skos:exactMatch	DOID:418	systemic scleroderma	semapv:ManualMappingCuration	2023-12-04
EFO:0008537	anti-topoisomerase-I-antibody-positive systemic scleroderma	skos:exactMatch	DOID:418	systemic scleroderma	semapv:ManualMappingCuration	2023-12-04
EFO:0008545	Malignant Breast Phyllodes Tumor	skos:exactMatch	DOID:3016	breast malignant phyllodes tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0008546	poisoning	skos:exactMatch	DOID:9000046	Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:0008549	digestive system neoplasm	skos:exactMatch	DOID:9004351	Digestive System Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0008550	Hepatobiliary Neoplasm	skos:exactMatch	DOID:0080355	hepatobiliary system cancer	semapv:ManualMappingCuration	2023-04-17
EFO:0008550	Hepatobiliary Neoplasm	skos:exactMatch	DOID:3117	hepatobiliary benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0008553	femur fracture	skos:exactMatch	DOID:9008763	Femoral Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0008555	Methicillin-Resistant Staphylococcus Aureus Infection	skos:exactMatch	DOID:9007315	Methicillin-Resistant Staphylococcus Aureus Infection	semapv:ManualMappingCuration	2023-12-04
EFO:0008556	Methicillin-Resistant Staphylococcus Aureus Pneumonia	skos:exactMatch	DOID:9001049	Staphylococcal Pneumonia	semapv:ManualMappingCuration	2023-12-04
EFO:0008557	Methicillin-Susceptible Staphylococcus Aureus Infection	skos:exactMatch	DOID:9008885	Staphylococcal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0008558	Vancomycin-Resistant Staphylococcus Aureus Infection	skos:exactMatch	DOID:9008885	Staphylococcal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0008559	American trypanosomiasis	skos:exactMatch	DOID:12140	Chagas disease	semapv:ManualMappingCuration	2022-01-24
EFO:0008560	female infertility	skos:exactMatch	DOID:9007456	Female Infertility	semapv:ManualMappingCuration	2023-12-04
EFO:0008561	diaphragmatic hernia	skos:exactMatch	DOID:9009073	Diaphragmatic Hernia	semapv:ManualMappingCuration	2023-12-04
EFO:0008568	Sleep Disorder	skos:exactMatch	DOID:535	sleep disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0008569	Thiamine deficiency	skos:exactMatch	DOID:0070313	thiamine deficiency disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008570	Vitamin B3 deficiency	skos:exactMatch	DOID:8457	pellagra	semapv:ManualMappingCuration	2023-12-04
EFO:0008571	viral conjunctivitis	skos:exactMatch	DOID:9000608	Viral Conjunctivitis	semapv:ManualMappingCuration	2023-12-04
EFO:0008572	malnutrition	skos:exactMatch	DOID:9005695	Malnutrition	semapv:ManualMappingCuration	2023-12-04
EFO:0008573	alcoholic liver disease	skos:exactMatch	DOID:9001285	Alcoholic Liver Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0008574	gangrene	skos:exactMatch	DOID:9001699	gangrene	semapv:ManualMappingCuration	2023-12-04
EFO:0008576	Spinal Osteochondrosis	skos:exactMatch	DOID:9008900	Spinal Osteochondrosis	semapv:ManualMappingCuration	2023-12-04
EFO:0008577	Juvenile Osteochondrosis	skos:exactMatch	DOID:8125	osteochondrosis	semapv:ManualMappingCuration	2023-12-04
EFO:0008581	salivary gland disease	skos:exactMatch	DOID:10854	salivary gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:0008583	acute myocardial infarction	skos:exactMatch	DOID:9408	acute myocardial infarction	semapv:ManualMappingCuration	2022-01-24
EFO:0008585	ST Elevation Myocardial Infarction	skos:exactMatch	DOID:9000740	ST Elevation Myocardial Infarction	semapv:ManualMappingCuration	2023-12-04
EFO:0008586	Non-ST Elevation Myocardial Infarction	skos:exactMatch	DOID:9004391	Non-ST Elevated Myocardial Infarction	semapv:ManualMappingCuration	2023-12-04
EFO:0008587	gender identity disorder	skos:exactMatch	DOID:1234	gender incongruence	semapv:ManualMappingCuration	2022-01-24
EFO:0008588	peritonitis	skos:exactMatch	DOID:8283	peritonitis	semapv:ManualMappingCuration	2022-01-24
EFO:0008590	Status Asthmaticus	skos:exactMatch	DOID:9362	status asthmaticus	semapv:ManualMappingCuration	2022-01-24
EFO:0008597	anti-p200 pemphigoid	skos:exactMatch	DOID:8506	bullous pemphigoid	semapv:ManualMappingCuration	2023-12-04
EFO:0008598	autoimmune bullous skin disease	skos:exactMatch	DOID:8502	bullous skin disease	semapv:ManualMappingCuration	2022-01-24
EFO:0008598	autoimmune bullous skin disease	skos:exactMatch	DOID:8506	bullous pemphigoid	semapv:ManualMappingCuration	2023-12-04
EFO:0008601	pemphigus foliaceus	skos:exactMatch	DOID:0080850	pemphigus foliaceus	semapv:ManualMappingCuration	2023-03-17
EFO:0008602	paraneoplastic pemphigus	skos:exactMatch	DOID:0080852	paraneoplastic pemphigus	semapv:ManualMappingCuration	2023-03-17
EFO:0008603	pemphigus erythematosus	skos:exactMatch	DOID:9004056	pemphigus erythematosus	semapv:ManualMappingCuration	2023-12-04
EFO:0008604	IgA pemphigus	skos:exactMatch	DOID:0080851	IgA pemphigus	semapv:ManualMappingCuration	2023-12-04
EFO:0008605	IgG/IgA pemphigus	skos:exactMatch	DOID:9182	pemphigus	semapv:ManualMappingCuration	2023-12-04
EFO:0008606	pemphigus herpetiformis	skos:exactMatch	DOID:9001165	pemphigus herpetiformis	semapv:ManualMappingCuration	2023-12-04
EFO:0008607	drug-induced pemphigus	skos:exactMatch	DOID:9182	pemphigus	semapv:ManualMappingCuration	2023-12-04
EFO:0008608	radiotherapy-induced pemphigus	skos:exactMatch	DOID:9182	pemphigus	semapv:ManualMappingCuration	2023-12-04
EFO:0008610	ocular cicatricial pemphigoid	skos:exactMatch	DOID:11656	cicatricial pemphigoid	semapv:ManualMappingCuration	2023-12-04
EFO:0008611	localised cicatricial pemphigoid	skos:exactMatch	DOID:11656	cicatricial pemphigoid	semapv:ManualMappingCuration	2023-12-04
EFO:0008612	vegetating cicatricial pemphigoid	skos:exactMatch	DOID:11656	cicatricial pemphigoid	semapv:ManualMappingCuration	2023-12-04
EFO:0008613	pemphigus vegetans	skos:exactMatch	DOID:9006491	pemphigus vegetans	semapv:ManualMappingCuration	2023-12-04
EFO:0008614	Iodine Deficiency Hypothyroidism	skos:exactMatch	DOID:5083	iodine hypothyroidism	semapv:ManualMappingCuration	2023-12-04
EFO:0008615	Cystic Kidney Disease	skos:exactMatch	DOID:2975	cystic kidney disease	semapv:ManualMappingCuration	2022-01-24
EFO:0008616	Complex Cyst of Kidney	skos:exactMatch	DOID:2975	cystic kidney disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008618	Medullary Cystic Kidney Disease Type II	skos:exactMatch	DOID:9007051	Autosomal Dominant Tubulointerstitial Kidney Disease 1	semapv:ManualMappingCuration	2023-12-04
EFO:0008619	Simple Cyst of Kidney	skos:exactMatch	DOID:2975	cystic kidney disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008620	Polycystic Kidney Disease	skos:exactMatch	DOID:0080322	polycystic kidney disease	semapv:ManualMappingCuration	2023-03-06
EFO:0008621	Microcystic Renal Disease	skos:exactMatch	DOID:0080322	polycystic kidney disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008622	female genital tract polyp	skos:exactMatch	DOID:229	female reproductive system disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008623	dysthymic disorder	skos:exactMatch	DOID:12139	dysthymic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0008624	vitreous body disease	skos:exactMatch	DOID:9720	vitreous disease	semapv:ManualMappingCuration	2023-12-04
EFO:0008625	vitreous prolapse	skos:exactMatch	DOID:9000818	vitreous prolapse	semapv:ManualMappingCuration	2023-12-04
EFO:0008626	vitreous hemorrhage	skos:exactMatch	DOID:9007302	Vitreous Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0008627	eye hemorrhage	skos:exactMatch	DOID:9004938	Eye Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0008997	synovitis	skos:exactMatch	DOID:2703	synovitis	semapv:ManualMappingCuration	2022-01-24
EFO:0008998	acute synovitis	skos:exactMatch	DOID:9003670	acute synovitis	semapv:ManualMappingCuration	2023-12-04
EFO:0009000	Mast Cell Neoplasm	skos:exactMatch	DOID:3664	mast cell neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0009001	Mastocytosis	skos:exactMatch	DOID:350	mastocytosis	semapv:ManualMappingCuration	2022-01-24
EFO:0009002	splenic disease	skos:exactMatch	DOID:2529	splenic disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009003	ovarian dysfunction	skos:exactMatch	DOID:1414	ovarian dysfunction	semapv:ManualMappingCuration	2022-01-24
EFO:0009004	hyperestrogenism	skos:exactMatch	DOID:14336	estrogen excess	semapv:ManualMappingCuration	2022-01-24
EFO:0009005	premature menopause	skos:exactMatch	DOID:10787	premature menopause	semapv:ManualMappingCuration	2022-01-24
EFO:0009006	hyperandrogenism	skos:exactMatch	DOID:11613	hyperandrogenism	semapv:ManualMappingCuration	2023-12-04
EFO:0009007	Adrenal Hyperandrogenism	skos:exactMatch	DOID:0090139	cortisone reductase deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0009008	Ovarian Hyperandrogenism	skos:exactMatch	DOID:9006146	Ovarian Hyperandrogenism	semapv:ManualMappingCuration	2023-12-04
EFO:0009009	Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome	skos:exactMatch	DOID:8553	pyoderma gangrenosum	semapv:ManualMappingCuration	2023-12-04
EFO:0009011	Arteritis	skos:exactMatch	DOID:9002564	Arteritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009012	Polyarteritis Nodosa	skos:exactMatch	DOID:9810	polyarteritis nodosa	semapv:ManualMappingCuration	2022-01-24
EFO:0009014	3-methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia	skos:exactMatch	DOID:0110003	3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia	semapv:ManualMappingCuration	2022-01-24
EFO:0009015	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome	skos:exactMatch	DOID:0070055	Xia-Gibbs syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009016	Ataxia-oculomotor apraxia type 4	skos:exactMatch	DOID:0081383	ataxia-oculomotor apraxia type 4	semapv:ManualMappingCuration	2023-12-04
EFO:0009017	Autosomal recessive spastic paraplegia type 57	skos:exactMatch	DOID:0110809	hereditary spastic paraplegia 57	semapv:ManualMappingCuration	2023-12-04
EFO:0009018	Autosomal recessive spastic paraplegia type 75	skos:exactMatch	DOID:0110820	hereditary spastic paraplegia 75	semapv:ManualMappingCuration	2023-12-04
EFO:0009019	Autosomal recessive spastic paraplegia type 76	skos:exactMatch	DOID:0110821	hereditary spastic paraplegia 76	semapv:ManualMappingCuration	2023-12-04
EFO:0009020	Aymé-Gripp syndrome	skos:exactMatch	DOID:0111688	Ayme-Gripp syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009021	Bardet-Biedl syndrome 1	skos:exactMatch	DOID:0110123	Bardet-Biedl syndrome 1	semapv:ManualMappingCuration	2023-12-04
EFO:0009022	Bardet-Biedl syndrome 10	skos:exactMatch	DOID:0110132	Bardet-Biedl syndrome 10	semapv:ManualMappingCuration	2023-12-04
EFO:0009023	Bardet-Biedl syndrome 12	skos:exactMatch	DOID:0110134	Bardet-Biedl syndrome 12	semapv:ManualMappingCuration	2023-12-04
EFO:0009024	Bardet-Biedl syndrome 4	skos:exactMatch	DOID:0110126	Bardet-Biedl syndrome 4	semapv:ManualMappingCuration	2023-12-04
EFO:0009025	Bardet-Biedl syndrome 5	skos:exactMatch	DOID:0110127	Bardet-Biedl syndrome 5	semapv:ManualMappingCuration	2023-12-04
EFO:0009026	Bardet-Biedl syndrome 7	skos:exactMatch	DOID:0110129	Bardet-Biedl syndrome 7	semapv:ManualMappingCuration	2023-12-04
EFO:0009027	Bardet-Biedl syndrome 9	skos:exactMatch	DOID:0110131	Bardet-Biedl syndrome 9	semapv:ManualMappingCuration	2023-12-04
EFO:0009028	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome	skos:exactMatch	DOID:0090127	camptodactyly-arthropathy-coxa vara-pericarditis syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0009029	Central precocious puberty	skos:exactMatch	DOID:0112308	central precocious puberty	semapv:ManualMappingCuration	2023-03-17
EFO:0009030	Cerebellar-facial-dental syndrome	skos:exactMatch	DOID:0080898	cerebellofaciodental syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009031	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome	skos:exactMatch	DOID:9006799	CHOPS Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009032	Combined oxidative phosphorylation defect type 21	skos:exactMatch	DOID:0111465	combined oxidative phosphorylation deficiency 21	semapv:ManualMappingCuration	2023-12-04
EFO:0009033	Combined oxidative phosphorylation defect type 23	skos:exactMatch	DOID:0111500	combined oxidative phosphorylation deficiency 23	semapv:ManualMappingCuration	2023-12-04
EFO:0009034	Combined oxidative phosphorylation defect type 24	skos:exactMatch	DOID:0111485	combined oxidative phosphorylation deficiency 24	semapv:ManualMappingCuration	2023-12-04
EFO:0009035	Combined oxidative phosphorylation defect type 25	skos:exactMatch	DOID:0111468	combined oxidative phosphorylation deficiency 25	semapv:ManualMappingCuration	2023-12-04
EFO:0009036	Combined oxidative phosphorylation defect type 26	skos:exactMatch	DOID:0111490	combined oxidative phosphorylation deficiency 26	semapv:ManualMappingCuration	2023-12-04
EFO:0009037	Combined oxidative phosphorylation defect type 27	skos:exactMatch	DOID:0111489	combined oxidative phosphorylation deficiency 27	semapv:ManualMappingCuration	2023-12-04
EFO:0009038	Combined oxidative phosphorylation defect type 30	skos:exactMatch	DOID:0111471	combined oxidative phosphorylation deficiency 30	semapv:ManualMappingCuration	2023-12-04
EFO:0009039	Congenital bile acid synthesis defect	skos:exactMatch	DOID:0050674	congenital bile acid synthesis defect	semapv:ManualMappingCuration	2022-01-24
EFO:0009040	Cranio-cervical dystonia with laryngeal and upper-limb involvement	skos:exactMatch	DOID:0090052	dystonia 24	semapv:ManualMappingCuration	2023-12-04
EFO:0009041	Cushing syndrome due to macronodular adrenal hyperplasia	skos:exactMatch	DOID:0111622	ACTH-independent macronodular adrenal hyperplasia	semapv:ManualMappingCuration	2023-11-19
EFO:0009042	Estrogen resistance syndrome	skos:exactMatch	DOID:9002239	Estrogen Resistance	semapv:ManualMappingCuration	2023-12-04
EFO:0009043	Familial porphyria cutanea tarda	skos:exactMatch	DOID:3132	porphyria cutanea tarda	semapv:ManualMappingCuration	2023-12-04
EFO:0009044	Fanconi anemia complementation group A	skos:exactMatch	DOID:0111095	Fanconi anemia complementation group A	semapv:ManualMappingCuration	2023-12-04
EFO:0009045	Fanconi anemia complementation group F	skos:exactMatch	DOID:0111088	Fanconi anemia complementation group F	semapv:ManualMappingCuration	2023-12-04
EFO:0009046	Fanconi anemia complementation group G	skos:exactMatch	DOID:0111086	Fanconi anemia complementation group G	semapv:ManualMappingCuration	2023-12-04
EFO:0009048	Intrahepatic cholestasis of pregnancy	skos:exactMatch	DOID:0070227	intrahepatic cholestasis of pregnancy	semapv:ManualMappingCuration	2023-12-04
EFO:0009049	Juvenile nephropathic cystinosis	skos:exactMatch	DOID:9002714	Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type	semapv:ManualMappingCuration	2023-12-04
EFO:0009050	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome	skos:exactMatch	DOID:9004356	Smith-Kingsmore Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009051	Non-immune hydrops fetalis	skos:exactMatch	DOID:9008386	Hydrops Fetalis	semapv:ManualMappingCuration	2023-12-04
EFO:0009052	Pleuropulmonary blastoma	skos:exactMatch	DOID:4769	pleuropulmonary blastoma	semapv:ManualMappingCuration	2023-03-06
EFO:0009053	Primary progressive aphasia	skos:exactMatch	DOID:0081388	primary progressive aphasia	semapv:ManualMappingCuration	2023-12-04
EFO:0009054	Pulmonary arterial hypertension associated with congenital heart disease	skos:exactMatch	DOID:9001820	Pulmonary Arterial Hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0009055	RIDDLE syndrome	skos:exactMatch	DOID:0090113	Riddle syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009056	Spinocerebellar ataxia type 38	skos:exactMatch	DOID:0050985	spinocerebellar ataxia type 38	semapv:ManualMappingCuration	2023-12-04
EFO:0009057	Spinocerebellar ataxia type 40	skos:exactMatch	DOID:0050986	spinocerebellar ataxia type 40	semapv:ManualMappingCuration	2023-12-04
EFO:0009058	Spinocerebellar ataxia type 41	skos:exactMatch	DOID:0111744	cerebellar ataxia type 41	semapv:ManualMappingCuration	2023-12-04
EFO:0009059	Spinocerebellar ataxia type 42	skos:exactMatch	DOID:0111742	cerebellar ataxia type 42	semapv:ManualMappingCuration	2023-03-06
EFO:0009060	Spinocerebellar ataxia type 43	skos:exactMatch	DOID:0111745	cerebellar ataxia type 43	semapv:ManualMappingCuration	2023-12-04
EFO:0009061	TELO2-related intellectual disability-neurodevelopmental disorder	skos:exactMatch	DOID:9008826	YOU-HOOVER-FONG SYNDROME	semapv:ManualMappingCuration	2023-12-04
EFO:0009062	Temple-Baraitser syndrome	skos:exactMatch	DOID:9007410	Temple-Baraitser syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009063	Wolfram-like syndrome	skos:exactMatch	DOID:0080584	autosomal dominant Wolfram syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009064	X-linked erythropoietic protoporphyria	skos:exactMatch	DOID:9008396	Erythropoietic Protoporphyria, X-Linked Dominant	semapv:ManualMappingCuration	2023-12-04
EFO:0009065	calcium oxalate urolithiasis	skos:exactMatch	DOID:0080652	calcium oxalate nephrolithiasis	semapv:ManualMappingCuration	2023-12-04
EFO:0009066	clcn4-related disorder	skos:exactMatch	DOID:0112060	Raynaud-Claes syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009067	combined partial 17-alpha-hydroxylase/17,20-lyase deficiency	skos:exactMatch	DOID:9000172	17,20-Lyase Deficiency, Isolated	semapv:ManualMappingCuration	2023-12-04
EFO:0009069	hepatic methionine adenosyltransferase deficiency	skos:exactMatch	DOID:0050544	hypermethioninemia	semapv:ManualMappingCuration	2023-12-04
EFO:0009070	intellectual developmental disorder with dysmorphic facies and ptosis	skos:exactMatch	DOID:9008892	Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009071	malignant hyperthermia, susceptibility to, 1	skos:exactMatch	DOID:0080990	King Denborough syndrome	semapv:ManualMappingCuration	2024-04-21
EFO:0009072	mbd5 associated neurodevelopmental disorder	skos:exactMatch	DOID:0070031	autosomal dominant intellectual developmental disorder 1	semapv:ManualMappingCuration	2023-12-04
EFO:0009073	methylmalonic aciduria (cobalamin deficiency) cblA type	skos:exactMatch	DOID:0060742	methylmalonic acidemia cblA type	semapv:ManualMappingCuration	2023-12-04
EFO:0009074	methylmalonic aciduria cblb type	skos:exactMatch	DOID:0060743	methylmalonic acidemia cblB type	semapv:ManualMappingCuration	2023-12-04
EFO:0009075	neuropathy, hereditary motor and sensory, type vib	skos:exactMatch	DOID:9008547	Charcot-Marie-Tooth Disease Type 6B	semapv:ManualMappingCuration	2023-12-04
EFO:0009076	nonsyndromic deafness	skos:exactMatch	DOID:0050563	nonsyndromic deafness	semapv:ManualMappingCuration	2022-01-24
EFO:0009077	premature chromatid separation trait	skos:exactMatch	DOID:9007183	Premature Chromatid Separation Trait	semapv:ManualMappingCuration	2023-12-04
EFO:0009078	stag1-related disorder	skos:exactMatch	DOID:0080238	autosomal dominant intellectual developmental disorder 47	semapv:ManualMappingCuration	2023-12-04
EFO:0009079	white-sutton syndrome	skos:exactMatch	DOID:0070067	White-Sutton syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0009080	x-linked ichthyosis with steryl-sulfatase deficiency	skos:exactMatch	DOID:1700	X-linked ichthyosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009081	Heterotaxia	skos:exactMatch	DOID:0050545	visceral heterotaxy	semapv:ManualMappingCuration	2023-12-04
EFO:0009082	Pilomatrixoma	skos:exactMatch	DOID:5374	pilomatrixoma	semapv:ManualMappingCuration	2022-01-24
EFO:0009084	Endarteritis	skos:exactMatch	DOID:9001236	Endarteritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009085	arterial occlusive disease	skos:exactMatch	DOID:9006474	Arterial Occlusive Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0009086	arteriosclerosis	skos:exactMatch	DOID:2349	arteriosclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:0009087	non-typhoidal Salmonella bacteremia	skos:exactMatch	DOID:9005036	Bacteremia	semapv:ManualMappingCuration	2023-12-04
EFO:0009093	choroidal melanoma	skos:exactMatch	DOID:6438	malignant choroid melanoma	semapv:ManualMappingCuration	2023-12-04
EFO:0009094	idiopathic dilated cardiomyopathy	skos:exactMatch	DOID:12930	dilated cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009104	hyperuricemia	skos:exactMatch	DOID:1920	hyperuricemia	semapv:ManualMappingCuration	2023-12-04
EFO:0009117	typhus	skos:exactMatch	DOID:11256	typhus	semapv:ManualMappingCuration	2022-01-24
EFO:0009118	female reproductive endometrioid cancer	skos:exactMatch	DOID:3001	female reproductive endometrioid cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0009119	precursor lymphoblastic lymphoma/leukemia	skos:exactMatch	DOID:9952	acute lymphoblastic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:0009135	leigh syndrome due to mitochondrial complex iv deficiency	skos:exactMatch	DOID:9000658	Leigh Syndrome due to Mitochondrial Complex IV Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0009136	heterotaxy, visceral, x-linked	skos:exactMatch	DOID:9003587	Congenital Heart Defects, Multiple Types, 1, X-Linked	semapv:ManualMappingCuration	2023-12-04
EFO:0009137	renal hypodysplasia/aplasia 3	skos:exactMatch	DOID:9009100	Renal Hypodysplasia/Aplasia 3	semapv:ManualMappingCuration	2023-12-04
EFO:0009138	laminin alpha 2-related dystrophy	skos:exactMatch	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A	semapv:ManualMappingCuration	2023-12-04
EFO:0009139	glut1 deficiency syndrome 1, autosomal recessive	skos:exactMatch	DOID:0070561	glucose transporter type 1 deficiency syndrome 1	semapv:ManualMappingCuration	2024-08-10
EFO:0009139	glut1 deficiency syndrome 1, autosomal recessive	skos:exactMatch	DOID:9007802	GLUT1 Deficiency Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009140	metastatic pancreatic neuroendocrine tumours	skos:exactMatch	DOID:1798	pancreatic endocrine carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0009141	fgfr2 related craniosynostosis	skos:exactMatch	DOID:2340	craniosynostosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009142	autosomal dominant dilated cardiomyopathy	skos:exactMatch	DOID:12930	dilated cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009144	Lethal neonatal spasticity-epileptic encephalopathy syndrome	skos:exactMatch	DOID:9003268	Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal	semapv:ManualMappingCuration	2023-12-04
EFO:0009145	limb-girdle muscular dystrophy-dystroglycanopathy, type c1	skos:exactMatch	DOID:0110297	autosomal recessive limb-girdle muscular dystrophy type 2K	semapv:ManualMappingCuration	2023-12-04
EFO:0009146	pik3ca related overgrowth spectrum	skos:exactMatch	DOID:9002647	Megalencephaly - Cutis Marmorata Telangiectatica Congenita	semapv:ManualMappingCuration	2023-12-04
EFO:0009147	partial adenosine deaminase deficiency	skos:exactMatch	DOID:5810	adenosine deaminase deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0009148	acth-independent macronodular adrenal hyperplasia 2	skos:exactMatch	DOID:0111624	ACTH-independent macronodular adrenal hyperplasia 2	semapv:ManualMappingCuration	2023-12-04
EFO:0009149	muscular dystrophy, congenital, with cataracts and intellectual disability	skos:exactMatch	DOID:0080197	congenital muscular dystrophy with cataracts and intellectual disability	semapv:ManualMappingCuration	2022-01-24
EFO:0009150	cholestasis, intrahepatic, of pregnancy 3	skos:exactMatch	DOID:0070229	intrahepatic cholestasis of pregnancy 3	semapv:ManualMappingCuration	2023-12-04
EFO:0009151	cone-rod dystrophy and hearing loss	skos:exactMatch	DOID:9000732	Cone-Rod Dystrophy and Hearing Loss	semapv:ManualMappingCuration	2023-12-04
EFO:0009152	intellectual disability, autosomal dominant 52	skos:exactMatch	DOID:0080231	autosomal dominant intellectual developmental disorder 52	semapv:ManualMappingCuration	2022-01-24
EFO:0009153	lymphedema, hereditary, iii	skos:exactMatch	DOID:9000957	lymphatic malformation 6	semapv:ManualMappingCuration	2023-12-04
EFO:0009154	hemophilia b leyden	skos:exactMatch	DOID:12259	hemophilia B	semapv:ManualMappingCuration	2023-12-04
EFO:0009155	growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy	skos:exactMatch	DOID:9002230	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY	semapv:ManualMappingCuration	2023-12-04
EFO:0009156	intellectual disability, autosomal dominant 48	skos:exactMatch	DOID:0080235	autosomal dominant intellectual developmental disorder 48	semapv:ManualMappingCuration	2022-01-24
EFO:0009157	susceptibility to malaria	skos:exactMatch	DOID:12365	malaria	semapv:ManualMappingCuration	2023-12-04
EFO:0009158	encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy	skos:exactMatch	DOID:9006901	Early-Onset Progressive Encephalopathy with Brain Edema and/or Leukoencephalopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009159	combined oxidative phosphorylation deficiency 33	skos:exactMatch	DOID:0111495	combined oxidative phosphorylation deficiency 33	semapv:ManualMappingCuration	2023-12-04
EFO:0009160	stromme syndrome	skos:exactMatch	DOID:0110595	Stromme syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0009161	debrisoquine, poor metabolism of	skos:exactMatch	DOID:9002295	Poor Drug Metabolism, CYP2D6-Related	semapv:ManualMappingCuration	2023-12-04
EFO:0009162	charcot-marie-tooth disease, axonal, type 2t	skos:exactMatch	DOID:0110160	Charcot-Marie-Tooth disease axonal type 2T	semapv:ManualMappingCuration	2022-01-24
EFO:0009163	woolly hair, autosomal recessive 2, with or without hypotrichosis	skos:exactMatch	DOID:0110704	hypotrichosis 7	semapv:ManualMappingCuration	2023-12-04
EFO:0009164	intellectual disability, autosomal dominant 54	skos:exactMatch	DOID:0080230	autosomal dominant intellectual developmental disorder 54	semapv:ManualMappingCuration	2022-01-24
EFO:0009165	intellectual disability, autosomal dominant 53	skos:exactMatch	DOID:0080228	autosomal dominant intellectual developmental disorder 53	semapv:ManualMappingCuration	2022-01-24
EFO:0009189	hyperthyroidism	skos:exactMatch	DOID:7998	hyperthyroidism	semapv:ManualMappingCuration	2022-01-24
EFO:0009190	Thyrotoxicosis	skos:exactMatch	DOID:7997	thyrotoxicosis	semapv:ManualMappingCuration	2022-01-24
EFO:0009191	Toxic Nodular Goiter	skos:exactMatch	DOID:11277	Plummer's disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009192	Drug- or toxin-induced pulmonary arterial hypertension	skos:exactMatch	DOID:9001820	Pulmonary Arterial Hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0009194	Pulmonary arterial hypertension associated with HIV infection	skos:exactMatch	DOID:9001820	Pulmonary Arterial Hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0009195	Pulmonary arterial hypertension associated with chronic hemolytic anemia	skos:exactMatch	DOID:9001820	Pulmonary Arterial Hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0009197	Pulmonary arterial hypertension associated with portal hypertension	skos:exactMatch	DOID:9001820	Pulmonary Arterial Hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0009198	Pulmonary arterial hypertension associated with schistosomiasis	skos:exactMatch	DOID:9001820	Pulmonary Arterial Hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0009200	Eisenmenger syndrome	skos:exactMatch	DOID:9004363	Eisenmenger Complex	semapv:ManualMappingCuration	2023-12-04
EFO:0009201	myopic macular degeneration	skos:exactMatch	DOID:4448	macular degeneration	semapv:ManualMappingCuration	2023-12-04
EFO:0009254	optic nerve glioblastoma	skos:exactMatch	DOID:4992	optic nerve glioma	semapv:ManualMappingCuration	2022-01-24
EFO:0009255	cecal neoplasm	skos:exactMatch	DOID:1517	cecal benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:0009255	cecal neoplasm	skos:exactMatch	DOID:9003694	Cecal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:0009259	skin carcinoma	skos:exactMatch	DOID:3451	skin carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:0009260	non-melanoma skin carcinoma	skos:exactMatch	DOID:3451	skin carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0009266	refractory celiac disease	skos:exactMatch	DOID:9002592	refractory celiac disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009267	delirium	skos:exactMatch	DOID:8645	subacute delirium	semapv:ManualMappingCuration	2023-12-04
EFO:0009275	premature cardiac contractions	skos:exactMatch	DOID:9002737	Premature Cardiac Complexes	semapv:ManualMappingCuration	2023-12-04
EFO:0009276	ventricular ectopy	skos:exactMatch	DOID:9007033	Ventricular Premature Complexes	semapv:ManualMappingCuration	2023-12-04
EFO:0009277	supraventricular ectopy	skos:exactMatch	DOID:9000514	Atrial Premature Complexes	semapv:ManualMappingCuration	2023-12-04
EFO:0009295	polyarteritis nodosa, childhoood-onset	skos:exactMatch	DOID:9008412	Polyarteritis Nodosa, Childhood-Onset	semapv:ManualMappingCuration	2023-12-04
EFO:0009296	mutyh-associated polyposis	skos:exactMatch	DOID:0080410	familial adenomatous polyposis 2	semapv:ManualMappingCuration	2023-12-04
EFO:0009297	fg syndrome	skos:exactMatch	DOID:14711	FG syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0009298	hepatic failure, early-onset, and neurologic disorder due to cytochrome c oxidase deficiency	skos:exactMatch	DOID:3762	cytochrome-c oxidase deficiency disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009299	marfan syndrome/loeys-dietz syndrome/familial thoracic aortic aneurysms and dissections	skos:exactMatch	DOID:0070234	Loeys-Dietz syndrome 2	semapv:ManualMappingCuration	2023-12-04
EFO:0009300	neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant	skos:exactMatch	DOID:0070038	autosomal dominant intellectual developmental disorder 8	semapv:ManualMappingCuration	2023-12-04
EFO:0009301	dystonia 28, childhood-onset	skos:exactMatch	DOID:0060936	dystonia 28, childhood-onset	semapv:ManualMappingCuration	2024-05-19
EFO:0009301	dystonia 28, childhood-onset	skos:exactMatch	DOID:9004049	Dystonia 28, Childhood-onset	semapv:ManualMappingCuration	2023-12-04
EFO:0009302	amelogenesis imperfecta, type ij	skos:exactMatch	DOID:0080953	amelogenesis imperfecta type 1J	semapv:ManualMappingCuration	2023-04-17
EFO:0009313	Linear IgA Dermatosis	skos:exactMatch	DOID:9005191	Linear IgA Bullous Dermatosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009314	blood coagulation disease	skos:exactMatch	DOID:1247	blood coagulation disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009315	thrombophilia	skos:exactMatch	DOID:2452	thrombophilia	semapv:ManualMappingCuration	2022-01-24
EFO:0009316	protein c deficiency	skos:exactMatch	DOID:3756	protein C deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0009321	diabetic macular edema	skos:exactMatch	DOID:9191	diabetic macular edema	semapv:ManualMappingCuration	2022-01-24
EFO:0009322	proliferative diabetic retinopathy	skos:exactMatch	DOID:13207	proliferative diabetic retinopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0009339	Herpes simplex virus 2 seropositivity	skos:exactMatch	DOID:8566	herpes simplex	semapv:ManualMappingCuration	2023-12-04
EFO:0009361	colorectal mucinous adenocarcinoma	skos:exactMatch	DOID:0050861	colorectal adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0009363	chronic central serous retinopathy	skos:exactMatch	DOID:9003248	Central Serous Chorioretinopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009365	vaginal discharge	skos:exactMatch	DOID:3767	vaginal discharge	semapv:ManualMappingCuration	2023-12-04
EFO:0009373	edema	skos:exactMatch	DOID:9000197	Edema	semapv:ManualMappingCuration	2023-12-04
EFO:0009380	facial neuralgia	skos:exactMatch	DOID:13865	facial neuralgia	semapv:ManualMappingCuration	2022-01-24
EFO:0009382	metabolically healthy obesity	skos:exactMatch	DOID:9006237	Metabolically Benign Obesity	semapv:ManualMappingCuration	2023-12-04
EFO:0009383	tumoral calcinosis, hyperphosphatemic, familial, 2	skos:exactMatch	DOID:9007069	Hyperphosphatemic Familial Tumoral Calcinosis 2	semapv:ManualMappingCuration	2023-12-04
EFO:0009384	tumoral calcinosis, hyperphosphatemic, familial, 3	skos:exactMatch	DOID:9005366	Hyperphosphatemic Familial Tumoral Calcinosis 3	semapv:ManualMappingCuration	2023-12-04
EFO:0009385	familial tumoral calcinosis	skos:exactMatch	DOID:0111063	hyperphosphatemic familial tumoral calcinosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009385	familial tumoral calcinosis	skos:exactMatch	DOID:9007993	Dehydration	semapv:ManualMappingCuration	2023-12-04
EFO:0009386	central nervous system disease	skos:exactMatch	DOID:331	central nervous system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009387	peripheral nervous system disease	skos:exactMatch	DOID:574	peripheral nervous system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009406	glucose metabolism disease	skos:exactMatch	DOID:4194	glucose metabolism disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009424	Yersinia enterocolitica infectious disease	skos:exactMatch	DOID:9000171	Yersinia enterocolitica infections	semapv:ManualMappingCuration	2023-12-04
EFO:0009425	Yersinia pestis infectious disease	skos:exactMatch	DOID:3482	plague	semapv:ManualMappingCuration	2022-01-24
EFO:0009426	necrosis	skos:exactMatch	DOID:9005749	Necrosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009429	Mycobacterium infection	skos:exactMatch	DOID:9001415	Mycobacterium Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0009430	neuralgia	skos:exactMatch	DOID:9005968	Neuralgia	semapv:ManualMappingCuration	2023-12-04
EFO:0009431	intestinal disease	skos:exactMatch	DOID:5295	intestinal disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009432	fibroblastic disorder	skos:exactMatch	DOID:65	connective tissue disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009433	lower respiratory tract disease	skos:exactMatch	DOID:0050161	lower respiratory tract disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009434	death by undetermined cause	skos:exactMatch	DOID:9000543	Death	semapv:ManualMappingCuration	2023-12-04
EFO:0009441	Waldenstrom macroglobulinemia	skos:exactMatch	DOID:0060901	lymphoplasmacytic lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:0009443	BRCAX breast cancer	skos:exactMatch	DOID:9006047	Breast Cancer 3	semapv:ManualMappingCuration	2023-12-04
EFO:0009444	hypoxia	skos:exactMatch	DOID:9002669	Hypoxia	semapv:ManualMappingCuration	2023-12-04
EFO:0009446	asphyxia	skos:exactMatch	DOID:9001041	Asphyxia	semapv:ManualMappingCuration	2023-12-04
EFO:0009448	pulmonary fibrosis	skos:exactMatch	DOID:3770	pulmonary fibrosis	semapv:ManualMappingCuration	2022-01-24
EFO:0009449	keratitis	skos:exactMatch	DOID:4677	keratitis	semapv:ManualMappingCuration	2022-01-24
EFO:0009450	conjunctivitis	skos:exactMatch	DOID:6195	conjunctivitis	semapv:ManualMappingCuration	2022-01-24
EFO:0009451	hypoparathyroidism	skos:exactMatch	DOID:11199	hypoparathyroidism	semapv:ManualMappingCuration	2022-01-24
EFO:0009452	hyperaldosteronism	skos:exactMatch	DOID:446	primary hyperaldosteronism	semapv:ManualMappingCuration	2022-01-24
EFO:0009453	hemiplegia	skos:exactMatch	DOID:10969	hemiplegia	semapv:ManualMappingCuration	2022-01-24
EFO:0009454	gastric ulcer	skos:exactMatch	DOID:10808	gastric ulcer	semapv:ManualMappingCuration	2022-01-24
EFO:0009455	lacrimal apparatus disease	skos:exactMatch	DOID:1400	lacrimal apparatus disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009456	exfoliative dermatitis	skos:exactMatch	DOID:9006215	Exfoliative Dermatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0009459	ACPA-positive rheumatoid arthritis	skos:exactMatch	DOID:7148	rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009460	ACPA-negative rheumatoid arthritis	skos:exactMatch	DOID:7148	rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009463	infarction	skos:exactMatch	DOID:9005600	Infarction	semapv:ManualMappingCuration	2023-12-04
EFO:0009464	corneal disease	skos:exactMatch	DOID:10124	corneal disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009466	Löfgren’s syndrome	skos:exactMatch	DOID:9006296	Lofgren’s syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009468	jaw disease	skos:exactMatch	DOID:9003876	Jaw Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0009469	Bartholin gland disease	skos:exactMatch	DOID:60002	Bartholin's gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009470	soft tissue disease	skos:exactMatch	DOID:9005306	soft tissue disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009471	small kidney	skos:exactMatch	DOID:0080204	renal hypoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0009472	tympanic membrane perforation	skos:exactMatch	DOID:9004210	Tympanic Membrane Perforation	semapv:ManualMappingCuration	2023-12-04
EFO:0009473	hemolysis	skos:exactMatch	DOID:9003603	Hemolysis	semapv:ManualMappingCuration	2023-12-04
EFO:0009475	cervical polyp	skos:exactMatch	DOID:0060325	cervical polyp	semapv:ManualMappingCuration	2023-12-04
EFO:0009476	neck injury	skos:exactMatch	DOID:9002927	Neck Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009477	vertebral joint disease	skos:exactMatch	DOID:381	arthropathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009478	vocal cord polyp	skos:exactMatch	DOID:9003896	Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:0009479	throat disease	skos:exactMatch	DOID:9007241	Otorhinolaryngologic Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0009481	paranasal sinus disease	skos:exactMatch	DOID:1352	paranasal sinus disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009482	drug allergy	skos:exactMatch	DOID:0060500	drug allergy	semapv:ManualMappingCuration	2022-01-24
EFO:0009483	breast disease	skos:exactMatch	DOID:3463	breast disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009484	uterine polyp	skos:exactMatch	DOID:9042	polyp of corpus uteri	semapv:ManualMappingCuration	2022-01-24
EFO:0009485	eye injury	skos:exactMatch	DOID:9006447	Eye Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009486	diabetic eye disease	skos:exactMatch	DOID:8947	diabetic retinopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009487	nerve compression syndrome	skos:exactMatch	DOID:573	nerve compression syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:0009488	spinal cord disease	skos:exactMatch	DOID:319	spinal cord disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009489	cranial nerve palsy	skos:exactMatch	DOID:3817	cranial nerve palsy	semapv:ManualMappingCuration	2022-01-24
EFO:0009490	nervous system injury	skos:exactMatch	DOID:9006062	Nervous System Trauma	semapv:ManualMappingCuration	2023-12-04
EFO:0009491	adrenocortical insufficiency	skos:exactMatch	DOID:10493	adrenal cortical hypofunction	semapv:ManualMappingCuration	2022-01-24
EFO:0009492	cardiac arrest	skos:exactMatch	DOID:0060319	cardiac arrest	semapv:ManualMappingCuration	2023-12-04
EFO:0009493	paroxysmal tachycardia	skos:exactMatch	DOID:9004669	Paroxysmal Tachycardia	semapv:ManualMappingCuration	2023-12-04
EFO:0009502	abdominal injury	skos:exactMatch	DOID:9001932	Abdominal Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009503	caustic injury	skos:exactMatch	DOID:9003730	Chemical Burns	semapv:ManualMappingCuration	2023-12-04
EFO:0009504	crush injury	skos:exactMatch	DOID:9001281	Crush Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009505	head injury	skos:exactMatch	DOID:9007621	Craniocerebral Trauma	semapv:ManualMappingCuration	2023-12-04
EFO:0009506	heart injury	skos:exactMatch	DOID:9007588	Heart Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009507	knee injury	skos:exactMatch	DOID:9008290	Knee Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009508	leg injury	skos:exactMatch	DOID:9008911	Leg Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009509	limb injury	skos:exactMatch	DOID:9000623	panic disorder with agoraphobia	semapv:ManualMappingCuration	2023-12-04
EFO:0009509	limb injury	skos:exactMatch	DOID:9004073	limb injury	semapv:ManualMappingCuration	2023-12-04
EFO:0009510	peripheral nerve injury	skos:exactMatch	DOID:9001240	Peripheral Nerve Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009513	multiple bone fractures	skos:exactMatch	DOID:9007618	Fractures, Multiple	semapv:ManualMappingCuration	2023-12-04
EFO:0009515	wrist fracture	skos:exactMatch	DOID:9001085	wrist fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009516	burn	skos:exactMatch	DOID:9007730	Burns	semapv:ManualMappingCuration	2023-12-04
EFO:0009521	dislocation	skos:exactMatch	DOID:9003279	Joint Dislocations	semapv:ManualMappingCuration	2023-12-04
EFO:0009522	disturbance of skin sensation	skos:exactMatch	DOID:37	skin disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009523	fecal incontinence	skos:exactMatch	DOID:9008184	Fecal Incontinence	semapv:ManualMappingCuration	2023-12-04
EFO:0009524	female genital tract fistula	skos:exactMatch	DOID:9002824	Vaginal Fistula	semapv:ManualMappingCuration	2023-12-04
EFO:0009525	foreign body	skos:exactMatch	DOID:9003074	Foreign Bodies	semapv:ManualMappingCuration	2023-12-04
EFO:0009526	foreign body in gastrointestinal tract	skos:exactMatch	DOID:9003074	Foreign Bodies	semapv:ManualMappingCuration	2023-12-04
EFO:0009527	frostbite	skos:exactMatch	DOID:9006668	Frostbite	semapv:ManualMappingCuration	2023-12-04
EFO:0009528	AIDS-related disease	skos:exactMatch	DOID:635	acquired immunodeficiency syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009529	anemia due to enzyme disorder	skos:exactMatch	DOID:2355	anemia	semapv:ManualMappingCuration	2023-12-04
EFO:0009530	anuria	skos:exactMatch	DOID:2983	anuria	semapv:ManualMappingCuration	2022-01-24
EFO:0009531	aortic valve disease	skos:exactMatch	DOID:62	aortic valve disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009532	autonomic nervous system disease	skos:exactMatch	DOID:11465	autonomic nervous system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009533	basal ganglia disease	skos:exactMatch	DOID:679	basal ganglia disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009534	biliary tract disease	skos:exactMatch	DOID:9741	biliary tract disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009535	binocular vision disease	skos:exactMatch	DOID:12667	binocular vision disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009536	blepharitis	skos:exactMatch	DOID:9423	blepharitis	semapv:ManualMappingCuration	2022-01-24
EFO:0009537	cervical disc degenerative disorder	skos:exactMatch	DOID:90	degenerative disc disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009538	chronic inflammatory demyelinating polyneuropathy	skos:exactMatch	DOID:5213	chronic inflammatory demyelinating polyradiculoneuropathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009539	congenital mitral malformation	skos:exactMatch	DOID:11502	mitral valve insufficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0009540	dental pulp disease	skos:exactMatch	DOID:5330	dental pulp disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009541	disease of peritoneum	skos:exactMatch	DOID:9006175	Peritoneal Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0009542	disorder of appendix	skos:exactMatch	DOID:60000	appendix disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009543	disturbances of sensation of smell and taste	skos:exactMatch	DOID:0050155	sensory system disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009544	esophageal disease	skos:exactMatch	DOID:6050	esophageal disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009545	esophageal varices	skos:exactMatch	DOID:112	esophageal varix	semapv:ManualMappingCuration	2022-01-24
EFO:0009546	eye adnexa disease	skos:exactMatch	DOID:9001010	eye adnexa disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009547	eyelid disease	skos:exactMatch	DOID:530	eyelid disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009548	fallopian tube disease	skos:exactMatch	DOID:1962	fallopian tube disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009549	female reproductive system disease	skos:exactMatch	DOID:229	female reproductive system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009550	headache disorder	skos:exactMatch	DOID:9007953	Headache Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0009551	heart valve disease	skos:exactMatch	DOID:4079	heart valve disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009552	hemorrhoid	skos:exactMatch	DOID:9746	hemorrhoid	semapv:ManualMappingCuration	2022-01-24
EFO:0009553	HIV-associated cancer	skos:exactMatch	DOID:9005562	AIDS-Related Kaposi Sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:0009554	malabsorption syndrome	skos:exactMatch	DOID:9002984	Malabsorption Syndromes	semapv:ManualMappingCuration	2023-12-04
EFO:0009555	male reproductive system disease	skos:exactMatch	DOID:48	male reproductive system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009556	mineral metabolism disease	skos:exactMatch	DOID:0050032	mineral metabolism disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009557	mitral valve disease	skos:exactMatch	DOID:61	mitral valve disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009558	mononeuropathy	skos:exactMatch	DOID:1188	mononeuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:0009559	nerve plexus disease	skos:exactMatch	DOID:3688	plexopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0009560	otitis externa	skos:exactMatch	DOID:9463	otitis externa	semapv:ManualMappingCuration	2022-01-24
EFO:0009561	parasitic intestinal disease	skos:exactMatch	DOID:9002892	Parasitic Intestinal Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0009562	polyneuropathy	skos:exactMatch	DOID:1389	polyneuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:0009563	protein energy malnutrition	skos:exactMatch	DOID:11801	protein-energy malnutrition	semapv:ManualMappingCuration	2022-01-24
EFO:0009564	pulmonary valve disease	skos:exactMatch	DOID:5749	pulmonary valve disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009566	renal tubule disease	skos:exactMatch	DOID:447	renal tubular transport disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009566	renal tubule disease	skos:exactMatch	DOID:9000111	Radiation Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009567	Spirochaetales Infections	skos:exactMatch	DOID:9002423	Spirochaetales Infections	semapv:ManualMappingCuration	2023-12-04
EFO:0009568	tricuspid valve disease	skos:exactMatch	DOID:0050826	tricuspid valve disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009569	trigeminal nerve disease	skos:exactMatch	DOID:561	trigeminal nerve disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009570	tympanic membrane disease	skos:exactMatch	DOID:5782	tympanic membrane disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009571	urinary tract obstruction	skos:exactMatch	DOID:5200	urinary tract obstruction	semapv:ManualMappingCuration	2022-01-24
EFO:0009572	uterine inflammatory disease	skos:exactMatch	DOID:13736	uterine inflammatory disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009575	mosquito-borne hemorragic fever	skos:exactMatch	DOID:9007401	Viral Hemorrhagic Fevers	semapv:ManualMappingCuration	2023-12-04
EFO:0009579	postpartum hemorrhage	skos:exactMatch	DOID:9007585	Postpartum Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0009582	sprain	skos:exactMatch	DOID:9000934	Sprains and Strains	semapv:ManualMappingCuration	2023-12-04
EFO:0009584	AQP4-IgG-positive neuromyelitis optica	skos:exactMatch	DOID:8869	neuromyelitis optica	semapv:ManualMappingCuration	2023-12-04
EFO:0009585	AQP4-IgG-negative neuromyelitis optica	skos:exactMatch	DOID:8869	neuromyelitis optica	semapv:ManualMappingCuration	2023-12-04
EFO:0009601	testicular disease	skos:exactMatch	DOID:2519	testicular disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009602	prostate disease	skos:exactMatch	DOID:47	prostate disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009604	labyrinthitis	skos:exactMatch	DOID:1468	labyrinthitis	semapv:ManualMappingCuration	2022-01-24
EFO:0009604	labyrinthitis	skos:exactMatch	DOID:3930	otitis interna	semapv:ManualMappingCuration	2022-01-24
EFO:0009605	pancreas disease	skos:exactMatch	DOID:26	pancreas disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009606	macular degeneration	skos:exactMatch	DOID:4448	macular degeneration	semapv:ManualMappingCuration	2022-01-24
EFO:0009607	pituitary gland disease	skos:exactMatch	DOID:53	pituitary gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009608	stomach disease	skos:exactMatch	DOID:76	stomach disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009609	myocarditis	skos:exactMatch	DOID:820	myocarditis	semapv:ManualMappingCuration	2022-01-24
EFO:0009610	cervical spondylosis	skos:exactMatch	DOID:2247	spondylosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009611	orbital fracture	skos:exactMatch	DOID:9001115	Orbital Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009612	jaw fracture	skos:exactMatch	DOID:9004559	Jaw Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009613	fibula fracture	skos:exactMatch	DOID:9006847	fibula fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009614	clavicle fracture	skos:exactMatch	DOID:9008076	clavicle fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009615	ankle fracture	skos:exactMatch	DOID:9006786	Ankle Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009616	finger fracture	skos:exactMatch	DOID:9008375	finger fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009617	knee fracture	skos:exactMatch	DOID:9007321	knee fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009618	foot fracture	skos:exactMatch	DOID:9002589	Bone Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009619	neuroma	skos:exactMatch	DOID:2001	neuroma	semapv:ManualMappingCuration	2022-01-24
EFO:0009620	rib fracture	skos:exactMatch	DOID:9008717	Rib Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009621	shoulder fracture	skos:exactMatch	DOID:9004624	Shoulder Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009622	fracture of pelvis	skos:exactMatch	DOID:9002589	Bone Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009623	nose injury	skos:exactMatch	DOID:9001600	Wounds and Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0009624	pulmonary alveolitis	skos:exactMatch	DOID:3082	interstitial lung disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009625	facial pain	skos:exactMatch	DOID:9003932	Facial Pain	semapv:ManualMappingCuration	2023-12-04
EFO:0009626	pyloric stenosis	skos:exactMatch	DOID:12639	pyloric stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:0009626	pyloric stenosis	skos:exactMatch	DOID:3122	gastric outlet obstruction	semapv:ManualMappingCuration	2022-01-24
EFO:0009630	convalescence	skos:exactMatch	DOID:9004390	Convalescence	semapv:ManualMappingCuration	2023-12-04
EFO:0009637	pleural effusion	skos:exactMatch	DOID:9005883	Pleural Effusion	semapv:ManualMappingCuration	2023-12-04
EFO:0009644	neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy	skos:exactMatch	DOID:9009098	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY	semapv:ManualMappingCuration	2023-12-04
EFO:0009645	neurodevelopmental disorder with or without anomalies of the brain, eye, or heart	skos:exactMatch	DOID:9004468	Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart	semapv:ManualMappingCuration	2023-12-04
EFO:0009646	macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss	skos:exactMatch	DOID:0060651	MYH-9 related disease	semapv:ManualMappingCuration	2022-07-21
EFO:0009647	epilepsy, hearing loss, and intellectual disability syndrome	skos:exactMatch	DOID:9004336	neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities	semapv:ManualMappingCuration	2023-12-04
EFO:0009649	susceptibility to breast cancer	skos:exactMatch	DOID:1612	breast cancer	semapv:ManualMappingCuration	2023-12-04
EFO:0009650	hyperproinsulinemia	skos:exactMatch	DOID:9003282	Hyperproinsulinemia	semapv:ManualMappingCuration	2023-12-04
EFO:0009651	rag2 deficiency	skos:exactMatch	DOID:0060012	recombinase activating gene 2 deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0009652	neointimal hyperplasia	skos:exactMatch	DOID:9005396	Intimal Hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0009657	acute pharyngitis	skos:exactMatch	DOID:2275	pharyngitis	semapv:ManualMappingCuration	2023-12-04
EFO:0009659	aneurysm	skos:exactMatch	DOID:9001665	Aneurysm	semapv:ManualMappingCuration	2023-12-04
EFO:0009660	anus disease	skos:exactMatch	DOID:3128	anus disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009661	bronchitis	skos:exactMatch	DOID:6132	bronchitis	semapv:ManualMappingCuration	2022-01-24
EFO:0009662	common wart	skos:exactMatch	DOID:11165	common wart	semapv:ManualMappingCuration	2022-01-24
EFO:0009663	disease of genitourinary system	skos:exactMatch	DOID:9009146	Urogenital Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0009664	disease of orbital region	skos:exactMatch	DOID:930	orbital disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009665	disorder of patella	skos:exactMatch	DOID:0080001	bone disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009666	enthesopathy	skos:exactMatch	DOID:204	enthesopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0009667	eustachian tube disease	skos:exactMatch	DOID:9739	eustachian tube disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009668	external ear disease	skos:exactMatch	DOID:379	external ear disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009669	flatulence	skos:exactMatch	DOID:9001533	Flatulence	semapv:ManualMappingCuration	2023-12-04
EFO:0009670	gingival disease	skos:exactMatch	DOID:1483	gingival disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009671	hereditary ataxia	skos:exactMatch	DOID:0050951	hereditary ataxia	semapv:ManualMappingCuration	2022-01-24
EFO:0009672	inner ear disease	skos:exactMatch	DOID:2952	inner ear disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009673	laryngeal disease	skos:exactMatch	DOID:786	laryngeal disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009674	lens disease	skos:exactMatch	DOID:110	lens disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009676	musculoskeletal system disease	skos:exactMatch	DOID:17	musculoskeletal system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009676	musculoskeletal system disease	skos:exactMatch	DOID:9005120	Pigmented Nevus	semapv:ManualMappingCuration	2023-12-04
EFO:0009677	occlusion precerebral artery	skos:exactMatch	DOID:5976	occlusion precerebral artery	semapv:ManualMappingCuration	2022-01-24
EFO:0009678	paralytic strabismus	skos:exactMatch	DOID:10863	paralytic squint	semapv:ManualMappingCuration	2022-01-24
EFO:0009679	paraplegia	skos:exactMatch	DOID:607	paraplegia	semapv:ManualMappingCuration	2022-01-24
EFO:0009680	pleural empyema	skos:exactMatch	DOID:3798	pleural empyema	semapv:ManualMappingCuration	2022-01-24
EFO:0009681	post term pregnancy	skos:exactMatch	DOID:9002082	Prolonged Pregnancy	semapv:ManualMappingCuration	2023-12-04
EFO:0009682	pregnancy disorder	skos:exactMatch	DOID:9004702	Pregnancy Complications	semapv:ManualMappingCuration	2023-12-04
EFO:0009683	puerperal disorder	skos:exactMatch	DOID:9001791	Puerperal Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0009684	quadriplegia	skos:exactMatch	DOID:12835	quadriplegia	semapv:ManualMappingCuration	2022-01-24
EFO:0009685	rectal disease	skos:exactMatch	DOID:1285	rectal disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009686	respiratory failure	skos:exactMatch	DOID:11162	respiratory failure	semapv:ManualMappingCuration	2022-01-24
EFO:0009687	somatoform disorder	skos:exactMatch	DOID:4737	somatoform disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0009688	stomatitis	skos:exactMatch	DOID:9637	stomatitis	semapv:ManualMappingCuration	2022-01-24
EFO:0009689	urethral disease	skos:exactMatch	DOID:732	urethral disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009690	urinary system disease	skos:exactMatch	DOID:18	urinary system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009691	vestibular disease	skos:exactMatch	DOID:3426	vestibular disease	semapv:ManualMappingCuration	2022-01-24
EFO:0009692	voice disorders	skos:exactMatch	DOID:9006046	Voice Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0009704	radiation-induced brain injury	skos:exactMatch	DOID:9002894	radiation-induced brain injury	semapv:ManualMappingCuration	2023-12-04
EFO:0009705	small intestine enteropathy	skos:exactMatch	DOID:5295	intestinal disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009706	latent autoimmune diabetes in adults	skos:exactMatch	DOID:0080846	latent autoimmune diabetes in adults	semapv:ManualMappingCuration	2023-12-04
EFO:0009707	fractures, ununited	skos:exactMatch	DOID:9007932	Ununited Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0009708	metastasis	skos:exactMatch	DOID:9000965	Neoplasm Metastasis	semapv:ManualMappingCuration	2023-12-04
EFO:0009709	metastatic neoplasm	skos:exactMatch	DOID:9000965	Neoplasm Metastasis	semapv:ManualMappingCuration	2023-12-04
EFO:0009710	micrometastasis	skos:exactMatch	DOID:9008726	Neoplasm Micrometastasis	semapv:ManualMappingCuration	2023-12-04
EFO:0009714	chronic disease	skos:exactMatch	DOID:9000144	Chronic Disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009715	wheezing	skos:exactMatch	DOID:9003157	Respiratory Sounds	semapv:ManualMappingCuration	2023-12-04
EFO:0009727	shortness of breath	skos:exactMatch	DOID:9000590	Dyspnea	semapv:ManualMappingCuration	2023-12-04
EFO:0009730	polyarticular juvenile idiopathic arthritis	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009731	polyarticular juvenile idiopathic arthritis, rheumatoid factor positive	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009732	enthesitis-related juvenile idiopathic arthritis	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009733	psoriasis-related juvenile idiopathic arthritis	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009734	unspecified juvenile idiopathic arthritis	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009746	extended oligoarticular juvenile idiopathic arthritis	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:0009757	idiopathic type 1 diabetes	skos:exactMatch	DOID:9744	type 1 diabetes mellitus	semapv:ManualMappingCuration	2023-12-04
EFO:0009758	fulminant type 1 diabetes	skos:exactMatch	DOID:9008637	fulminant type 1 diabetes	semapv:ManualMappingCuration	2023-12-04
EFO:0009759	Chronic Obstructive Asthma	skos:exactMatch	DOID:0080809	chronic asthma	semapv:ManualMappingCuration	2023-12-04
EFO:0009760	non-proliferative diabetic retinopathy	skos:exactMatch	DOID:13208	background diabetic retinopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009761	periprosthetic osteolysis	skos:exactMatch	DOID:9003852	periprosthetic osteolysis	semapv:ManualMappingCuration	2023-12-04
EFO:0009780	HER2 negative breast carcinoma	skos:exactMatch	DOID:0060080	Her2-receptor negative breast cancer	semapv:ManualMappingCuration	2022-07-21
EFO:0009781	progesterone-receptor negative breast cancer	skos:exactMatch	DOID:0060078	progesterone-receptor negative breast cancer	semapv:ManualMappingCuration	2022-01-24
EFO:0009782	progesterone-receptor positive breast cancer	skos:exactMatch	DOID:0060077	progesterone-receptor positive breast cancer	semapv:ManualMappingCuration	2023-12-04
EFO:0009783	carotid atherosclerosis	skos:exactMatch	DOID:9006778	Carotid Atherosclerosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009784	central serous retinopathy	skos:exactMatch	DOID:9003248	Central Serous Chorioretinopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009797	lung disease associated with cystic fibrosis	skos:exactMatch	DOID:1485	cystic fibrosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009833	kidney injury	skos:exactMatch	DOID:557	kidney disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009839	bradypnea	skos:exactMatch	DOID:9003280	bradypnea	semapv:ManualMappingCuration	2023-12-04
EFO:0009840	tachypnea	skos:exactMatch	DOID:9008811	Tachypnea	semapv:ManualMappingCuration	2023-12-04
EFO:0009842	respiratory depression	skos:exactMatch	DOID:11162	respiratory failure	semapv:ManualMappingCuration	2023-12-04
EFO:0009845	catalepsy	skos:exactMatch	DOID:9003805	Catalepsy	semapv:ManualMappingCuration	2023-12-04
EFO:0009846	muscle cramp	skos:exactMatch	DOID:9000373	Muscle Cramp	semapv:ManualMappingCuration	2023-12-04
EFO:0009847	dizziness	skos:exactMatch	DOID:9004211	Dizziness	semapv:ManualMappingCuration	2023-12-04
EFO:0009851	muscle atrophy	skos:exactMatch	DOID:767	muscular atrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0009854	treatment resistant depression	skos:exactMatch	DOID:1826	epilepsy	semapv:ManualMappingCuration	2023-12-04
EFO:0009854	treatment resistant depression	skos:exactMatch	DOID:9007883	Depressive Disorder, Treatment-Resistant	semapv:ManualMappingCuration	2023-12-04
EFO:0009855	frontal fibrosing alopecia	skos:exactMatch	DOID:9000209	frontal fibrosing alopecia	semapv:ManualMappingCuration	2023-12-04
EFO:0009856	lichen planopilaris	skos:exactMatch	DOID:9001311	Lichen Planus Follicularis	semapv:ManualMappingCuration	2023-12-04
EFO:0009867	dysphoria	skos:exactMatch	DOID:9005268	dysphoria	semapv:ManualMappingCuration	2023-12-04
EFO:0009869	xerostomia	skos:exactMatch	DOID:9006511	Xerostomia	semapv:ManualMappingCuration	2023-12-04
EFO:0009870	bone metastasis	skos:exactMatch	DOID:9007482	Bone Metastasis	semapv:ManualMappingCuration	2023-12-04
EFO:0009875	thymus atrophy	skos:exactMatch	DOID:7350	thymic dysplasia	semapv:ManualMappingCuration	2023-12-04
EFO:0009879	gastric hemorrhage	skos:exactMatch	DOID:9007598	gastric hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0009881	nonischemic cardiomyopathy	skos:exactMatch	DOID:9003717	nonischemic cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0009894	carbamazepine-induced hyponatremia	skos:exactMatch	DOID:9006635	Hyponatremia	semapv:ManualMappingCuration	2023-12-04
EFO:0009895	oxcarbazepine-induced hyponatremia	skos:exactMatch	DOID:9006635	Hyponatremia	semapv:ManualMappingCuration	2023-12-04
EFO:0009903	inflammatory disease	skos:exactMatch	DOID:9005372	Inflammation	semapv:ManualMappingCuration	2023-12-04
EFO:0009904	Lopes-Maciel-Rodan syndrome	skos:exactMatch	DOID:9000409	Lopes-Maciel-Rodan Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009907	Desmoid-type fibromatosis	skos:exactMatch	DOID:0080366	desmoid tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0009908	glabellar hemangioma	skos:exactMatch	DOID:255	hemangioma	semapv:ManualMappingCuration	2023-12-04
EFO:0009909	stage 5 chronic kidney disease	skos:exactMatch	DOID:783	end stage renal disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009910	chronic lung disease	skos:exactMatch	DOID:850	lung disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009911	hereditary nonpolyposis colorectal carcinoma	skos:exactMatch	DOID:3883	Lynch syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0009912	distal lower limb amyotrophy	skos:exactMatch	DOID:767	muscular atrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0009912	distal lower limb amyotrophy	skos:exactMatch	DOID:913	atrophic muscular disease	semapv:ManualMappingCuration	2023-12-04
EFO:0009948	chorioamnionitis	skos:exactMatch	DOID:0050697	chorioamnionitis	semapv:ManualMappingCuration	2022-01-24
EFO:0009953	post-operative myocardial infarction	skos:exactMatch	DOID:5844	myocardial infarction	semapv:ManualMappingCuration	2023-12-04
EFO:0009954	post-operative delirium	skos:exactMatch	DOID:9006358	Postoperative Cognitive Dysfunction	semapv:ManualMappingCuration	2023-12-04
EFO:0009955	post-operative acute kidney injury	skos:exactMatch	DOID:3021	acute kidney failure	semapv:ManualMappingCuration	2023-12-04
EFO:0009956	post-operative stroke	skos:exactMatch	DOID:9007096	Stroke	semapv:ManualMappingCuration	2023-12-04
EFO:0009959	diverticular disease	skos:exactMatch	DOID:9007768	Colonic Diverticulosis	semapv:ManualMappingCuration	2023-12-04
EFO:0009960	atypical femoral fracture	skos:exactMatch	DOID:9001166	atypical femoral fracture	semapv:ManualMappingCuration	2023-12-04
EFO:0009963	bipolar I disorder	skos:exactMatch	DOID:14042	bipolar I disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0009964	bipolar II disorder	skos:exactMatch	DOID:0060166	bipolar ll disorder	semapv:ManualMappingCuration	2022-01-24
EFO:0009965	Schizoaffective disorder-bipolar type	skos:exactMatch	DOID:9002705	schizoaffective disorder, bipolar type	semapv:ManualMappingCuration	2023-12-04
EFO:0010060	chronic human papillomavirus infection	skos:exactMatch	DOID:11166	papillomavirus infectious disease	semapv:ManualMappingCuration	2023-12-04
EFO:0010072	toothache	skos:exactMatch	DOID:9008251	Toothache	semapv:ManualMappingCuration	2023-12-04
EFO:0010098	stress-related disorder	skos:exactMatch	DOID:9001131	stress-related disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0010099	chronic widespread pain	skos:exactMatch	DOID:9008520	Chronic Pain	semapv:ManualMappingCuration	2023-12-04
EFO:0010100	multisite chronic pain	skos:exactMatch	DOID:9008520	Chronic Pain	semapv:ManualMappingCuration	2023-12-04
EFO:0010133	diabetic maculopathy	skos:exactMatch	DOID:9003638	diabetic maculopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0010143	chronic mountain sickness	skos:exactMatch	DOID:9005785	Altitude Sickness	semapv:ManualMappingCuration	2023-12-04
EFO:0010163	dilatation of the sinus of Valsalva	skos:exactMatch	DOID:14004	thoracic aortic aneurysm	semapv:ManualMappingCuration	2023-12-04
EFO:0010164	insulin-resistant diabetes mellitus	skos:exactMatch	DOID:9352	type 2 diabetes mellitus	semapv:ManualMappingCuration	2023-12-04
EFO:0010166	Warburg-Cinotti syndrome	skos:exactMatch	DOID:9000662	Warburg-Cinotti Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010167	squalene synthase deficiency	skos:exactMatch	DOID:9007732	Squalene Synthase Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0010168	spondyloepiphyseal dysplasia, Kondo-Fu type	skos:exactMatch	DOID:0112283	spondyloepiphyseal dysplasia Kondo-Fu type	semapv:ManualMappingCuration	2023-12-04
EFO:0010176	keratinocyte carcinoma	skos:exactMatch	DOID:3451	skin carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:0010177	lobar intracerebral hemorrhage	skos:exactMatch	DOID:9006918	lobar intracerebral hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0010178	non-lobar intracerebral hemorrhage	skos:exactMatch	DOID:9002676	Cerebral Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0010238	perinatal disease	skos:exactMatch	DOID:9003548	Infant, Newborn, Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0010248	spinocerebellar ataxia, autosomal recessive, 27	skos:exactMatch	DOID:0111616	autosomal recessive spinocerebellar ataxia 27	semapv:ManualMappingCuration	2023-12-04
EFO:0010249	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3	skos:exactMatch	DOID:0070465	spinocerebellar ataxia with axonal neuropathy type 3	semapv:ManualMappingCuration	2023-12-04
EFO:0010250	polydactyly, postaxial, A9	skos:exactMatch	DOID:9002200	Postaxial Polydactyly, Type A9	semapv:ManualMappingCuration	2023-12-04
EFO:0010251	spinocerebellar ataxia 48	skos:exactMatch	DOID:0111746	cerebellar ataxia type 48	semapv:ManualMappingCuration	2023-12-04
EFO:0010252	Menke-Hennekam syndrome 1	skos:exactMatch	DOID:9008974	Menke-Hennekam Syndrome 1	semapv:ManualMappingCuration	2023-12-04
EFO:0010253	Menke-Hennekam syndrome 2	skos:exactMatch	DOID:9000493	Menke-Hennekam Syndrome 2	semapv:ManualMappingCuration	2023-12-04
EFO:0010255	metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression	skos:exactMatch	DOID:9007390	Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression	semapv:ManualMappingCuration	2023-12-04
EFO:0010256	neurodegeneration, childhood-onset, with cerebellar atrophy	skos:exactMatch	DOID:9000084	Childhood-Onset Neurodegeneration with Cerebellar Atrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0010257	global developmental delay, progressive ataxia, and elevated glutamine	skos:exactMatch	DOID:9005979	Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine	semapv:ManualMappingCuration	2023-12-04
EFO:0010258	inflammatory bowel disease, immunodeficiency, and encephalopathy	skos:exactMatch	DOID:9009237	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY	semapv:ManualMappingCuration	2023-12-04
EFO:0010259	intellectual developmental disorder with macrocephaly, seizures, and speech delay	skos:exactMatch	DOID:9009239	Intellectual Developmental Disorder with Macrocephaly, Seizures, and Speech Delay	semapv:ManualMappingCuration	2023-12-04
EFO:0010260	global developmental delay with or without impaired intellectual development	skos:exactMatch	DOID:9008363	GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	semapv:ManualMappingCuration	2023-12-04
EFO:0010261	Paganini-Miozzo syndrome	skos:exactMatch	DOID:0111843	Paganini-Miozzo syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010262	leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate	skos:exactMatch	DOID:9000912	Acute Reversible Leukoencephalopathy with Increased Urinary Alpha-ketoglutarate	semapv:ManualMappingCuration	2023-12-04
EFO:0010263	gastrointestinal ulceration, recurrent, with dysfunctional platelets	skos:exactMatch	DOID:9000368	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	semapv:ManualMappingCuration	2023-12-04
EFO:0010264	spinal muscular atrophy, lower extremity-predominant, 2B, prenatal onset, autosomal dominant	skos:exactMatch	DOID:0070350	spinal muscular atrophy with lower extremity predominant 2B	semapv:ManualMappingCuration	2023-12-04
EFO:0010266	Charcot-Marie-Tooth disease type 1G	skos:exactMatch	DOID:0111560	Charcot-Marie-Tooth disease type 1G	semapv:ManualMappingCuration	2023-12-04
EFO:0010267	autosomal dominant intermediate Charcot-Marie-Tooth disease type G	skos:exactMatch	DOID:0080294	Charcot-Marie-Tooth disease dominant intermediate G	semapv:ManualMappingCuration	2023-12-04
EFO:0010268	brain abnormalities, neurodegeneration, and dysosteosclerosis	skos:exactMatch	DOID:9005822	BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS	semapv:ManualMappingCuration	2023-12-04
EFO:0010269	amenorrhea	skos:exactMatch	DOID:13938	amenorrhea	semapv:ManualMappingCuration	2023-12-04
EFO:0010274	thoracic aortic artery calcification	skos:exactMatch	DOID:9000815	Aortic Calcification	semapv:ManualMappingCuration	2023-12-04
EFO:0010276	neurodevelopmental disorder with seizures and non-epileptic hyperkinetic movements	skos:exactMatch	DOID:9001474	Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements	semapv:ManualMappingCuration	2023-12-04
EFO:0010277	O'Donnell-Luria-Rodan syndrome	skos:exactMatch	DOID:9001969	O'Donnell-Luria-Rodan Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010278	Shukla-Vernon syndrome	skos:exactMatch	DOID:0111841	Shukla-Vernon syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010279	GIST-plus syndrome	skos:exactMatch	DOID:9008257	Multiple Polyps and Recurrent Inflammatory Fibroid, Gastrointestinal	semapv:ManualMappingCuration	2023-12-04
EFO:0010280	intellectual developmental disorder, autosomal recessive 71	skos:exactMatch	DOID:0081232	autosomal recessive intellectual developmental disorder 71	semapv:ManualMappingCuration	2023-12-04
EFO:0010282	gastrointestinal disease	skos:exactMatch	DOID:77	gastrointestinal system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0010283	blood disease	skos:exactMatch	DOID:74	hematopoietic system disease	semapv:ManualMappingCuration	2023-12-04
EFO:0010284	hepatobiliary disease	skos:exactMatch	DOID:3118	hepatobiliary disease	semapv:ManualMappingCuration	2022-01-24
EFO:0010285	integumentary system disease	skos:exactMatch	DOID:16	integumentary system disease	semapv:ManualMappingCuration	2022-01-24
EFO:0010445	cocaine use disorder	skos:exactMatch	DOID:9005632	Cocaine-Related Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0010560	neurodevelopmental disorder with ataxia, hypotonia, and microcephaly	skos:exactMatch	DOID:9008370	NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY	semapv:ManualMappingCuration	2023-12-04
EFO:0010561	neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies	skos:exactMatch	DOID:0070346	neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies	semapv:ManualMappingCuration	2023-12-04
EFO:0010562	neurodevelopmental disorder with cerebellar hypoplasia and spasticity	skos:exactMatch	DOID:9009083	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY	semapv:ManualMappingCuration	2023-12-04
EFO:0010563	neurodevelopmental disorder with structural brain anomalies and dysmorphic facies	skos:exactMatch	DOID:9002267	Neurodevelopmental Disorder with Structural Brain Anomalies and Dysmorphic Facies	semapv:ManualMappingCuration	2023-12-04
EFO:0010564	glycosylphosphatidylinositol biosynthesis defect 21	skos:exactMatch	DOID:9007893	Glycosylphosphatidylinositol Biosynthesis Defect 21	semapv:ManualMappingCuration	2023-12-04
EFO:0010565	myopathy, congenital, progressive, with scoliosis	skos:exactMatch	DOID:0081351	congenital myopathy 19	semapv:ManualMappingCuration	2023-12-04
EFO:0010566	intellectual developmental disorder 60 with seizures	skos:exactMatch	DOID:9000911	Autosomal Dominant Intellectual Developmental Disorder 60	semapv:ManualMappingCuration	2023-12-04
EFO:0010567	spastic tetraplegia and axial hypotonia, progressive	skos:exactMatch	DOID:9000578	SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE	semapv:ManualMappingCuration	2023-12-04
EFO:0010568	neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities	skos:exactMatch	DOID:9000637	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES	semapv:ManualMappingCuration	2023-12-04
EFO:0010580	blastic plasmacytoid dendritic cell neoplasm	skos:exactMatch	DOID:0081076	blastic plasmacytoid dendritic cell neoplasm	semapv:ManualMappingCuration	2023-04-17
EFO:0010581	organophosphate poisoning	skos:exactMatch	DOID:9005292	Organophosphate Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:0010582	Morton Neuroma	skos:exactMatch	DOID:9004916	Morton Neuroma	semapv:ManualMappingCuration	2023-12-04
EFO:0010630	intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies	skos:exactMatch	DOID:9003704	Intellectual Developmental Disorder with Nasal Speech, Dysmorphic Facies, and Variable Skeletal Anomalies	semapv:ManualMappingCuration	2023-12-04
EFO:0010631	neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies	skos:exactMatch	DOID:9001150	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES	semapv:ManualMappingCuration	2023-12-04
EFO:0010632	Lessel-Kubisch syndrome	skos:exactMatch	DOID:9004277	Lessel-Kubisch Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010633	Siddiqi syndrome	skos:exactMatch	DOID:0081273	Siddiqi syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010634	Snijders Blok-Fisher syndrome	skos:exactMatch	DOID:9004310	Snijders Blok-Fisher Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010635	Weiss-Kruszka syndrome	skos:exactMatch	DOID:9005848	WEISS-KRUSZKA SYNDROME	semapv:ManualMappingCuration	2023-12-04
EFO:0010636	pontocerebellar hypoplasia type 13	skos:exactMatch	DOID:0112332	pontocerebellar hypoplasia type 13	semapv:ManualMappingCuration	2023-12-04
EFO:0010638	atopic asthma	skos:exactMatch	DOID:9415	allergic asthma	semapv:ManualMappingCuration	2023-12-04
EFO:0010642	Neurodevelopmental disorder	skos:exactMatch	DOID:9004429	Neurodevelopmental Disorders	semapv:ManualMappingCuration	2023-12-04
EFO:0010643	Snijders Blok-Campeau syndrome	skos:exactMatch	DOID:9001540	Snijders Blok-Campeau Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010644	Developmental delay with variable intellectual impairment and behavioural abnormalities	skos:exactMatch	DOID:9004868	Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities	semapv:ManualMappingCuration	2023-12-04
EFO:0010645	Cardiac-urogenital syndrome	skos:exactMatch	DOID:9007788	Cardiac-Urogenital Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010646	genetic non-acquired premature ovarian failure	skos:exactMatch	DOID:0080873	primary ovarian insufficiency 16	semapv:ManualMappingCuration	2023-12-04
EFO:0010651	intellectual developmental disorder with impaired language and dysmorphic facies	skos:exactMatch	DOID:9001091	INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES	semapv:ManualMappingCuration	2023-12-04
EFO:0010652	intellectual developmental disorder with short stature and behavioral abnormalities	skos:exactMatch	DOID:0111674	intellectual developmental disorder with short stature and behavioral abnormalities	semapv:ManualMappingCuration	2022-01-24
EFO:0010653	intellectual developmental disorder with speech delay, autism and dysmorphic facies	skos:exactMatch	DOID:9008787	Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Facies	semapv:ManualMappingCuration	2023-12-04
EFO:0010654	intellectual developmental disorder, autosomal recessive 72	skos:exactMatch	DOID:0080765	autosomal recessive intellectual developmental disorder 72	semapv:ManualMappingCuration	2023-12-04
EFO:0010655	megabladder, congenital	skos:exactMatch	DOID:0112014	congenital megabladder	semapv:ManualMappingCuration	2023-12-04
EFO:0010656	mitochondrial complex V deficiency, nuclear type 6	skos:exactMatch	DOID:0111749	mitochondrial complex V (ATP synthase) deficiency nuclear type 6	semapv:ManualMappingCuration	2023-12-04
EFO:0010657	neurodevelopmental disorder with absent language and variable seizures	skos:exactMatch	DOID:9001367	NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES	semapv:ManualMappingCuration	2023-12-04
EFO:0010658	neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia	skos:exactMatch	DOID:9006418	NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA	semapv:ManualMappingCuration	2023-12-04
EFO:0010659	neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies	skos:exactMatch	DOID:9001002	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES	semapv:ManualMappingCuration	2023-12-04
EFO:0010660	neurodevelopmental disorder with macrocephaly and with or without seizures	skos:exactMatch	DOID:9004521	Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures	semapv:ManualMappingCuration	2023-12-04
EFO:0010661	neurodevelopmental disorder with non-specific brain abnormalities and with or without seizures	skos:exactMatch	DOID:9001694	NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES	semapv:ManualMappingCuration	2023-12-04
EFO:0010662	neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies	skos:exactMatch	DOID:0070539	Halperin-Birk syndrome	semapv:ManualMappingCuration	2024-07-29
EFO:0010662	neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies	skos:exactMatch	DOID:9004325	Halperin-Birk Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010663	neurooculocardiogenitourinary syndrome	skos:exactMatch	DOID:0111675	neurooculocardiogenitourinary syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010664	pulmonary fibrosis, and/or bone marrow failure, telomere-related, 5	skos:exactMatch	DOID:9009112	Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome, Telomere-Related, 5	semapv:ManualMappingCuration	2023-12-04
EFO:0010665	short stature and microcephaly with genital anomalies	skos:exactMatch	DOID:9004567	Short Stature and Microcephaly with Genital Anomalies	semapv:ManualMappingCuration	2023-12-04
EFO:0010675	chronic venous hypertension	skos:exactMatch	DOID:9001465	chronic venous hypertension	semapv:ManualMappingCuration	2023-12-04
EFO:0010680	hematoma	skos:exactMatch	DOID:9006013	Hematoma	semapv:ManualMappingCuration	2023-12-04
EFO:0010684	malunion fracture	skos:exactMatch	DOID:9001758	Malunited Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:0010685	menopausal or post-menopausal disease	skos:exactMatch	DOID:229	female reproductive system disease	semapv:ManualMappingCuration	2023-12-04
EFO:0010687	neonatal erythema toxicum	skos:exactMatch	DOID:37	skin disease	semapv:ManualMappingCuration	2023-12-04
EFO:0010688	periapical tissue disease	skos:exactMatch	DOID:9002699	Periapical Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:0010689	perineum disease	skos:exactMatch	DOID:7	disease of anatomical entity	semapv:ManualMappingCuration	2023-12-04
EFO:0010693	tooth-supporting structures disease	skos:exactMatch	DOID:3388	periodontal disease	semapv:ManualMappingCuration	2023-12-04
EFO:0010698	retinal break	skos:exactMatch	DOID:12514	retinal perforation	semapv:ManualMappingCuration	2023-12-04
EFO:0010702	opioid use disorder	skos:exactMatch	DOID:11206	opioid abuse	semapv:ManualMappingCuration	2023-12-04
EFO:0010716	coinfection	skos:exactMatch	DOID:9000465	Coinfection	semapv:ManualMappingCuration	2023-12-04
EFO:0010723	ocular sarcoidosis	skos:exactMatch	DOID:9002459	ocular sarcoidosis	semapv:ManualMappingCuration	2023-12-04
EFO:0010737	autoinflammation with episodic fever and lymphadenopathy	skos:exactMatch	DOID:9004604	Autoinflammation with Episodic Fever and Lymphadenopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0010738	retinal dystrophy with leukodystrophy	skos:exactMatch	DOID:0080946	retinal dystrophy with leukodystrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0010739	epilepsy, early-onset, with or without developmental delay	skos:exactMatch	DOID:0070471	early-onset epilepsy 2	semapv:ManualMappingCuration	2023-12-04
EFO:0010740	Diets-Jongmans syndrome	skos:exactMatch	DOID:9005801	Diets-Jongmans Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0010820	spontaneous coronary artery dissection	skos:exactMatch	DOID:9005332	Spontaneous Coronary Artery Dissection	semapv:ManualMappingCuration	2023-12-04
EFO:0010822	stenosing tenosynovitis	skos:exactMatch	DOID:9004608	Tendon Entrapment	semapv:ManualMappingCuration	2023-12-04
EFO:0010826	cystine urolithiasis	skos:exactMatch	DOID:9266	cystinuria	semapv:ManualMappingCuration	2023-12-04
EFO:0010828	myofibrillar myopathy 9 with early respiratory failure	skos:exactMatch	DOID:0111188	myofibrillar myopathy 9	semapv:ManualMappingCuration	2023-12-04
EFO:0010830	lobular capilliary hemangioma	skos:exactMatch	DOID:9001866	Pyogenic Granuloma	semapv:ManualMappingCuration	2023-12-04
EFO:0010831	testicular mixed germ cell tumor	skos:exactMatch	DOID:4743	mixed testicular germ cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:0010832	primary central chondrosarcoma	skos:exactMatch	DOID:0050897	bone chondrosarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:0010833	uterine corpus undifferentiated sarcoma	skos:exactMatch	DOID:5165	uterine corpus sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:0010941	metastasis sample	skos:exactMatch	DOID:9000965	Neoplasm Metastasis	semapv:ManualMappingCuration	2023-12-04
EFO:0010953	autosomal recessive dilated cardiomyopathy	skos:exactMatch	DOID:12930	dilated cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0010954	cask-related x-linked intellectual disability	skos:exactMatch	DOID:0060807	syndromic X-linked intellectual disability Najm type	semapv:ManualMappingCuration	2023-12-04
EFO:0010954	cask-related x-linked intellectual disability	skos:exactMatch	DOID:9001153	FG Syndrome 4	semapv:ManualMappingCuration	2023-12-04
EFO:0010955	muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	skos:exactMatch	DOID:0112381	muscular dystrophy-dystroglycanopathy type C12	semapv:ManualMappingCuration	2023-12-04
EFO:0010956	peroxisome biogenesis disorder, complementation group 7	skos:exactMatch	DOID:906	peroxisomal disease	semapv:ManualMappingCuration	2023-12-04
EFO:0010977	macrovascular complications of diabetes	skos:exactMatch	DOID:11713	diabetic angiopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0011023	concussion	skos:exactMatch	DOID:9008967	Brain Concussion	semapv:ManualMappingCuration	2023-12-04
EFO:0011047	central nervous system toxicity	skos:exactMatch	DOID:9000948	central nervous system toxicity	semapv:ManualMappingCuration	2023-12-04
EFO:0011049	drug misuse	skos:exactMatch	DOID:302	substance abuse	semapv:ManualMappingCuration	2023-12-04
EFO:0011050	gastrointestinal toxicity	skos:exactMatch	DOID:9008632	gastrointestinal toxicity	semapv:ManualMappingCuration	2023-12-04
EFO:0011052	hepatotoxicity	skos:exactMatch	DOID:9007383	Chemical and Drug Induced Liver Injury	semapv:ManualMappingCuration	2023-12-04
EFO:0011054	metabolic toxicity	skos:exactMatch	DOID:0014667	disease of metabolism	semapv:ManualMappingCuration	2023-12-04
EFO:0011055	musculoskeletal toxicity	skos:exactMatch	DOID:9008906	Myotoxicity	semapv:ManualMappingCuration	2023-12-04
EFO:0011056	nephrotoxicity	skos:exactMatch	DOID:9006956	nephrotoxicity	semapv:ManualMappingCuration	2023-12-04
EFO:0011057	neurotoxicity	skos:exactMatch	DOID:9007553	neurotoxicity	semapv:ManualMappingCuration	2023-12-04
EFO:0011059	psychiatric toxicity	skos:exactMatch	DOID:303	substance-related disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0011060	respiratory toxicity	skos:exactMatch	DOID:9001219	respiratory toxicity	semapv:ManualMappingCuration	2023-12-04
EFO:0011062	vascular toxicity	skos:exactMatch	DOID:9007471	vascular toxicity	semapv:ManualMappingCuration	2023-12-04
EFO:0011063	recessive lissencephaly	skos:exactMatch	DOID:0050453	lissencephaly	semapv:ManualMappingCuration	2023-12-04
EFO:0011064	recessive spherocytosis	skos:exactMatch	DOID:12971	hereditary spherocytosis	semapv:ManualMappingCuration	2023-12-04
EFO:0020000	developmental and epileptic encephalopathy 94	skos:exactMatch	DOID:0081325	developmental and epileptic encephalopathy 94	semapv:ManualMappingCuration	2023-12-04
EFO:0020003	drug toxicity	skos:exactMatch	DOID:9006810	Drug-Related Side Effects and Adverse Reactions	semapv:ManualMappingCuration	2023-12-04
EFO:0020005	pheochromocytoma-paraganglioma	skos:exactMatch	DOID:0050773	paraganglioma	semapv:ManualMappingCuration	2023-12-04
EFO:0020006	enterocele	skos:exactMatch	DOID:1283	enterocele	semapv:ManualMappingCuration	2022-01-24
EFO:0020025	central hypoventilation syndrome, late-onset	skos:exactMatch	DOID:0060731	congenital central hypoventilation syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0020026	autosomal recessive retinitis pigmentosa	skos:exactMatch	DOID:10584	retinitis pigmentosa	semapv:ManualMappingCuration	2023-12-04
EFO:0020027	susceptibility to partial acquired lipodystrophy	skos:exactMatch	DOID:0080299	partial lipodystrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0020028	autosomal dominant retinitis pigmentosa	skos:exactMatch	DOID:10584	retinitis pigmentosa	semapv:ManualMappingCuration	2023-12-04
EFO:0020029	autosomal recessive cone rod dystrophy	skos:exactMatch	DOID:0050572	cone-rod dystrophy	semapv:ManualMappingCuration	2023-12-04
EFO:0020030	tubulinopathy	skos:exactMatch	DOID:0112227	tubulinopathy	semapv:ManualMappingCuration	2022-01-24
EFO:0020031	mononeuropathy of the median nerve	skos:exactMatch	DOID:571	median neuropathy	semapv:ManualMappingCuration	2023-12-04
EFO:0020032	autosomal recessive transient neonatal diabetes mellitus	skos:exactMatch	DOID:0060334	transient neonatal diabetes mellitus	semapv:ManualMappingCuration	2023-12-04
EFO:0020034	familial Behcet-like autoinflammatory syndrome	skos:exactMatch	DOID:0080944	familial Behcet-like autoinflammatory syndrome 1	semapv:ManualMappingCuration	2022-01-24
EFO:0020035	autosomal dominant common variable immunodeficiency	skos:exactMatch	DOID:12177	common variable immunodeficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0020036	autosomal recessive nemaline myopathy	skos:exactMatch	DOID:3191	nemaline myopathy	semapv:ManualMappingCuration	2023-12-04
EFO:0020037	autosominal recessive combined pituitary hormone deficiency	skos:exactMatch	DOID:9003666	Combined Pituitary Hormone Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:0020037	autosominal recessive combined pituitary hormone deficiency	skos:exactMatch	DOID:9410	panhypopituitarism	semapv:ManualMappingCuration	2024-07-29
EFO:0020038	megacystis-microcolon-intestinal hypoperistalsis syndrome 5	skos:exactMatch	DOID:9000803	Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 5	semapv:ManualMappingCuration	2023-12-04
EFO:0020039	neuronal ceroid-lipofuscinosis, dominant/recessive	skos:exactMatch	DOID:891	progressive myoclonus epilepsy	semapv:ManualMappingCuration	2023-12-04
EFO:0020040	transient neonatal diabetes, dominant/recessive	skos:exactMatch	DOID:0060334	transient neonatal diabetes mellitus	semapv:ManualMappingCuration	2023-12-04
EFO:0020041	congenital myasthenic syndrome, dominant/recessive	skos:exactMatch	DOID:3635	congenital myasthenic syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0020092	neuroinflammatory disorder	skos:exactMatch	DOID:0060004	autoimmune disease of central nervous system	semapv:ManualMappingCuration	2023-04-17
EFO:0020101	parenchymal hematoma	skos:exactMatch	DOID:9002676	Cerebral Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:0020858	spastic paraplegia 84, autosomal recessive	skos:exactMatch	DOID:0112347	hereditary spastic paraplegia 84	semapv:ManualMappingCuration	2023-12-04
EFO:0020910	thermal burn	skos:exactMatch	DOID:9007730	Burns	semapv:ManualMappingCuration	2023-12-04
EFO:0020911	overdose	skos:exactMatch	DOID:9001189	Drug Overdose	semapv:ManualMappingCuration	2023-12-04
EFO:0020914	disorientation	skos:exactMatch	DOID:9000348	Confusion	semapv:ManualMappingCuration	2023-12-04
EFO:0020915	uterine hyperstimulation	skos:exactMatch	DOID:9004403	uterine hyperstimulation	semapv:ManualMappingCuration	2023-12-04
EFO:0020918	non-allergic anaphylaxis	skos:exactMatch	DOID:9007278	Anaphylaxis	semapv:ManualMappingCuration	2023-12-04
EFO:0020919	subacute myelo-opticoneuropathy	skos:exactMatch	DOID:1289	neurodegenerative disease	semapv:ManualMappingCuration	2023-12-04
EFO:0020921	hemorrhagic stroke	skos:exactMatch	DOID:9000627	hemorrhagic stroke	semapv:ManualMappingCuration	2023-12-04
EFO:0020924	intentional overdose	skos:exactMatch	DOID:9001189	Drug Overdose	semapv:ManualMappingCuration	2023-12-04
EFO:0020925	angina unstable	skos:exactMatch	DOID:8805	intermediate coronary syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:0020926	noninfective encephalitis	skos:exactMatch	DOID:9588	encephalitis	semapv:ManualMappingCuration	2023-12-04
EFO:0020927	skin reaction	skos:exactMatch	DOID:2773	contact dermatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0020937	inherited macular dystrophy	skos:exactMatch	DOID:4448	macular degeneration	semapv:ManualMappingCuration	2023-12-04
EFO:0020971	internalizing disorder	skos:exactMatch	DOID:9001431	internalizing disorder	semapv:ManualMappingCuration	2023-12-04
EFO:0021425	pigmentary glaucoma	skos:exactMatch	DOID:1067	open-angle glaucoma	semapv:ManualMappingCuration	2023-12-04
EFO:0021431	adult hypophosphatasia	skos:exactMatch	DOID:0110913	adult hypophosphatasia	semapv:ManualMappingCuration	2022-07-21
EFO:0021432	childhood-onset hypophosphatasia	skos:exactMatch	DOID:0110915	childhood hypophosphatasia	semapv:ManualMappingCuration	2023-12-04
EFO:0021433	congenital chronic kidney disease	skos:exactMatch	DOID:784	chronic kidney disease	semapv:ManualMappingCuration	2023-12-04
EFO:0021524	non-alcoholic pancreatitis	skos:exactMatch	DOID:4989	pancreatitis	semapv:ManualMappingCuration	2023-12-04
EFO:0021525	renal overload-type gout	skos:exactMatch	DOID:13189	gout	semapv:ManualMappingCuration	2023-12-04
EFO:0021797	infantile hypophosphatasia	skos:exactMatch	DOID:0110914	infantile hypophosphatasia	semapv:ManualMappingCuration	2023-03-06
EFO:0021801	x-linked warfarin sensitivity	skos:exactMatch	DOID:0080839	X-linked warfarin sensitivity	semapv:ManualMappingCuration	2023-03-06
EFO:0030050	death from disease	skos:exactMatch	DOID:9000543	Death	semapv:ManualMappingCuration	2023-12-04
EFO:0030051	death from other causes	skos:exactMatch	DOID:9000543	Death	semapv:ManualMappingCuration	2023-12-04
EFO:0600032	congenital right-sided heart lesions	skos:exactMatch	DOID:9008565	Congenital Heart Defects, Multiple Types	semapv:ManualMappingCuration	2023-12-04
EFO:0600078	Achilles tendon injury	skos:exactMatch	DOID:9008331	Tendon Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:0600095	primary dental caries	skos:exactMatch	DOID:217	enamel caries	semapv:ManualMappingCuration	2023-12-04
EFO:0600096	permanent dental caries	skos:exactMatch	DOID:216	dental caries	semapv:ManualMappingCuration	2023-12-04
EFO:0700020	Birt-Hogg-Dube syndrome	skos:exactMatch	DOID:0050676	Birt-Hogg-Dube syndrome	semapv:ManualMappingCuration	2023-12-24
EFO:0700022	lysosomal acid lipase deficiency	skos:exactMatch	DOID:0080217	lysosomal acid lipase deficiency	semapv:ManualMappingCuration	2023-12-24
EFO:1000003	Zinc deficiency	skos:exactMatch	DOID:9003921	Zinc Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1000012	Rienhoff syndrome	skos:exactMatch	DOID:0070236	Loeys-Dietz syndrome 5	semapv:ManualMappingCuration	2022-01-24
EFO:1000013	Prinzmetal's angina	skos:exactMatch	DOID:0111151	Prinzmetal angina	semapv:ManualMappingCuration	2022-01-24
EFO:1000014	acidosis	skos:exactMatch	DOID:9002802	Acidoses	semapv:ManualMappingCuration	2023-12-04
EFO:1000016	anaplastic lung carcinoma	skos:exactMatch	DOID:4556	lung large cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000017	autosomal recessive disease	skos:exactMatch	DOID:0050737	autosomal recessive disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000018	bladder disease	skos:exactMatch	DOID:365	bladder disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000019	breast synovial sarcoma	skos:exactMatch	DOID:5485	synovial sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000020	cecum adenocarcinoma	skos:exactMatch	DOID:3039	cecum adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000021	cecum carcinoma	skos:exactMatch	DOID:1519	cecum carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000023	chronic cystitis	skos:exactMatch	DOID:1680	chronic cystitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000024	chronic rhinosinusitis	skos:exactMatch	DOID:9006771	Chronic Rhinosinusitis	semapv:ManualMappingCuration	2023-12-04
EFO:1000025	cystitis	skos:exactMatch	DOID:1679	cystitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000026	diffuse intrinsic pontine glioma	skos:exactMatch	DOID:0080684	diffuse midline glioma, H3 K27M-mutant	semapv:ManualMappingCuration	2023-12-04
EFO:1000026	diffuse intrinsic pontine glioma	skos:exactMatch	DOID:9004158	diffuse intrinsic pontine glioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000027	ependymal neoplasm	skos:exactMatch	DOID:9005834	Ependymomas	semapv:ManualMappingCuration	2023-12-04
EFO:1000028	ependymoma	skos:exactMatch	DOID:4844	benign ependymoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000028	ependymoma	skos:exactMatch	DOID:9005834	Ependymomas	semapv:ManualMappingCuration	2023-12-04
EFO:1000029	gastric adenosquamous carcinoma	skos:exactMatch	DOID:5635	gastric adenosquamous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000030	gastric tubular adenocarcinoma	skos:exactMatch	DOID:6595	gastric tubular adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000032	granulosa cell tumor	skos:exactMatch	DOID:2999	granulosa cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000034	indeterminate colitis	skos:exactMatch	DOID:9003001	indeterminate colitis	semapv:ManualMappingCuration	2023-12-04
EFO:1000035	infectious colitis	skos:exactMatch	DOID:9000192	infectious colitis	semapv:ManualMappingCuration	2023-12-04
EFO:1000036	lactic acidosis	skos:exactMatch	DOID:3650	lactic acidosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000037	lung carcinoid tumor	skos:exactMatch	DOID:9006608	Lung Carcinoid Tumors	semapv:ManualMappingCuration	2023-12-04
EFO:1000039	meningeal tuberculosis	skos:exactMatch	DOID:9004501	Meningeal Tuberculosis	semapv:ManualMappingCuration	2023-12-04
EFO:1000040	metaplastic breast carcinoma	skos:exactMatch	DOID:4680	breast metaplastic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000041	nephrosclerosis	skos:exactMatch	DOID:11664	nephrosclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000042	ovarian clear cell adenocarcinoma	skos:exactMatch	DOID:5304	ovarian clear cell adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000043	ovarian serous cystadenocarcinoma	skos:exactMatch	DOID:5746	ovarian serous cystadenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000044	pancreatic adenocarcinoma	skos:exactMatch	DOID:4074	pancreatic adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000045	pancreatic neuroendocrine tumor	skos:exactMatch	DOID:1799	islet cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000046	papillary lung adenocarcinoma	skos:exactMatch	DOID:5588	lung papillary adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000047	pleomorphic breast carcinoma	skos:exactMatch	DOID:9004951	breast pleomorphic carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000048	postweaning multisystemic wasting syndrome	skos:exactMatch	DOID:9002827	Porcine Postweaning Multisystemic Wasting Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1000049	pulmonary tuberculosis	skos:exactMatch	DOID:2957	pulmonary tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000050	renal leiomyoma	skos:exactMatch	DOID:127	leiomyoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000051	reproductive system neoplasm	skos:exactMatch	DOID:9008651	reproductive system neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000052	sex cord-stromal tumor	skos:exactMatch	DOID:192	sex cord-gonadal stromal tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000053	squamous cell breast carcinoma	skos:exactMatch	DOID:5514	breast squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000054	thymic lymphoma	skos:exactMatch	DOID:10146	thymus lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000055	tongue squamous cell carcinoma	skos:exactMatch	DOID:0050865	tongue squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000057	nasal cavity squamous cell carcinoma	skos:exactMatch	DOID:5515	nasal cavity squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000058	nasopharyngeal squamous cell carcinoma	skos:exactMatch	DOID:9009187	Aerodigestive Tract Squamous Cell Carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000059	cervical artery dissection	skos:exactMatch	DOID:9001528	ARTERIAL DISSECTION	semapv:ManualMappingCuration	2023-12-04
EFO:1000060	intestinal disaccharide deficiency and disaccharide malabsorption	skos:exactMatch	DOID:9868	intestinal disaccharidase deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:1000062	lactose intolerance	skos:exactMatch	DOID:10604	lactose intolerance	semapv:ManualMappingCuration	2022-01-24
EFO:1000063	lactose intolerance adult type	skos:exactMatch	DOID:9006147	Lactose Intolerance, Adult Type	semapv:ManualMappingCuration	2023-12-04
EFO:1000064	Acinar Prostate Adenocarcinoma, Foamy Gland Variant	skos:exactMatch	DOID:3024	prostatic acinar adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000065	Acinar Prostate Mucinous Adenocarcinoma	skos:exactMatch	DOID:3703	prostate colloid adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000066	ACTH-Producing Pituitary Gland Adenoma	skos:exactMatch	DOID:7004	ACTH-secreting pituitary adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000067	ACTH-Producing Pituitary Gland Carcinoma	skos:exactMatch	DOID:6276	malignant ACTH producing neoplasm of pituitary gland	semapv:ManualMappingCuration	2022-01-24
EFO:1000068	Acute Leukemia	skos:exactMatch	DOID:12603	acute leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1000069	Adamantinomatous Craniopharyngioma	skos:exactMatch	DOID:3846	adamantinous craniopharyngioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000070	Adenofibroma	skos:exactMatch	DOID:2683	adenofibroma	semapv:ManualMappingCuration	2022-01-24
EFO:1000071	Adenoid Cystic Breast Carcinoma	skos:exactMatch	DOID:4877	breast adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000072	Adenomatoid Odontogenic Tumor	skos:exactMatch	DOID:9008065	Adenoameloblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000073	Adenosquamous Carcinoma	skos:exactMatch	DOID:4830	adenosquamous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000074	Adrenal Gland Myelolipoma	skos:exactMatch	DOID:9000055	Myelolipoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000075	Adrenal Gland Neuroblastoma	skos:exactMatch	DOID:5718	adrenal neuroblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000076	Adrenal Medullary Hyperplasia	skos:exactMatch	DOID:9004344	Adrenal Medullary Hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000077	AIDS-Related Primary Central Nervous System Lymphoma	skos:exactMatch	DOID:9000242	Lymphoma, AIDS-Related	semapv:ManualMappingCuration	2023-12-04
EFO:1000078	Ameloblastic Carcinoma	skos:exactMatch	DOID:9005407	Ameloblastic Carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000079	Ampulla of Vater Carcinoma	skos:exactMatch	DOID:4932	ampulla of Vater carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000080	Anal Melanoma	skos:exactMatch	DOID:14145	malignant anus melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000081	Anal Squamous Cell Carcinoma	skos:exactMatch	DOID:5525	anal squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000082	Anaplastic (Malignant) Meningioma	skos:exactMatch	DOID:9005493	Anaplastic Meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000084	Angioleiomyoma	skos:exactMatch	DOID:4265	angiomyoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000085	Angiolipoma	skos:exactMatch	DOID:3616	angiolipoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000086	Angiomatous Meningioma	skos:exactMatch	DOID:6548	angiomatous meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000087	Angiomyxoma	skos:exactMatch	DOID:9003253	Myxoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000088	Appendix Adenocarcinoma	skos:exactMatch	DOID:3608	appendix adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000089	Appendix Adenoma	skos:exactMatch	DOID:11240	appendiceal neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000090	Appendix Goblet Cell Carcinoid	skos:exactMatch	DOID:0050911	appendix carcinoid tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000091	Appendix Hyperplastic Polyp	skos:exactMatch	DOID:9001642	Intestinal Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1000092	Appendix Neuroendocrine Tumor G1	skos:exactMatch	DOID:0050911	appendix carcinoid tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000093	Appendix Villous Adenoma	skos:exactMatch	DOID:11240	appendiceal neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000094	Ascending Colon Neuroendocrine Tumor G1	skos:exactMatch	DOID:9004109	Intestinal Carcinoid Tumors	semapv:ManualMappingCuration	2023-12-04
EFO:1000095	Askin Tumor	skos:exactMatch	DOID:0050608	Askin's tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000096	Atrophy	skos:exactMatch	DOID:9004462	Atrophy	semapv:ManualMappingCuration	2023-12-04
EFO:1000097	Atypical Carcinoid Tumor	skos:exactMatch	DOID:9007787	Carcinoid Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000098	Atypical Endometrial Hyperplasia	skos:exactMatch	DOID:0080365	endometrial hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000099	Atypical Lipomatous Tumor	skos:exactMatch	DOID:5690	well-differentiated liposarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000100	Atypical Lobular Breast Hyperplasia	skos:exactMatch	DOID:3010	lobular neoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000101	Atypical Meningioma	skos:exactMatch	DOID:9005143	Atypical Meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000102	B-Cell Prolymphocytic Leukemia	skos:exactMatch	DOID:0081041	B-cell prolymphocytic leukemia	semapv:ManualMappingCuration	2023-03-17
EFO:1000103	Bartholin Gland Carcinoma	skos:exactMatch	DOID:3999	Bartholin's gland carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000103	Bartholin Gland Carcinoma	skos:exactMatch	DOID:60003	Bartholin's gland cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000104	Bartholin Gland Squamous Cell Carcinoma	skos:exactMatch	DOID:6961	Bartholin's gland squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000106	Benign Adrenal Gland Pheochromocytoma	skos:exactMatch	DOID:0050771	pheochromocytoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000107	Benign Brain Neoplasm	skos:exactMatch	DOID:9007502	Brain Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000108	Benign Carotid Body Paraganglioma	skos:exactMatch	DOID:9002162	Carotid Body Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000110	Benign Conjunctival Neoplasm	skos:exactMatch	DOID:9007374	Benign Conjunctival Neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000111	Benign Kidney Neoplasm	skos:exactMatch	DOID:3116	kidney benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000112	Benign Ovarian Brenner Tumor	skos:exactMatch	DOID:2636	ovarian Brenner tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000113	Benign Ovarian Endometrioid Tumor	skos:exactMatch	DOID:0060112	ovarian benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000114	Benign Ovarian Mixed Epithelial Tumor	skos:exactMatch	DOID:6211	mixed epithelial tumor of ovary	semapv:ManualMappingCuration	2023-12-04
EFO:1000115	Benign Ovarian Mucinous Tumor	skos:exactMatch	DOID:9002755	Benign Ovarian Mucinous Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000116	Benign Ovarian Neoplasm	skos:exactMatch	DOID:0060112	ovarian benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000117	Benign Ovarian Surface Epithelial-Stromal Tumor	skos:exactMatch	DOID:0060112	ovarian benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000118	Benign Renal Pelvis Neoplasm	skos:exactMatch	DOID:5977	renal pelvis benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000119	Benign Salivary Gland Myoepithelioma	skos:exactMatch	DOID:9003216	Salivary Gland Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000121	Benign Smooth Muscle Neoplasm	skos:exactMatch	DOID:9002022	Benign Smooth Muscle Neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000122	Benign Thyroid Gland Neoplasm	skos:exactMatch	DOID:9007496	Thyroid Benign Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000123	Bile Duct Adenoma	skos:exactMatch	DOID:5381	bile duct adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000124	Biphasic Mesothelioma	skos:exactMatch	DOID:4486	malignant biphasic mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000125	Bladder Adenocarcinoma	skos:exactMatch	DOID:3711	bladder adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000126	Bladder Flat Intraepithelial Lesion	skos:exactMatch	DOID:5429	bladder flat intraepithelial lesion	semapv:ManualMappingCuration	2022-01-24
EFO:1000127	Bladder Inflammatory Myofibroblastic Tumor	skos:exactMatch	DOID:0050905	inflammatory myofibroblastic tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000128	Bladder Paraganglioma	skos:exactMatch	DOID:0050773	paraganglioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000129	Bladder Small Cell Neuroendocrine Carcinoma	skos:exactMatch	DOID:7132	urinary bladder small cell neuroendocrine carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000130	Bladder Squamous Cell Carcinoma	skos:exactMatch	DOID:3742	bladder squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000131	Blast Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive	skos:exactMatch	DOID:9002473	Blast Crisis	semapv:ManualMappingCuration	2023-12-04
EFO:1000132	Bone Epithelioid Hemangioma	skos:exactMatch	DOID:6610	bone epithelioid hemangioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000133	Borderline Exocrine Pancreatic Neoplasm	skos:exactMatch	DOID:9003100	Pancreatic Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000134	Borderline Fallopian Tube Serous Neoplasm	skos:exactMatch	DOID:0060111	fallopian tube benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000135	Borderline Ovarian Brenner Tumor	skos:exactMatch	DOID:2636	ovarian Brenner tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000136	Borderline Ovarian Clear Cell Tumor	skos:exactMatch	DOID:5390	clear cell adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000137	Borderline Ovarian Endometrioid Tumor	skos:exactMatch	DOID:9002762	Ovarian Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000138	Borderline Ovarian Mucinous Tumor	skos:exactMatch	DOID:6067	ovarian mucinous neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000139	Borderline Ovarian Serous Tumor	skos:exactMatch	DOID:9002762	Ovarian Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000140	Borderline Ovarian Surface Epithelial-Stromal Tumor	skos:exactMatch	DOID:9002762	Ovarian Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000141	Brain Stem Glioblastoma	skos:exactMatch	DOID:4202	brain stem glioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000142	Brain Stem Glioma	skos:exactMatch	DOID:4202	brain stem glioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000144	Breast Diffuse Large B-Cell Lymphoma	skos:exactMatch	DOID:0050745	diffuse large B-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000145	breast fibrosis	skos:exactMatch	DOID:10353	fibrosclerosis of breast	semapv:ManualMappingCuration	2022-01-24
EFO:1000146	Breast Mucosa-Associated Lymphoid Tissue Lymphoma	skos:exactMatch	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue	semapv:ManualMappingCuration	2023-12-04
EFO:1000148	Calcifying Fibrous Tumor	skos:exactMatch	DOID:0050871	fibroma	semapv:ManualMappingCuration	2023-12-04
EFO:1000149	Calcifying Nested Epithelial Stromal Tumor of the Liver	skos:exactMatch	DOID:686	liver carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000150	Cardiac Rhabdomyoma	skos:exactMatch	DOID:9006426	Cardiac Rhabdomyoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000151	Cavernous Hemangioma	skos:exactMatch	DOID:483	cavernous hemangioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000152	Cavernous Hemangioma of the Face	skos:exactMatch	DOID:5776	cavernous hemangioma of face	semapv:ManualMappingCuration	2022-01-24
EFO:1000154	Cecum Neuroendocrine Tumor G1	skos:exactMatch	DOID:4119	intestinal neuroendocrine benign tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000155	Cecum Villous Adenoma	skos:exactMatch	DOID:0050910	cecum adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000156	Central Nervous System Anaplastic Large Cell Lymphoma	skos:exactMatch	DOID:0050744	anaplastic large cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000157	Central Nervous System Lymphoma	skos:exactMatch	DOID:3234	central nervous system lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000158	Central Nervous System Neoplasm	skos:exactMatch	DOID:9007701	Central Nervous System Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000159	Cerebellar Liponeurocytoma	skos:exactMatch	DOID:6458	cerebellar liponeurocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000160	Cervical Adenoid Basal Carcinoma	skos:exactMatch	DOID:6428	cervical adenoid basal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000161	Cervical Adenoid Cystic Carcinoma	skos:exactMatch	DOID:4867	cervical adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000162	Cervical Adenosquamous Carcinoma	skos:exactMatch	DOID:5636	cervical adenosquamous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000163	Cervical Clear Cell Adenocarcinoma	skos:exactMatch	DOID:5303	cervical clear cell adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000164	Cervical Endometrioid Adenocarcinoma	skos:exactMatch	DOID:5830	cervical endometrioid adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000165	Cervical Glandular Intraepithelial Neoplasia	skos:exactMatch	DOID:9005612	Endometrial Intraepithelial Neoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000167	Cervical Large Cell Neuroendocrine Carcinoma	skos:exactMatch	DOID:6659	cervical large cell neuroendocrine carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000168	Cervical Metaplasia	skos:exactMatch	DOID:9000156	Metaplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000169	Cervical Mucinous Adenocarcinoma, Minimal Deviation Variant	skos:exactMatch	DOID:6627	cervical adenoma malignum	semapv:ManualMappingCuration	2022-01-24
EFO:1000170	Cervical Mucinous Adenocarcinoma, Villoglandular Variant	skos:exactMatch	DOID:8338	villoglandular variant cervical mucinous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000171	Cervical Small Cell Carcinoma	skos:exactMatch	DOID:6740	cervix small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000172	cervical squamous cell carcinoma	skos:exactMatch	DOID:3744	cervical squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000173	Cervical Wilms Tumor	skos:exactMatch	DOID:5190	cervical Wilms' tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000174	Chondroid Chordoma	skos:exactMatch	DOID:4152	chondroid chordoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000175	Chondroid Hamartoma	skos:exactMatch	DOID:9007253	Hamartoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000176	Chordoid Meningioma	skos:exactMatch	DOID:8368	chordoid meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000177	Choroid Plexus Papilloma	skos:exactMatch	DOID:2626	choroid plexus papilloma	semapv:ManualMappingCuration	2023-12-04
EFO:1000178	Chronic Eosinophilic Leukemia, Not Otherwise Specified	skos:exactMatch	DOID:0080367	chronic eosinophilic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1000179	Chronic Neutrophilic Leukemia	skos:exactMatch	DOID:0080187	chronic neutrophilic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1000180	Clear Cell Meningioma	skos:exactMatch	DOID:4210	clear cell meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000182	Colon Burkitt Lymphoma	skos:exactMatch	DOID:8584	Burkitt lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000183	Colon Dysplasia	skos:exactMatch	DOID:5353	colonic disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000184	Colon Inflammatory Polyp	skos:exactMatch	DOID:9006354	Colon Inflammatory Polyp	semapv:ManualMappingCuration	2023-12-04
EFO:1000185	Colon Juvenile Polyp	skos:exactMatch	DOID:9004271	Colonic Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1000188	Colon Neuroendocrine Tumor G1	skos:exactMatch	DOID:4118	colon neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000189	Colon Sessile Serrated Adenoma/Polyp	skos:exactMatch	DOID:9004271	Colonic Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1000190	Colorectal Adenosquamous Carcinoma	skos:exactMatch	DOID:5629	adenosquamous colon carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000191	Colorectal Diffuse Large B-Cell Lymphoma	skos:exactMatch	DOID:0050745	diffuse large B-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000192	Colorectal Gastrointestinal Stromal Tumor	skos:exactMatch	DOID:9253	gastrointestinal stromal tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000193	Colorectal Hamartoma	skos:exactMatch	DOID:9007253	Hamartoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000194	Colorectal Juvenile Polyp	skos:exactMatch	DOID:9001642	Intestinal Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1000195	Colorectal Neuroendocrine Tumor G1	skos:exactMatch	DOID:4118	colon neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000196	Colorectal Serrated Adenocarcinoma	skos:exactMatch	DOID:0050861	colorectal adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000197	Colorectal Sessile Serrated Adenoma/Polyp	skos:exactMatch	DOID:0050860	colorectal adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000198	Colorectal Squamous Cell Carcinoma	skos:exactMatch	DOID:5519	colon squamous cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000199	Columnar Cell Hyperplasia of the Breast	skos:exactMatch	DOID:9002221	Hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000200	Combined Lung Carcinoma	skos:exactMatch	DOID:1800	neuroendocrine carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000201	Common Hematopoietic Neoplasm	skos:exactMatch	DOID:9006532	Hematologic Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000202	Complex Endometrial Hyperplasia	skos:exactMatch	DOID:0080365	endometrial hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000203	Conjunctival Disorder	skos:exactMatch	DOID:4251	conjunctival disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000204	Conjunctival Melanoma	skos:exactMatch	DOID:1751	malignant conjunctival melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000205	Conjunctival Nevus	skos:exactMatch	DOID:0050906	conjunctival nevus	semapv:ManualMappingCuration	2022-01-24
EFO:1000206	Conjunctival Squamous Cell Carcinoma	skos:exactMatch	DOID:1748	conjunctival squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000208	Cortisol-Producing Adrenal Cortex Adenoma	skos:exactMatch	DOID:0050891	adrenal cortical adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000209	Craniopharyngioma	skos:exactMatch	DOID:3840	craniopharyngioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000210	Cribriform Carcinoma	skos:exactMatch	DOID:5675	cribriform carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000211	Cutaneous Follicular Lymphoma	skos:exactMatch	DOID:0050873	follicular lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000212	Cutaneous Undifferentiated Pleomorphic Sarcoma	skos:exactMatch	DOID:1906	malignant skin fibrous histiocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000213	Cystic Nephroma	skos:exactMatch	DOID:2673	adult cystic nephroma	semapv:ManualMappingCuration	2023-12-04
EFO:1000214	Dedifferentiated Solitary Fibrous Tumor	skos:exactMatch	DOID:9002958	Solitary Fibrous Tumors	semapv:ManualMappingCuration	2023-12-04
EFO:1000215	Desmoplastic Ameloblastoma	skos:exactMatch	DOID:9007904	Desmoplastic Ameloblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000216	Diffuse Melanocytosis	skos:exactMatch	DOID:6379	diffuse meningeal melanocytosis	semapv:ManualMappingCuration	2023-12-04
EFO:1000217	Digestive System Adenoma	skos:exactMatch	DOID:4147	gastrointestinal adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000218	Digestive System Carcinoma	skos:exactMatch	DOID:0050922	gastrointestinal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000219	Digestive System Mixed Adenoneuroendocrine Carcinoma	skos:exactMatch	DOID:9004351	Digestive System Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000220	Disseminated Peritoneal Leiomyomatosis	skos:exactMatch	DOID:5728	diffuse peritoneal leiomyomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000221	Ductal Breast Carcinoma In Situ and Lobular Carcinoma In Situ	skos:exactMatch	DOID:8791	breast carcinoma in situ	semapv:ManualMappingCuration	2023-12-04
EFO:1000223	Duodenal Adenocarcinoma	skos:exactMatch	DOID:10816	duodenum adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000224	Duodenal Gastrin-Producing Neuroendocrine Tumor	skos:exactMatch	DOID:7959	duodenal gastrinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000225	Duodenal Villous Adenoma	skos:exactMatch	DOID:0050927	duodenum adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000226	Dysplasia in Ulcerative Colitis	skos:exactMatch	DOID:9004831	Colitis-Associated Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000227	Dysplasia of Larynx	skos:exactMatch	DOID:786	laryngeal disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000228	EBV-Positive T-Cell Lymphoproliferative Disorder of Childhood	skos:exactMatch	DOID:0070324	systemic Epstein-Barr virus positive T-cell lymphoma of childhood	semapv:ManualMappingCuration	2023-12-04
EFO:1000229	Eccrine Porocarcinoma	skos:exactMatch	DOID:7566	eccrine porocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000230	Endolymphatic Sac Tumor	skos:exactMatch	DOID:4892	middle ear adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000231	Endometrial Clear Cell Adenocarcinoma	skos:exactMatch	DOID:5299	endometrial clear cell adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000232	Endometrial Cyst	skos:exactMatch	DOID:9007583	Cysts	semapv:ManualMappingCuration	2023-12-04
EFO:1000233	Endometrial Endometrioid Adenocarcinoma	skos:exactMatch	DOID:2870	endometrial adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000234	Endometrial Hyperplasia without Atypia	skos:exactMatch	DOID:9002840	Endometrial Hyperplasia without Atypia	semapv:ManualMappingCuration	2023-12-04
EFO:1000235	Endometrial Intraepithelial Neoplasia	skos:exactMatch	DOID:9005612	Endometrial Intraepithelial Neoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000236	Endometrial Mucinous Adenocarcinoma	skos:exactMatch	DOID:3707	endometrial mucinous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000237	Endometrial Polyp	skos:exactMatch	DOID:9042	polyp of corpus uteri	semapv:ManualMappingCuration	2023-12-04
EFO:1000238	Endometrial Serous Adenocarcinoma	skos:exactMatch	DOID:5750	endometrial serous adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000239	Endometrial Small Cell Carcinoma	skos:exactMatch	DOID:7139	endometrial small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000240	Endometrial Squamous Cell Carcinoma	skos:exactMatch	DOID:5533	endometrial squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000241	Endometrial Stromal Nodule	skos:exactMatch	DOID:1373	endometrial stromal nodule	semapv:ManualMappingCuration	2023-12-04
EFO:1000242	Endometrial Undifferentiated Carcinoma	skos:exactMatch	DOID:2871	endometrial carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000243	Epidermal Inclusion Cyst	skos:exactMatch	DOID:9005841	Epidermal Cyst	semapv:ManualMappingCuration	2023-12-04
EFO:1000244	Epithelioid Cell Uveal Melanoma	skos:exactMatch	DOID:7040	uveal epithelioid cell melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000245	Epithelioid Malignant Peripheral Nerve Sheath Tumor	skos:exactMatch	DOID:8353	epithelioid malignant peripheral nerve sheath tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000246	Ethmoid Sinus Adenoid Cystic Carcinoma	skos:exactMatch	DOID:2764	ethmoid sinus adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000247	Extrahepatic Bile Duct Adenosquamous Carcinoma	skos:exactMatch	DOID:5624	adenosquamous bile duct carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000248	Extrahepatic Bile Duct Squamous Cell Carcinoma	skos:exactMatch	DOID:5537	squamous cell bile duct carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000249	Extramammary Paget Disease	skos:exactMatch	DOID:3450	cutaneous Paget's disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000250	Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor	skos:exactMatch	DOID:4985	extraosseous Ewings sarcoma-primitive neuroepithelial tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000251	Fallopian Tube Carcinoma	skos:exactMatch	DOID:1963	fallopian tube carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000252	Fallopian Tube Carcinosarcoma	skos:exactMatch	DOID:1970	fallopian tube carcinosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000253	Fallopian Tube Serous Adenocarcinoma	skos:exactMatch	DOID:5598	fallopian tube serous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000254	Fibroadenoma	skos:exactMatch	DOID:9006947	Fibroadenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000255	Fibroblastic Neoplasm	skos:exactMatch	DOID:9008446	Fibrous Tissue Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000256	Fibrolamellar Carcinoma	skos:exactMatch	DOID:5015	fibrolamellar carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000257	Fibrous Hamartoma of Infancy	skos:exactMatch	DOID:9007066	Fibrous Hamartoma of Infancy	semapv:ManualMappingCuration	2023-12-04
EFO:1000258	Fibrous Meningioma	skos:exactMatch	DOID:7211	fibrous meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000259	Flat Urothelial Hyperplasia	skos:exactMatch	DOID:9002221	Hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000262	Gallbladder Adenocarcinoma	skos:exactMatch	DOID:3500	gallbladder adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000263	Gallbladder Adenoma	skos:exactMatch	DOID:0050893	gallbladder adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000264	Gallbladder Adenosquamous Carcinoma	skos:exactMatch	DOID:5627	adenosquamous gallbladder carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000265	Gallbladder Biliary Intraepithelial Neoplasia	skos:exactMatch	DOID:0060071	pre-malignant neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000266	Gallbladder Small Cell Neuroendocrine Carcinoma	skos:exactMatch	DOID:7133	gallbladder small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000267	Gallbladder Squamous Cell Carcinoma	skos:exactMatch	DOID:5535	gallbladder squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000269	Gastric Choriocarcinoma	skos:exactMatch	DOID:3594	choriocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000270	Gastric Diffuse Large B-Cell Lymphoma	skos:exactMatch	DOID:9007929	Gastric Diffuse Large B-Cell Lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000271	Gastric Hamartomatous Polyp	skos:exactMatch	DOID:9003987	Gastric Polyposis	semapv:ManualMappingCuration	2023-12-04
EFO:1000272	Gastric Mantle Cell Lymphoma	skos:exactMatch	DOID:0050746	mantle cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000273	Gastric Metaplasia	skos:exactMatch	DOID:9000217	Stomach Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000274	Gastric Mucosa-Associated Lymphoid Tissue Lymphoma	skos:exactMatch	DOID:9007252	Gastric Mucosa-Associated Lymphoid Tissue Lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000275	Gastric Neuroendocrine Tumor G1	skos:exactMatch	DOID:4715	gastric neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000276	Gastric Papillary Adenocarcinoma	skos:exactMatch	DOID:5593	gastric papillary adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000277	Gastric Small Cell Neuroendocrine Carcinoma	skos:exactMatch	DOID:6552	gastric small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000278	Gastric Squamous Cell Carcinoma	skos:exactMatch	DOID:5516	gastric squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000280	Gastrointestinal Hamartoma	skos:exactMatch	DOID:9007253	Hamartoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000281	Giant Cell Tumor of Soft Tissue	skos:exactMatch	DOID:9003853	Giant Cell Tumors	semapv:ManualMappingCuration	2023-12-04
EFO:1000283	Grade III Prostatic Intraepithelial Neoplasia	skos:exactMatch	DOID:8634	prostate carcinoma in situ	semapv:ManualMappingCuration	2022-01-24
EFO:1000284	Granular Cell Tumor	skos:exactMatch	DOID:2411	granular cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000285	Granular Cell Tumor of the Neurohypophysis	skos:exactMatch	DOID:5047	granular cell tumor of the sellar region	semapv:ManualMappingCuration	2022-01-24
EFO:1000286	Granulocytic Sarcoma	skos:exactMatch	DOID:9000063	Primary Granulocytic Sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000287	Growth Hormone-Producing Pituitary Gland Adenoma	skos:exactMatch	DOID:6255	growth hormone secreting pituitary adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000288	Head and Neck Paraganglioma	skos:exactMatch	DOID:9004893	Head and Neck Paraganglioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000289	Hemangiopericytic Neoplasm	skos:exactMatch	DOID:3850	hemangiopericytic tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000291	Hepatic Granuloma	skos:exactMatch	DOID:9006916	Hepatic Granuloma	semapv:ManualMappingCuration	2023-12-04
EFO:1000292	Hepatoblastoma	skos:exactMatch	DOID:687	hepatoblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000293	Hepatoid Adenocarcinoma	skos:exactMatch	DOID:0060534	hepatoid adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000294	HER2 Positive Breast Carcinoma	skos:exactMatch	DOID:0060079	Her2-receptor positive breast cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000295	Hidradenocarcinoma	skos:exactMatch	DOID:9006371	Hidradenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000296	High Grade Surface Osteosarcoma	skos:exactMatch	DOID:3374	peripheral osteosarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000297	Histiocytic and Dendritic Cell Neoplasm	skos:exactMatch	DOID:5621	histiocytic and dendritic cell cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000298	Hydatidiform Mole	skos:exactMatch	DOID:9005147	Hydatidiform Mole	semapv:ManualMappingCuration	2023-12-04
EFO:1000300	Ileal Neuroendocrine Tumor G1	skos:exactMatch	DOID:9003896	Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1000300	Ileal Neuroendocrine Tumor G1	skos:exactMatch	DOID:9004109	Intestinal Carcinoid Tumors	semapv:ManualMappingCuration	2023-12-04
EFO:1000302	Infiltrating Bladder Lymphoepithelioma-Like Carcinoma	skos:exactMatch	DOID:7600	infiltrating bladder lymphoepithelioma-like carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000303	Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant	skos:exactMatch	DOID:7553	infiltrating bladder urothelial carcinoma sarcomatoid variant	semapv:ManualMappingCuration	2022-01-24
EFO:1000304	Intestinal Type Adenocarcinoma	skos:exactMatch	DOID:9001857	Intestinal Type Adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000305	Intimal Sarcoma	skos:exactMatch	DOID:9007431	Intimal Sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000306	Intraductal Breast Papilloma	skos:exactMatch	DOID:1626	breast duct papilloma	semapv:ManualMappingCuration	2023-12-04
EFO:1000307	Invasive Breast Carcinoma	skos:exactMatch	DOID:9008344	Invasive Breast Carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000308	Jejunal Neuroendocrine Tumor G1	skos:exactMatch	DOID:4434	small intestine neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000309	Juvenile Myelomonocytic Leukemia	skos:exactMatch	DOID:0050458	juvenile myelomonocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1000310	Juvenile Polyp	skos:exactMatch	DOID:0050787	juvenile polyposis syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1000311	Juvenile Xanthogranuloma	skos:exactMatch	DOID:4424	juvenile xanthogranuloma	semapv:ManualMappingCuration	2022-01-24
EFO:1000312	Kidney Angiomyolipoma	skos:exactMatch	DOID:8411	kidney angiomyolipoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000313	Kidney Cyst	skos:exactMatch	DOID:2975	cystic kidney disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000314	Kidney Medullary Carcinoma	skos:exactMatch	DOID:0070475	SMARCB1-deficient renal medullary carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000314	Kidney Medullary Carcinoma	skos:exactMatch	DOID:4464	collecting duct carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000315	Kidney Oncocytoma	skos:exactMatch	DOID:6245	renal oncocytoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000316	Krukenberg Tumor	skos:exactMatch	DOID:9597	Krukenberg carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000317	Lacrimal Gland Adenoid Cystic Carcinoma	skos:exactMatch	DOID:4870	lacrimal gland adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000318	Langerhans Cell Histiocytosis	skos:exactMatch	DOID:2571	Langerhans-cell histiocytosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000319	Laryngeal Adenoid Cystic Carcinoma	skos:exactMatch	DOID:4869	laryngeal adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000320	Laryngeal Small Cell Carcinoma	skos:exactMatch	DOID:7144	laryngeal small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000321	Leydig Cell Tumor	skos:exactMatch	DOID:2696	Leydig cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000324	Liver Inflammatory Myofibroblastic Tumor	skos:exactMatch	DOID:918	liver inflammatory pseudotumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000326	Lobular Breast Carcinoma In Situ	skos:exactMatch	DOID:3010	lobular neoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000327	Low Grade Central Osteosarcoma	skos:exactMatch	DOID:7602	conventional osteosarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000328	Low Grade Fibromyxoid Sarcoma	skos:exactMatch	DOID:0080534	myxofibrosarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000330	Low Grade Vulvar Intraepithelial Neoplasia	skos:exactMatch	DOID:9006454	vulvar intraepithelial neoplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000332	Lung Giant Cell Carcinoma	skos:exactMatch	DOID:5583	lung giant cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000333	Lung Inflammatory Myofibroblastic Tumor	skos:exactMatch	DOID:0050905	inflammatory myofibroblastic tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000334	Lung Lymphangioleiomyomatosis	skos:exactMatch	DOID:3319	lymphangioleiomyomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000335	Lung Papilloma	skos:exactMatch	DOID:2615	papilloma	semapv:ManualMappingCuration	2023-12-04
EFO:1000336	Lung Sarcomatoid Carcinoma	skos:exactMatch	DOID:0080777	lung sarcomatoid carcinoma	semapv:ManualMappingCuration	2023-03-17
EFO:1000337	Lung Sclerosing Hemangioma	skos:exactMatch	DOID:495	sclerosing hemangioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000337	Lung Sclerosing Hemangioma	skos:exactMatch	DOID:5766	pulmonary sclerosing hemangioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000338	Lung Signet Ring Cell Carcinoma	skos:exactMatch	DOID:0080305	signet ring lung adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000339	Lymphangiosarcoma	skos:exactMatch	DOID:2689	lymphangiosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000340	Lymphoepithelioma-Like Lung Carcinoma	skos:exactMatch	DOID:4556	lung large cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000341	Lymphomatoid Papulosis	skos:exactMatch	DOID:9003867	Lymphomatoid Papulosis	semapv:ManualMappingCuration	2023-12-04
EFO:1000342	Lymphoplasmacyte-Rich Meningioma	skos:exactMatch	DOID:4591	lymphoplasmacyte-rich meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000344	Major Salivary Gland Carcinoma	skos:exactMatch	DOID:0050904	salivary gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000346	Major Salivary Gland Mucoepidermoid Carcinoma	skos:exactMatch	DOID:0081293	salivary gland mucoepidermoid carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000347	Malignancy in Giant Cell Tumor of Bone	skos:exactMatch	DOID:4719	bone giant cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000348	Malignant Adrenal Gland Pheochromocytoma	skos:exactMatch	DOID:0050892	adrenal gland pheochromocytoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000348	Malignant Adrenal Gland Pheochromocytoma	skos:exactMatch	DOID:0080347	malignant pheochromocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000349	Malignant Bladder Paraganglioma	skos:exactMatch	DOID:0050936	extra-adrenal pheochromocytoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000350	Malignant Bone Neoplasm	skos:exactMatch	DOID:184	bone cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000352	Malignant Germ Cell Tumor	skos:exactMatch	DOID:2994	germ cell cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000353	Malignant Jugulotympanic Paraganglioma	skos:exactMatch	DOID:9002449	Glomus Jugulare Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000354	Malignant Laryngeal Neoplasm	skos:exactMatch	DOID:2596	larynx cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000355	Malignant Mesothelioma	skos:exactMatch	DOID:1790	malignant mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000356	Malignant Mixed Neoplasm	skos:exactMatch	DOID:154	mixed cell type cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000356	Malignant Mixed Neoplasm	skos:exactMatch	DOID:9008713	Malignant Mixed Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000357	Malignant Ovarian Brenner Tumor	skos:exactMatch	DOID:4217	malignant ovarian Brenner tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000358	Malignant Ovarian Mixed Epithelial Tumor	skos:exactMatch	DOID:6898	ovarian seromucinous carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000359	Malignant Pancreatic Neoplasm	skos:exactMatch	DOID:1793	pancreatic cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000360	Malignant Paraganglioma	skos:exactMatch	DOID:9008757	Metastatic Paraganglioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000361	Malignant Peripheral Nerve Sheath Tumor with Mesenchymal Differentiation	skos:exactMatch	DOID:5940	malignant peripheral nerve sheath tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000362	Malignant Pleural Neoplasm	skos:exactMatch	DOID:5158	pleural cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000363	Malignant Urinary System Neoplasm	skos:exactMatch	DOID:3996	urinary system cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000364	Mast Cell Sarcoma	skos:exactMatch	DOID:355	mast-cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000365	Maxillary Sinus Adenoid Cystic Carcinoma	skos:exactMatch	DOID:7198	maxillary sinus adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000366	Mediastinal Malignant Germ Cell Tumor	skos:exactMatch	DOID:5559	mediastinal cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000367	Mediastinal Neuroblastoma	skos:exactMatch	DOID:10660	mediastinum neuroblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000368	Medullomyoblastoma with Myogenic Differentiation	skos:exactMatch	DOID:3861	medullomyoblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000369	Melanocytoma of the Eyeball	skos:exactMatch	DOID:9004059	Eye Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000370	Meningeal Melanocytoma	skos:exactMatch	DOID:5900	meningeal melanocytoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000371	Meningioangiomatosis	skos:exactMatch	DOID:9002729	Meningioangiomatosis	semapv:ManualMappingCuration	2023-12-04
EFO:1000372	Meningothelial Meningioma	skos:exactMatch	DOID:7212	meningothelial meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000373	Metanephric Adenoma	skos:exactMatch	DOID:6404	metanephric adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000375	Metaplastic Meningioma	skos:exactMatch	DOID:3565	meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000376	Microcystic Meningioma	skos:exactMatch	DOID:4594	microcystic meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000377	Micropapillary Serous Carcinoma	skos:exactMatch	DOID:2632	papillary serous adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000378	Middle Ear Squamous Cell Carcinoma	skos:exactMatch	DOID:5526	middle ear squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000379	Minor Salivary Gland Adenocarcinoma	skos:exactMatch	DOID:0050904	salivary gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000380	Mixed Cell Uveal Melanoma	skos:exactMatch	DOID:6522	mixed cell uveal melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000381	Mixed Epithelial Stromal Tumor of the Kidney	skos:exactMatch	DOID:9002265	Kidney Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000382	Mixed Lobular and Ductal Breast Carcinoma	skos:exactMatch	DOID:3458	breast adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000383	Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma	skos:exactMatch	DOID:5395	functioning pituitary adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000384	Mixed Tumor of the Salivary Gland	skos:exactMatch	DOID:452	pleomorphic adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000385	Mixed Tumor of the Skin	skos:exactMatch	DOID:2079	eccrine mixed tumor of skin	semapv:ManualMappingCuration	2022-01-24
EFO:1000386	Mucinous Gastric Adenocarcinoma	skos:exactMatch	DOID:3716	mucinous stomach adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000388	Myelodysplastic/Myeloproliferative Neoplasm	skos:exactMatch	DOID:4972	myelodysplastic/myeloproliferative neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000389	Myofibroma	skos:exactMatch	DOID:4386	myofibroma	semapv:ManualMappingCuration	2022-01-24
EFO:1000390	Nabothian Cyst	skos:exactMatch	DOID:9007583	Cysts	semapv:ManualMappingCuration	2023-12-04
EFO:1000391	Nasal Cavity Polyp	skos:exactMatch	DOID:9001472	Nasal Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1000393	Neuroblastic Tumor	skos:exactMatch	DOID:9008058	Neuroblastic Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000394	Neurothekeoma	skos:exactMatch	DOID:9000825	Neurothekeoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000395	Nevus of Ito	skos:exactMatch	DOID:3156	hypomelanosis of Ito	semapv:ManualMappingCuration	2023-12-04
EFO:1000396	Nevus of Ota	skos:exactMatch	DOID:9005777	Nevus of Ota	semapv:ManualMappingCuration	2023-12-04
EFO:1000397	Non-Cutaneous Melanoma	skos:exactMatch	DOID:1909	melanoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000399	Non-Functioning Adrenal Cortex Adenoma	skos:exactMatch	DOID:0050891	adrenal cortical adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000400	Non-Neoplastic Bile Duct Disorder	skos:exactMatch	DOID:4138	bile duct disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000401	Non-Seminomatous Lesion	skos:exactMatch	DOID:4086	testicular germ cell tumor non-seminomatous	semapv:ManualMappingCuration	2023-12-04
EFO:1000402	Normal Breast-Like Subtype of Breast Carcinoma	skos:exactMatch	DOID:3458	breast adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000403	Ocular Melanoma	skos:exactMatch	DOID:1752	ocular melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000404	Ocular Melanoma with Extraocular Extension	skos:exactMatch	DOID:1752	ocular melanoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000405	Ocular Sebaceous Carcinoma	skos:exactMatch	DOID:295	eye carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000405	Ocular Sebaceous Carcinoma	skos:exactMatch	DOID:4840	sebaceous carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000406	Odontogenic Cyst	skos:exactMatch	DOID:9002504	Odontogenic Cysts	semapv:ManualMappingCuration	2023-12-04
EFO:1000407	Olfactory Neuroblastoma	skos:exactMatch	DOID:369	olfactory neuroblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000408	Ossifying Fibromyxoid Tumor	skos:exactMatch	DOID:2685	ossifying fibromyxoid tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000409	Ossifying Renal Tumor of Infancy	skos:exactMatch	DOID:3116	kidney benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000410	Osteoblastoma	skos:exactMatch	DOID:0060098	osteoblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000411	Osteochondroma	skos:exactMatch	DOID:9005193	Osteochondroma	semapv:ManualMappingCuration	2023-12-04
EFO:1000412	Ovarian Carcinosarcoma	skos:exactMatch	DOID:6170	ovarian carcinosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000413	Ovarian Choriocarcinoma	skos:exactMatch	DOID:5550	choriocarcinoma of ovary	semapv:ManualMappingCuration	2022-01-24
EFO:1000414	Ovarian Dysgerminoma	skos:exactMatch	DOID:5511	dysgerminoma of ovary	semapv:ManualMappingCuration	2022-01-24
EFO:1000415	Ovarian Embryonal Carcinoma	skos:exactMatch	DOID:5681	ovarian embryonal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000416	Ovarian Endometrioid Adenocarcinoma	skos:exactMatch	DOID:5828	endometrioid ovary carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000417	Ovarian Endometrioid Adenocarcinoma with Squamous Differentiation	skos:exactMatch	DOID:5828	endometrioid ovary carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000418	Ovarian Endometriosis	skos:exactMatch	DOID:11432	endometriosis of ovary	semapv:ManualMappingCuration	2022-01-24
EFO:1000419	Ovarian Germ Cell Tumor	skos:exactMatch	DOID:2156	ovarian germ cell cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000420	Ovarian Gonadoblastoma	skos:exactMatch	DOID:3578	ovarian gonadoblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000421	Ovarian Granulosa Cell Tumor	skos:exactMatch	DOID:9002365	Ovarian Granulosa Cell Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000422	Ovarian Gynandroblastoma	skos:exactMatch	DOID:9008041	Ovarian Gynandroblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000423	Ovarian Leydig Cell Tumor	skos:exactMatch	DOID:2696	Leydig cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000424	Ovarian Microcystic Stromal Tumor	skos:exactMatch	DOID:0080369	ovarian sex-cord stromal tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000425	Ovarian Mixed Epithelial Tumor	skos:exactMatch	DOID:6211	mixed epithelial tumor of ovary	semapv:ManualMappingCuration	2023-12-04
EFO:1000426	Ovarian Sclerosing Stromal Tumor	skos:exactMatch	DOID:0080369	ovarian sex-cord stromal tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000427	Ovarian Serous Adenocarcinofibroma	skos:exactMatch	DOID:5744	ovary serous adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000428	Ovarian Serous Adenofibroma	skos:exactMatch	DOID:5474	ovarian serous adenofibroma	semapv:ManualMappingCuration	2022-01-24
EFO:1000429	Ovarian Sertoli-Leydig Cell Tumor	skos:exactMatch	DOID:2997	Sertoli-Leydig cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000430	Ovarian Sex Cord Tumor with Annular Tubules	skos:exactMatch	DOID:0080369	ovarian sex-cord stromal tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000431	Ovarian Small Cell Carcinoma	skos:exactMatch	DOID:6179	ovarian small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000432	Ovarian Squamous Cell Carcinoma	skos:exactMatch	DOID:5531	ovarian squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000433	Ovarian Steroid Cell Tumor	skos:exactMatch	DOID:9002762	Ovarian Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000434	Ovarian Stromal Luteoma	skos:exactMatch	DOID:7880	luteoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000435	Ovarian Transitional Cell Carcinoma	skos:exactMatch	DOID:4000	ovary transitional cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000436	Ovarian Tumor of the Thecoma/Fibroma Group	skos:exactMatch	DOID:9002762	Ovarian Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000437	Ovarian Yolk Sac Tumor	skos:exactMatch	DOID:5350	ovarian endodermal sinus tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000438	Palmar Fibromatosis	skos:exactMatch	DOID:9003793	Dupuytren Contracture	semapv:ManualMappingCuration	2023-12-04
EFO:1000439	Pancreatic Acinar Cell Carcinoma	skos:exactMatch	DOID:5742	pancreatic acinar cell adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000440	Pancreatic Gastrinoma	skos:exactMatch	DOID:5580	pancreatic gastrinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000442	Pancreatic Large Cell Neuroendocrine Carcinoma	skos:exactMatch	DOID:4905	pancreatic carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000443	Pancreatic Precancerous Condition	skos:exactMatch	DOID:0060071	pre-malignant neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000444	Pancreatic Small Cell Neuroendocrine Carcinoma	skos:exactMatch	DOID:1800	neuroendocrine carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000445	Pancreatic Vipoma	skos:exactMatch	DOID:5741	pancreatic vasoactive intestinal peptide producing tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000446	Pancreatoblastoma	skos:exactMatch	DOID:6823	pancreatoblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000447	Papillary Craniopharyngioma	skos:exactMatch	DOID:3847	papillary craniopharyngioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000448	Papillary Cystic Neoplasm	skos:exactMatch	DOID:9008105	Cystic, Mucinous, and Serous Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000449	Papillary Meningioma	skos:exactMatch	DOID:5058	rhabdoid meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000450	Papillary Transitional Cell Carcinoma	skos:exactMatch	DOID:4012	papillary transitional carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000451	Papillary Tumor of the Pineal Region	skos:exactMatch	DOID:0081251	papillary tumor of the pineal region	semapv:ManualMappingCuration	2023-12-04
EFO:1000452	Parachordoma	skos:exactMatch	DOID:2647	parachordoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000453	Paraganglioma	skos:exactMatch	DOID:0050773	paraganglioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000454	Paranasal Sinus Adenoid Cystic Carcinoma	skos:exactMatch	DOID:0050619	paranasal sinus cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000455	Paranasal Sinus Schneiderian Papilloma	skos:exactMatch	DOID:1350	paranasal sinus benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000456	Parathyroid Gland Carcinoma	skos:exactMatch	DOID:1540	parathyroid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000457	Parathyroid Hyperplasia	skos:exactMatch	DOID:9003102	Parathyroid Gland Hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000458	Parotid Gland Acinic Cell Carcinoma	skos:exactMatch	DOID:3025	acinar cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000459	Parotid Gland Adenoid Cystic Carcinoma	skos:exactMatch	DOID:0050931	parotid gland adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000460	Parotid Gland Carcinoma	skos:exactMatch	DOID:9036	parotid gland cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000461	Parotid Gland Carcinoma ex Pleomorphic Adenoma	skos:exactMatch	DOID:297	pleomorphic adenoma carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000462	Parotid Gland Pleomorphic Adenoma	skos:exactMatch	DOID:452	pleomorphic adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000463	Parotid Gland Squamous Cell Carcinoma	skos:exactMatch	DOID:9009187	Aerodigestive Tract Squamous Cell Carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000464	PEComa	skos:exactMatch	DOID:2643	perivascular epithelioid cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000465	Penile Carcinoma	skos:exactMatch	DOID:3449	penis carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000466	Penile Fibromatosis	skos:exactMatch	DOID:8616	Peyronie's disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000467	Peritoneal Mesothelioma	skos:exactMatch	DOID:1788	peritoneal mesothelioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000468	Peritoneal Multicystic Mesothelioma	skos:exactMatch	DOID:1788	peritoneal mesothelioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000469	Peritoneal Well Differentiated Papillary Mesothelioma	skos:exactMatch	DOID:1788	peritoneal mesothelioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000470	Peutz-Jeghers Polyp	skos:exactMatch	DOID:3852	Peutz-Jeghers syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1000471	Peutz-Jeghers Polyp of the Stomach	skos:exactMatch	DOID:3852	Peutz-Jeghers syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1000472	Pharyngeal Adenoid Cystic Carcinoma	skos:exactMatch	DOID:0060119	pharynx cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000473	Phosphaturic Mesenchymal Tumor	skos:exactMatch	DOID:9000313	Phosphaturic Mesenchymal Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000474	Pineal Parenchymal Tumor of Intermediate Differentiation	skos:exactMatch	DOID:5030	pineal parenchymal tumor of intermediate differentiation	semapv:ManualMappingCuration	2022-01-24
EFO:1000475	Pineoblastoma	skos:exactMatch	DOID:1664	pineoblastoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000476	Pineocytoma	skos:exactMatch	DOID:0081248	pineocytoma	semapv:ManualMappingCuration	2023-03-17
EFO:1000476	Pineocytoma	skos:exactMatch	DOID:9005957	Pinealoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000477	Pituicytoma	skos:exactMatch	DOID:0081280	pituicytoma	semapv:ManualMappingCuration	2023-04-17
EFO:1000478	Pituitary Gland Adenoma	skos:exactMatch	DOID:3829	pituitary adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000479	Placental Choriocarcinoma	skos:exactMatch	DOID:2024	placental choriocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000480	Placental Hemangioma	skos:exactMatch	DOID:277	chorioangioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000481	Plantar Fibromatosis	skos:exactMatch	DOID:8936	plantar fascial fibromatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000484	Pleural Epithelioid Mesothelioma	skos:exactMatch	DOID:4489	malignant epithelial mesothelioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000485	Pleural Mesothelioma	skos:exactMatch	DOID:5157	benign pleural mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000486	Pleural Sarcomatoid Mesothelioma	skos:exactMatch	DOID:7474	malignant pleural mesothelioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000487	Plexiform Ameloblastoma	skos:exactMatch	DOID:0050894	ameloblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000488	Polar Spongioblastoma	skos:exactMatch	DOID:7305	astroblastoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000491	Primary Effusion Lymphoma	skos:exactMatch	DOID:9000035	Primary Effusion Lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000492	Primary Intraosseous Squamous Cell Carcinoma	skos:exactMatch	DOID:9006134	Odontogenic Tumors	semapv:ManualMappingCuration	2023-12-04
EFO:1000493	Primary Melanocytic Lesion of Meninges	skos:exactMatch	DOID:5900	meningeal melanocytoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000494	Primary Peritoneal Serous Adenocarcinoma	skos:exactMatch	DOID:4901	peritoneal serous adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000495	Primary Pulmonary Diffuse Large B-Cell Lymphoma	skos:exactMatch	DOID:0050745	diffuse large B-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000496	Prolactin-Producing Pituitary Gland Adenoma	skos:exactMatch	DOID:5394	prolactinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000497	Prolactin-Producing Pituitary Gland Carcinoma	skos:exactMatch	DOID:5396	prolactin producing pituitary tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000498	Prostate Rhabdomyosarcoma	skos:exactMatch	DOID:3252	prostate rhabdomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000499	Prostate Small Cell Carcinoma	skos:exactMatch	DOID:7141	prostate small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000500	Psammomatous Meningioma	skos:exactMatch	DOID:7210	psammomatous meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000501	Pyloric Gland Adenoma	skos:exactMatch	DOID:9003987	Gastric Polyposis	semapv:ManualMappingCuration	2023-12-04
EFO:1000502	Rectal Hyperplastic Polyp	skos:exactMatch	DOID:9001642	Intestinal Polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1000503	Rectal Traditional Serrated Adenoma	skos:exactMatch	DOID:0050915	rectal adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000504	Rectal Tubular Adenoma	skos:exactMatch	DOID:0050915	rectal adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000505	Rectal Tubulovillous Adenoma	skos:exactMatch	DOID:0050915	rectal adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000506	Rectal Villous Adenoma	skos:exactMatch	DOID:0050915	rectal adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000507	Renal Angiomyoadenomatous Tumor	skos:exactMatch	DOID:3116	kidney benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000508	Renal Cell Carcinoma Associated with Xp11.2 Translocations/TFE3 Gene Fusions	skos:exactMatch	DOID:0081415	TFE3-rearranged renal cell carcinoma	semapv:ManualMappingCuration	2024-04-21
EFO:1000509	Retinal Neoplasm	skos:exactMatch	DOID:9006483	Retinal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000510	Retroperitoneal Inflammatory Myofibroblastic Tumor	skos:exactMatch	DOID:0050905	inflammatory myofibroblastic tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000511	Rhabdoid Meningioma	skos:exactMatch	DOID:5058	rhabdoid meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000512	Rhabdoid Tumor of the Kidney	skos:exactMatch	DOID:3674	kidney rhabdoid cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000513	Salivary Gland Acinic Cell Carcinoma	skos:exactMatch	DOID:3025	acinar cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000514	Salivary Gland Adenosquamous Carcinoma	skos:exactMatch	DOID:0050904	salivary gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000516	Salivary Gland Carcinoma ex Pleomorphic Adenoma	skos:exactMatch	DOID:0050904	salivary gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000516	Salivary Gland Carcinoma ex Pleomorphic Adenoma	skos:exactMatch	DOID:297	pleomorphic adenoma carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000517	Salivary Gland Large Cell Carcinoma	skos:exactMatch	DOID:0050904	salivary gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000519	Salivary Gland Small Cell Carcinoma	skos:exactMatch	DOID:0050685	small cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000520	Sarcomatoid Carcinoma	skos:exactMatch	DOID:4015	sarcomatoid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000521	Sarcomatoid Mesothelioma	skos:exactMatch	DOID:4488	sarcomatoid mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000522	Secretory Meningioma	skos:exactMatch	DOID:4588	secretory meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000523	Sex Hormone-Producing Adrenal Cortex Adenoma	skos:exactMatch	DOID:0050891	adrenal cortical adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000524	Signet Ring Cell Gastric Adenocarcinoma	skos:exactMatch	DOID:8025	gastric signet ring cell adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000525	Simple Endometrial Hyperplasia	skos:exactMatch	DOID:0080365	endometrial hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000526	Simple Endometrial Hyperplasia with Atypia	skos:exactMatch	DOID:0080365	endometrial hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000527	Sinonasal Undifferentiated Carcinoma	skos:exactMatch	DOID:0080799	sinonasal undifferentiated carcinoma	semapv:ManualMappingCuration	2023-03-17
EFO:1000529	Skin Basosquamous Cell Carcinoma	skos:exactMatch	DOID:5063	basosquamous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000530	Skin Cavernous Hemangioma	skos:exactMatch	DOID:483	cavernous hemangioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000531	Skin Sarcoma	skos:exactMatch	DOID:2687	skin sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000532	small intestinal adenocarcinoma	skos:exactMatch	DOID:4906	small intestine adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000533	Small Intestinal Burkitt Lymphoma	skos:exactMatch	DOID:8584	Burkitt lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000534	Small Intestinal Diffuse Large B-Cell Lymphoma	skos:exactMatch	DOID:0050745	diffuse large B-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000535	Small Intestinal Enteropathy-Associated T-Cell Lymphoma	skos:exactMatch	DOID:9003745	Enteropathy-Associated T-Cell Lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000536	Small Intestinal Intraepithelial Neoplasia	skos:exactMatch	DOID:0060071	pre-malignant neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000537	Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma	skos:exactMatch	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue	semapv:ManualMappingCuration	2023-12-04
EFO:1000538	Small Intestinal Tubular Adenoma	skos:exactMatch	DOID:7505	small intestine benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000539	Small Intestinal Tubulovillous Adenoma	skos:exactMatch	DOID:7505	small intestine benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000540	Soft Tissue Chondroma	skos:exactMatch	DOID:3814	soft tissue chondroma	semapv:ManualMappingCuration	2022-01-24
EFO:1000541	Soft Tissue Neoplasm	skos:exactMatch	DOID:9007429	Soft Tissue Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000542	Solid Pseudopapillary Neoplasm of the Pancreas	skos:exactMatch	DOID:9004301	Solid Pseudopapillary Neoplasm of the Pancreas	semapv:ManualMappingCuration	2023-12-04
EFO:1000543	Spinal Chordoma	skos:exactMatch	DOID:4153	spinal chordoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000544	Spinal Cord Astrocytoma	skos:exactMatch	DOID:4863	spinal cord astrocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000545	Spinal Cord Primitive Neuroectodermal Tumor	skos:exactMatch	DOID:6872	spinal cord primitive neuroectodermal neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000546	Spindle Cell Melanoma	skos:exactMatch	DOID:3162	malignant spindle cell melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000547	Splenic Diffuse Large B-Cell Lymphoma	skos:exactMatch	DOID:0050745	diffuse large B-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000548	Splenic Hodgkin Lymphoma	skos:exactMatch	DOID:8567	Hodgkin's lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000549	Splenic Mantle Cell Lymphoma	skos:exactMatch	DOID:0050746	mantle cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000550	Splenic Marginal Zone Lymphoma	skos:exactMatch	DOID:0050750	splenic marginal zone lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000551	Stromal Predominant Kidney Wilms Tumor	skos:exactMatch	DOID:5191	stromal predominant kidney Wilms' tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000552	Subcutaneous Panniculitis-Like T-Cell Lymphoma	skos:exactMatch	DOID:9008980	Subcutaneous Panniculitis-like T-Cell Lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000553	Subependymoma	skos:exactMatch	DOID:4843	subependymal glioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000554	Submandibular Gland Adenocarcinoma	skos:exactMatch	DOID:9173	submandibular gland cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000555	Submandibular Gland Adenoid Cystic Carcinoma	skos:exactMatch	DOID:9173	submandibular gland cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000556	Superficial Fibromatosis	skos:exactMatch	DOID:0050871	fibroma	semapv:ManualMappingCuration	2023-12-04
EFO:1000557	Synovial Chondromatosis	skos:exactMatch	DOID:9001695	Synovial Chondromatosis	semapv:ManualMappingCuration	2023-12-04
EFO:1000558	Syringocystadenoma Papilliferum	skos:exactMatch	DOID:5445	syringocystadenoma papilliferum	semapv:ManualMappingCuration	2022-01-24
EFO:1000559	Systemic Mastocytosis with Associated Clonal Hematological non-Mast-Cell Lineage Disease	skos:exactMatch	DOID:4797	SM-AHNMD	semapv:ManualMappingCuration	2022-01-24
EFO:1000560	T-Cell Prolymphocytic Leukemia	skos:exactMatch	DOID:0081042	T-cell prolymphocytic leukemia	semapv:ManualMappingCuration	2023-03-17
EFO:1000562	Tenosynovial Giant Cell Tumor	skos:exactMatch	DOID:314	tenosynovial giant cell tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000563	Teratoma with Malignant Transformation	skos:exactMatch	DOID:0081246	teratoma with somatic-type malignancy	semapv:ManualMappingCuration	2023-06-18
EFO:1000563	Teratoma with Malignant Transformation	skos:exactMatch	DOID:5563	malignant teratoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000564	Testicular Choriocarcinoma	skos:exactMatch	DOID:5551	choriocarcinoma of the testis	semapv:ManualMappingCuration	2022-01-24
EFO:1000565	Testicular Embryonal Carcinoma	skos:exactMatch	DOID:5680	embryonal testis carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000566	Testicular Germ Cell Tumor	skos:exactMatch	DOID:5557	testicular germ cell cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000566	Testicular Germ Cell Tumor	skos:exactMatch	DOID:9003654	Testicular Germ Cell Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000567	Testicular Granulosa Cell Tumor	skos:exactMatch	DOID:5331	testicular granulosa cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000568	Testicular Large Cell Calcifying Sertoli Cell Tumor	skos:exactMatch	DOID:3577	Sertoli cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000569	Testicular Leydig Cell Tumor	skos:exactMatch	DOID:4756	testicular Leydig cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000570	Testicular Non-Seminomatous Germ Cell Tumor	skos:exactMatch	DOID:4086	testicular germ cell tumor non-seminomatous	semapv:ManualMappingCuration	2022-01-24
EFO:1000571	Testicular Sclerosing Sertoli Cell Tumor	skos:exactMatch	DOID:3577	Sertoli cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000572	Testicular Sertoli Cell Tumor	skos:exactMatch	DOID:3577	Sertoli cell tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1000573	Testicular Teratoma	skos:exactMatch	DOID:9005592	Testicular Teratoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000574	Testicular Yolk Sac Tumor	skos:exactMatch	DOID:5344	testicular yolk sac tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000575	Therapy-Related Myeloid Neoplasm	skos:exactMatch	DOID:9001012	Therapy-Related Myeloid Neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000576	Thymic Carcinoma	skos:exactMatch	DOID:3284	thymic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000576	Thymic Carcinoma	skos:exactMatch	DOID:4554	type C thymoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000577	Thymic Sarcomatoid Carcinoma	skos:exactMatch	DOID:8138	thymus sarcomatoid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000578	Thymic Small Cell Carcinoma	skos:exactMatch	DOID:7142	thymus small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000579	Thymic Squamous Cell Carcinoma	skos:exactMatch	DOID:5530	thymus squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000580	Thymic Undifferentiated Carcinoma	skos:exactMatch	DOID:3284	thymic carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000581	Thymoma	skos:exactMatch	DOID:3275	thymoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000582	Thymoma Type AB	skos:exactMatch	DOID:3280	mixed type thymoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000583	Thymoma Type B3	skos:exactMatch	DOID:7926	epithelial malignant thymoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000584	Thymoma Type B1	skos:exactMatch	DOID:6917	predominantly cortical thymoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000585	Thyroglossal Duct Cyst	skos:exactMatch	DOID:9007559	Thyroglossal Cyst	semapv:ManualMappingCuration	2023-12-04
EFO:1000587	Thyroid Gland Diffuse Large B-Cell Lymphoma	skos:exactMatch	DOID:0050745	diffuse large B-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000588	Thyroid Gland Hyalinizing Trabecular Tumor	skos:exactMatch	DOID:6203	thyroid hyalinizing trabecular adenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000589	Thyroid Gland Mixed Medullary and Follicular Cell Carcinoma	skos:exactMatch	DOID:0081459	thyroid gland mixed medullary and follicular cell-derived carcinoma	semapv:ManualMappingCuration	2024-07-29
EFO:1000589	Thyroid Gland Mixed Medullary and Follicular Cell Carcinoma	skos:exactMatch	DOID:3963	thyroid gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000590	Thyroid Gland Mucoepidermoid Carcinoma	skos:exactMatch	DOID:4687	thyroid gland mucoepidermoid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000591	Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma	skos:exactMatch	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue	semapv:ManualMappingCuration	2023-12-04
EFO:1000592	Thyroid Gland Oncocytic Follicular Carcinoma	skos:exactMatch	DOID:8161	oncocytic carcinoma of the thyroid	semapv:ManualMappingCuration	2023-12-04
EFO:1000593	Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation	skos:exactMatch	DOID:0050923	spindle epithelial tumor with thymus-like differentiation tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000594	Thyroid Gland Squamous Cell Carcinoma	skos:exactMatch	DOID:3963	thyroid gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000595	Thyroid Gland Undifferentiated (Anaplastic) Carcinoma	skos:exactMatch	DOID:0080522	anaplastic thyroid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000596	Tibial Adamantinoma	skos:exactMatch	DOID:6322	tibial adamantinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000597	Tonsillar Squamous Cell Carcinoma	skos:exactMatch	DOID:0050920	tonsil squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
EFO:1000597	Tonsillar Squamous Cell Carcinoma	skos:exactMatch	DOID:1749	squamous cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000598	Tracheal Adenoid Cystic Carcinoma	skos:exactMatch	DOID:4875	trachea adenoid cystic carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000599	Tracheal Carcinoma	skos:exactMatch	DOID:4876	trachea carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000600	Tracheal Squamous Cell Carcinoma	skos:exactMatch	DOID:12003	trachea squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000601	Transitional Cell Carcinoma	skos:exactMatch	DOID:2671	transitional cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000602	Transitional Meningioma	skos:exactMatch	DOID:7213	transitional meningioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000603	Unclassified Renal Cell Carcinoma	skos:exactMatch	DOID:4450	renal cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000605	Undifferentiated Ovarian Carcinoma	skos:exactMatch	DOID:4001	ovarian carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000606	Undifferentiated Pancreatic Carcinoma	skos:exactMatch	DOID:3498	pancreatic ductal adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000607	Undifferentiated Pancreatic Carcinoma with Osteoclast-Like Giant Cells	skos:exactMatch	DOID:7718	osteoclast-like giant cell neoplasm of the pancreas	semapv:ManualMappingCuration	2022-01-24
EFO:1000608	Undifferentiated Pleomorphic Sarcoma, Inflammatory Variant	skos:exactMatch	DOID:6192	malignant inflammatory fibrous histiocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000609	Ureter Carcinoma	skos:exactMatch	DOID:4939	ureter carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000610	Ureter Small Cell Carcinoma	skos:exactMatch	DOID:6886	ureter small cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000611	Urothelial Dysplasia	skos:exactMatch	DOID:5433	urinary tract papillary transitional cell benign neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1000612	Usual Ductal Breast Hyperplasia	skos:exactMatch	DOID:9004693	ductal breast hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000613	Uterine Carcinosarcoma	skos:exactMatch	DOID:6171	uterine carcinosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000614	Uterine Corpus Lipoleiomyoma	skos:exactMatch	DOID:13957	uterine corpus lipoleiomyoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000616	Uveal Melanoma	skos:exactMatch	DOID:6039	uveal melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000617	Vaginal Adenoid Cystic Carcinoma	skos:exactMatch	DOID:0050918	vaginal carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000618	Vaginal Carcinosarcoma	skos:exactMatch	DOID:136	vaginal carcinosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000619	Vaginal Melanoma	skos:exactMatch	DOID:9006069	vaginal melanoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000620	Vaginal Squamous Cell Carcinoma	skos:exactMatch	DOID:0050918	vaginal carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000621	Vagus Nerve Paraganglioma	skos:exactMatch	DOID:0050773	paraganglioma	semapv:ManualMappingCuration	2023-12-04
EFO:1000622	VIP-Producing Neuroendocrine Tumor	skos:exactMatch	DOID:5574	vipoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000623	Vulvar Lichen Sclerosus	skos:exactMatch	DOID:9000555	Vulvar Lichen Sclerosus	semapv:ManualMappingCuration	2023-12-04
EFO:1000624	Vulvar Squamous Cell Carcinoma	skos:exactMatch	DOID:2101	vulva squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000625	Warthin Tumor	skos:exactMatch	DOID:9001884	Adenolymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000627	thyroid disease	skos:exactMatch	DOID:50	thyroid gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000630	marginal zone B-cell lymphoma	skos:exactMatch	DOID:0050748	marginal zone lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000631	palsy	skos:exactMatch	DOID:9005246	Paralysis	semapv:ManualMappingCuration	2023-12-04
EFO:1000632	cerebral palsy	skos:exactMatch	DOID:1969	cerebral palsy	semapv:ManualMappingCuration	2022-01-24
EFO:1000633	adenomatous colon polyp	skos:exactMatch	DOID:0050424	familial adenomatous polyposis	semapv:ManualMappingCuration	2023-12-04
EFO:1000634	hamartoma	skos:exactMatch	DOID:9007253	Hamartoma	semapv:ManualMappingCuration	2023-12-04
EFO:1000635	hemangioma	skos:exactMatch	DOID:255	hemangioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000636	inflammatory skin disease	skos:exactMatch	DOID:2723	dermatitis	semapv:ManualMappingCuration	2023-12-04
EFO:1000637	acute respiratory distress syndrome	skos:exactMatch	DOID:11394	adult respiratory distress syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1000638	Isaacs syndrome	skos:exactMatch	DOID:963	episodic ataxia	semapv:ManualMappingCuration	2022-01-24
EFO:1000639	acquired metabolic disease	skos:exactMatch	DOID:0060158	acquired metabolic disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000640	basal ganglia cerebrovascular disease	skos:exactMatch	DOID:10991	basal ganglia cerebrovascular disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000641	congenital nonspherocytic hemolytic anemia	skos:exactMatch	DOID:2861	congenital nonspherocytic hemolytic anemia	semapv:ManualMappingCuration	2022-01-24
EFO:1000642	hemochromatosis	skos:exactMatch	DOID:2352	hemochromatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000643	infantile epileptic encephalopathy	skos:exactMatch	DOID:0050709	early infantile epileptic encephalopathy	semapv:ManualMappingCuration	2023-12-04
EFO:1000644	newborn respiratory distress syndrome	skos:exactMatch	DOID:12716	newborn respiratory distress syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000645	orthostatic intolerance	skos:exactMatch	DOID:0111154	postural orthostatic tachycardia syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000645	orthostatic intolerance	skos:exactMatch	DOID:9004453	Orthostatic Intolerance	semapv:ManualMappingCuration	2023-12-04
EFO:1000646	papillary carcinoma	skos:exactMatch	DOID:3113	papillary carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000647	renal tubular transport disease	skos:exactMatch	DOID:447	renal tubular transport disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000648	developmental dysplasia of the hip	skos:exactMatch	DOID:0060930	developmental dysplasia of the hip	semapv:ManualMappingCuration	2024-04-21
EFO:1000648	developmental dysplasia of the hip	skos:exactMatch	DOID:9005560	Congenital Hip Dislocation	semapv:ManualMappingCuration	2023-12-04
EFO:1000649	estrogen-receptor positive breast cancer	skos:exactMatch	DOID:0060075	estrogen-receptor positive breast cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000650	estrogen-receptor negative breast cancer	skos:exactMatch	DOID:0060076	estrogen-receptor negative breast cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000652	acute pancreatitis	skos:exactMatch	DOID:2913	acute pancreatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000653	sarcopenia	skos:exactMatch	DOID:9008824	Sarcopenia	semapv:ManualMappingCuration	2023-12-04
EFO:1000654	childhood cancer	skos:exactMatch	DOID:162	cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1000656	sporadic Creutzfeld Jacob disease	skos:exactMatch	DOID:9000794	Sporadic Creutzfeldt-Jakob Disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000657	rectum cancer	skos:exactMatch	DOID:1993	rectum cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000660	acanthosis nigricans	skos:exactMatch	DOID:3138	acanthosis nigricans	semapv:ManualMappingCuration	2022-01-24
EFO:1000661	Achenbach syndrome	skos:exactMatch	DOID:6687	Achenbach syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000662	acneiform dermatitis	skos:exactMatch	DOID:4399	acneiform dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000663	acquired keratosis	skos:exactMatch	DOID:13072	acquired hyperkeratosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000664	acrodermatitis	skos:exactMatch	DOID:2722	acrodermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000665	acrodermatitis chronica atrophicans	skos:exactMatch	DOID:0060344	acrodermatitis chronica atrophicans	semapv:ManualMappingCuration	2022-01-24
EFO:1000666	acrokeratosis verruciformis	skos:exactMatch	DOID:0050606	acrokeratosis verruciformis	semapv:ManualMappingCuration	2022-01-24
EFO:1000667	adiposis dolorosa	skos:exactMatch	DOID:3928	adiposis dolorosa	semapv:ManualMappingCuration	2022-01-24
EFO:1000668	allergic contact dermatitis	skos:exactMatch	DOID:3042	allergic contact dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000669	allergic urticaria	skos:exactMatch	DOID:10612	allergic urticaria	semapv:ManualMappingCuration	2022-01-24
EFO:1000670	anhidrosis	skos:exactMatch	DOID:11156	anhidrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000671	bacterial exanthem	skos:exactMatch	DOID:0050487	bacterial exanthem	semapv:ManualMappingCuration	2022-01-24
EFO:1000674	carbuncle	skos:exactMatch	DOID:2176	carbuncle	semapv:ManualMappingCuration	2022-01-24
EFO:1000675	cholesteatoma	skos:exactMatch	DOID:869	cholesteatoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000676	cholesteatoma of attic	skos:exactMatch	DOID:10963	cholesteatoma of attic	semapv:ManualMappingCuration	2022-01-24
EFO:1000677	cholesteatoma of external ear	skos:exactMatch	DOID:9462	cholesteatoma of external ear	semapv:ManualMappingCuration	2022-01-24
EFO:1000678	cholesteatoma of middle ear	skos:exactMatch	DOID:10964	cholesteatoma of middle ear	semapv:ManualMappingCuration	2022-01-24
EFO:1000679	cholinergic urticaria	skos:exactMatch	DOID:14443	cholinergic urticaria	semapv:ManualMappingCuration	2022-01-24
EFO:1000680	mucous membrane pemphigoid	skos:exactMatch	DOID:11656	cicatricial pemphigoid	semapv:ManualMappingCuration	2022-01-24
EFO:1000681	congenital generalized lipodystrophy	skos:exactMatch	DOID:0050585	congenital generalized lipodystrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1000682	conjunctival pigmentation	skos:exactMatch	DOID:12304	conjunctival pigmentation	semapv:ManualMappingCuration	2022-01-24
EFO:1000683	cutaneous diphtheria	skos:exactMatch	DOID:12275	cutaneous diphtheria	semapv:ManualMappingCuration	2022-01-24
EFO:1000684	dermatitis herpetiformis	skos:exactMatch	DOID:8505	dermatitis herpetiformis	semapv:ManualMappingCuration	2022-01-24
EFO:1000685	dermatographia	skos:exactMatch	DOID:743	dermatographia	semapv:ManualMappingCuration	2022-01-24
EFO:1000686	dermatosis papulosa nigra	skos:exactMatch	DOID:4400	dermatosis papulosa nigra	semapv:ManualMappingCuration	2022-01-24
EFO:1000687	diffuse lipomatosis	skos:exactMatch	DOID:3923	diffuse lipomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000688	dyshidrosis	skos:exactMatch	DOID:9230	pompholyx	semapv:ManualMappingCuration	2022-01-24
EFO:1000689	ecthyma	skos:exactMatch	DOID:11907	ecthyma	semapv:ManualMappingCuration	2022-01-24
EFO:1000690	epidermolysis bullosa	skos:exactMatch	DOID:2730	epidermolysis bullosa	semapv:ManualMappingCuration	2022-01-24
EFO:1000691	epidermolysis bullosa acquisita	skos:exactMatch	DOID:4313	epidermolysis bullosa acquisita	semapv:ManualMappingCuration	2022-01-24
EFO:1000692	epidermolysis bullosa dystrophica	skos:exactMatch	DOID:4959	epidermolysis bullosa dystrophica	semapv:ManualMappingCuration	2022-01-24
EFO:1000693	erythema infectiosum	skos:exactMatch	DOID:8743	erythema infectiosum	semapv:ManualMappingCuration	2022-01-24
EFO:1000694	erythema multiforme	skos:exactMatch	DOID:0050185	erythema multiforme	semapv:ManualMappingCuration	2022-01-24
EFO:1000695	erythematosquamous dermatosis	skos:exactMatch	DOID:9097	erythematosquamous dermatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000696	erythrasma	skos:exactMatch	DOID:4131	erythrasma	semapv:ManualMappingCuration	2022-01-24
EFO:1000697	exanthem	skos:exactMatch	DOID:0050486	exanthem	semapv:ManualMappingCuration	2022-01-24
EFO:1000698	facial dermatosis	skos:exactMatch	DOID:3134	facial dermatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000699	fibroepithelial polyp of the anus	skos:exactMatch	DOID:8170	fibroepithelial polyp of the anus	semapv:ManualMappingCuration	2022-01-24
EFO:1000700	fibroepithelial polyp of urethra	skos:exactMatch	DOID:8108	fibroepithelial polyp of urethra	semapv:ManualMappingCuration	2022-01-24
EFO:1000701	follicular mucinosis	skos:exactMatch	DOID:9905	follicular mucinosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000702	folliculitis	skos:exactMatch	DOID:4409	folliculitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000703	fox fordyce disease	skos:exactMatch	DOID:1381	Fox-Fordyce disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000704	granuloma annulare	skos:exactMatch	DOID:3777	granuloma annulare	semapv:ManualMappingCuration	2022-01-24
EFO:1000705	granulomatous dermatitis	skos:exactMatch	DOID:4397	granulomatous dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000706	hand dermatosis	skos:exactMatch	DOID:3158	hand dermatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000707	hemangioma of subcutaneous tissue	skos:exactMatch	DOID:13081	hemangioma of subcutaneous tissue	semapv:ManualMappingCuration	2022-01-24
EFO:1000708	hereditary papulotranslucent acrokeratoderma	skos:exactMatch	DOID:0060360	hereditary papulotranslucent acrokeratoderma	semapv:ManualMappingCuration	2022-01-24
EFO:1000709	pemphigoid gestationis	skos:exactMatch	DOID:0040098	pemphigus gestationis	semapv:ManualMappingCuration	2022-01-24
EFO:1000709	pemphigoid gestationis	skos:exactMatch	DOID:14482	pemphigoid gestationis	semapv:ManualMappingCuration	2022-01-24
EFO:1000710	hidradenitis suppurativa	skos:exactMatch	DOID:2280	hidradenitis suppurativa	semapv:ManualMappingCuration	2022-01-24
EFO:1000710	hidradenitis suppurativa	skos:exactMatch	DOID:2282	hidradenitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000711	hyperpigmentation of eyelid	skos:exactMatch	DOID:10122	hyperpigmentation of eyelid	semapv:ManualMappingCuration	2022-01-24
EFO:1000712	hypohidrosis	skos:exactMatch	DOID:11155	hypohidrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000713	hypopigmentation of eyelid	skos:exactMatch	DOID:11668	hypopigmentation of eyelid	semapv:ManualMappingCuration	2022-01-24
EFO:1000714	impetigo	skos:exactMatch	DOID:8504	impetigo	semapv:ManualMappingCuration	2022-01-24
EFO:1000715	impetigo herpetiformis	skos:exactMatch	DOID:8503	impetigo herpetiformis	semapv:ManualMappingCuration	2022-01-24
EFO:1000717	inverted follicular keratosis	skos:exactMatch	DOID:6945	inverted follicular keratosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000718	irritant dermatitis	skos:exactMatch	DOID:2772	irritant dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000719	juvenile dermatitis herpetiformis	skos:exactMatch	DOID:8507	juvenile dermatitis herpetiformis	semapv:ManualMappingCuration	2022-01-24
EFO:1000720	keratosis	skos:exactMatch	DOID:161	keratosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000721	kernicterus due to isoimmunization	skos:exactMatch	DOID:12043	kernicterus due to isoimmunization	semapv:ManualMappingCuration	2022-01-24
EFO:1000722	Kimura disease	skos:exactMatch	DOID:7365	Kimura disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000723	leg dermatosis	skos:exactMatch	DOID:3142	leg dermatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000724	lichen disease	skos:exactMatch	DOID:8574	lichen disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000725	lichen nitidus	skos:exactMatch	DOID:8573	lichen nitidus	semapv:ManualMappingCuration	2022-01-24
EFO:1000726	lichen planus	skos:exactMatch	DOID:9201	lichen planus	semapv:ManualMappingCuration	2022-01-24
EFO:1000727	lipodystrophy	skos:exactMatch	DOID:811	lipodystrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1000728	lipomatosis	skos:exactMatch	DOID:3153	lipomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000729	loiasis	skos:exactMatch	DOID:13523	loiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1000730	Ludwig's angina	skos:exactMatch	DOID:4558	Ludwig's angina	semapv:ManualMappingCuration	2022-01-24
EFO:1000731	maxillary sinus cholesteatoma	skos:exactMatch	DOID:867	maxillary sinus cholesteatoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000732	mediastinal lipomatosis	skos:exactMatch	DOID:3926	mediastinal lipomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000733	melanoacanthoma	skos:exactMatch	DOID:11684	melanoacanthoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000734	miliaria	skos:exactMatch	DOID:1382	miliaria	semapv:ManualMappingCuration	2022-01-24
EFO:1000735	miliaria rubra	skos:exactMatch	DOID:11153	miliaria rubra	semapv:ManualMappingCuration	2022-01-24
EFO:1000736	mongolian spot	skos:exactMatch	DOID:4702	mongolian spot	semapv:ManualMappingCuration	2022-01-24
EFO:1000737	multiple symmetric lipomatosis	skos:exactMatch	DOID:14116	multiple symmetric lipomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000738	necrobiosis lipoidica	skos:exactMatch	DOID:3486	necrobiosis lipoidica	semapv:ManualMappingCuration	2022-01-24
EFO:1000739	neonatal jaundice	skos:exactMatch	DOID:2383	neonatal jaundice	semapv:ManualMappingCuration	2022-01-24
EFO:1000740	neurodermatitis	skos:exactMatch	DOID:3309	neurodermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000741	neurotic excoriation	skos:exactMatch	DOID:9165	neurotic excoriation	semapv:ManualMappingCuration	2022-01-24
EFO:1000742	nodular nonsuppurative panniculitis	skos:exactMatch	DOID:1525	nodular nonsuppurative panniculitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000744	occupational dermatitis	skos:exactMatch	DOID:4404	occupational dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000745	palmoplantar keratosis	skos:exactMatch	DOID:3390	palmoplantar keratosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000746	panniculitis	skos:exactMatch	DOID:1526	panniculitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000747	parapsoriasis	skos:exactMatch	DOID:9088	parapsoriasis	semapv:ManualMappingCuration	2022-01-24
EFO:1000748	pelvic lipomatosis	skos:exactMatch	DOID:3927	pelvic lipomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000749	pemphigus	skos:exactMatch	DOID:9182	pemphigus	semapv:ManualMappingCuration	2022-01-24
EFO:1000750	perinatal jaundice due to hepatocellular damage	skos:exactMatch	DOID:11452	perinatal jaundice due to hepatocellular damage	semapv:ManualMappingCuration	2022-01-24
EFO:1000752	photosensitivity disease	skos:exactMatch	DOID:3159	photosensitivity disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000753	phototoxic dermatitis	skos:exactMatch	DOID:3818	photoallergic dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000753	phototoxic dermatitis	skos:exactMatch	DOID:4407	phototoxic dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000754	physical urticaria	skos:exactMatch	DOID:0060220	physical urticaria	semapv:ManualMappingCuration	2022-01-24
EFO:1000755	pigmentation disease	skos:exactMatch	DOID:10123	pigmentation disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000756	pityriasis rosea	skos:exactMatch	DOID:8892	pityriasis rosea	semapv:ManualMappingCuration	2022-01-24
EFO:1000757	porokeratosis	skos:exactMatch	DOID:3805	porokeratosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000758	punctate palmoplantar keratoderma type III	skos:exactMatch	DOID:0060362	punctate palmoplantar keratoderma type III	semapv:ManualMappingCuration	2022-01-24
EFO:1000759	reactive cutaneous fibrous lesion	skos:exactMatch	DOID:2053	reactive cutaneous fibrous lesion	semapv:ManualMappingCuration	2022-01-24
EFO:1000760	rosacea	skos:exactMatch	DOID:8881	rosacea	semapv:ManualMappingCuration	2022-01-24
EFO:1000761	scalp dermatosis	skos:exactMatch	DOID:3136	scalp dermatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000762	scleredema adultorum	skos:exactMatch	DOID:3140	scleredema adultorum	semapv:ManualMappingCuration	2022-01-24
EFO:1000763	sebaceous gland disease	skos:exactMatch	DOID:9098	sebaceous gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000764	seborrheic dermatitis	skos:exactMatch	DOID:8741	seborrheic dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000765	seborrheic infantile dermatitis	skos:exactMatch	DOID:8941	seborrheic infantile dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000766	skin atrophy	skos:exactMatch	DOID:2733	skin atrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1000767	skin sarcoidosis	skos:exactMatch	DOID:13402	skin sarcoidosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000768	spongiotic dermatitis	skos:exactMatch	DOID:4406	spongiotic dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000769	steroid lipomatosis	skos:exactMatch	DOID:3925	steroid lipomatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000770	stromal corneal pigmentation	skos:exactMatch	DOID:12311	stromal corneal pigmentation	semapv:ManualMappingCuration	2022-01-24
EFO:1000771	subcorneal pustular dermatosis	skos:exactMatch	DOID:8508	subcorneal pustular dermatosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000772	sweat gland disease	skos:exactMatch	DOID:1383	sweat gland disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000773	toxicodendron dermatitis	skos:exactMatch	DOID:3819	toxicodendron dermatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000774	vesiculobullous skin disease	skos:exactMatch	DOID:2731	vesiculobullous skin disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000775	vibratory urticaria	skos:exactMatch	DOID:1554	vibratory urticaria	semapv:ManualMappingCuration	2022-01-24
EFO:1000776	viral exanthem	skos:exactMatch	DOID:8672	viral exanthem	semapv:ManualMappingCuration	2022-01-24
EFO:1000777	vulva fibroepithelial polyp	skos:exactMatch	DOID:8255	vulva fibroepithelial polyp	semapv:ManualMappingCuration	2022-01-24
EFO:1000778	vulvar inverted follicular keratosis	skos:exactMatch	DOID:6943	vulvar inverted follicular keratosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000779	vulvar seborrheic keratosis	skos:exactMatch	DOID:6944	vulvar seborrheic keratosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000780	autoimmune pancreatitis type 1	skos:exactMatch	DOID:0040091	autoimmune pancreatitis	semapv:ManualMappingCuration	2023-12-04
EFO:1000781	overactive bladder	skos:exactMatch	DOID:0070355	overactive bladder syndrome	semapv:ManualMappingCuration	2023-04-17
EFO:1000782	altitude sickness	skos:exactMatch	DOID:9005785	Altitude Sickness	semapv:ManualMappingCuration	2023-12-04
EFO:1000783	diabetic neuropathy	skos:exactMatch	DOID:11503	diabetic autonomic neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000783	diabetic neuropathy	skos:exactMatch	DOID:12785	diabetic polyneuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000783	diabetic neuropathy	skos:exactMatch	DOID:9743	diabetic neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000784	microscopic polyangiitis	skos:exactMatch	DOID:9005070	Microscopic Polyangiitis	semapv:ManualMappingCuration	2023-12-04
EFO:1000785	Sezary's disease	skos:exactMatch	DOID:8541	Sezary's disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000786	osteoarthritis, hip	skos:exactMatch	DOID:9006041	Osteoarthritis, Hip	semapv:ManualMappingCuration	2023-12-04
EFO:1000787	osteoarthritis, spine	skos:exactMatch	DOID:9005882	Spine Osteoarthritis	semapv:ManualMappingCuration	2023-12-04
EFO:1000788	osteoarthritis, toe	skos:exactMatch	DOID:8398	osteoarthritis	semapv:ManualMappingCuration	2023-12-04
EFO:1000789	osteoarthritis, hand	skos:exactMatch	DOID:9005040	Hand Osteoarthritis	semapv:ManualMappingCuration	2023-12-04
EFO:1000790	acalculous cholecystitis	skos:exactMatch	DOID:2828	acalculous cholecystitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000791	acidophil adenoma	skos:exactMatch	DOID:5392	acidophil adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000792	Acinetobacter infectious disease	skos:exactMatch	DOID:3091	Acinetobacter infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000793	Actinobacillus infectious disease	skos:exactMatch	DOID:9007041	Actinobacillus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000794	acute kidney tubular necrosis	skos:exactMatch	DOID:12556	acute kidney tubular necrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000795	acute retinal necrosis syndrome	skos:exactMatch	DOID:3611	acute retinal necrosis syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000796	adrenal cortex carcinoma	skos:exactMatch	DOID:3948	adrenocortical carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000796	adrenal cortex carcinoma	skos:exactMatch	DOID:3959	adrenal cortical adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000796	adrenal cortex carcinoma	skos:exactMatch	DOID:660	adrenal cortex cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000797	adrenal gland hyperfunction	skos:exactMatch	DOID:3947	adrenal gland hyperfunction	semapv:ManualMappingCuration	2022-01-24
EFO:1000798	adrenal rest tumor	skos:exactMatch	DOID:1786	adrenal rest tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000799	afferent loop syndrome	skos:exactMatch	DOID:8438	afferent loop syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000800	alcohol withdrawal delirium	skos:exactMatch	DOID:9001129	Alcohol Withdrawal Delirium	semapv:ManualMappingCuration	2023-12-04
EFO:1000801	alcoholic cardiomyopathy	skos:exactMatch	DOID:12935	alcoholic cardiomyopathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000802	alcoholic liver cirrhosis	skos:exactMatch	DOID:14018	alcoholic liver cirrhosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000803	alcoholic neuropathy	skos:exactMatch	DOID:14183	alcoholic neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000804	anal gland neoplasm	skos:exactMatch	DOID:4550	anal gland neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000805	angioid streaks	skos:exactMatch	DOID:13401	angioid streaks	semapv:ManualMappingCuration	2022-01-24
EFO:1000806	angiomyoma	skos:exactMatch	DOID:4265	angiomyoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000807	anterior cerebral artery infarction	skos:exactMatch	DOID:3528	anterior cerebral artery infarction	semapv:ManualMappingCuration	2022-01-24
EFO:1000808	anterior compartment syndrome	skos:exactMatch	DOID:3933	anterior compartment syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000809	anterior ischemic optic neuropathy	skos:exactMatch	DOID:12010	anterior ischemic optic neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000810	anterior spinal artery syndrome	skos:exactMatch	DOID:6712	anterior spinal artery syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000811	anterior uveitis	skos:exactMatch	DOID:1407	anterior uveitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000812	anterolateral myocardial infarction	skos:exactMatch	DOID:5845	anterolateral myocardial infarction	semapv:ManualMappingCuration	2022-01-24
EFO:1000813	anthracosilicosis	skos:exactMatch	DOID:10324	anthracosilicosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000814	anthracosis	skos:exactMatch	DOID:10327	anthracosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000815	aortic valve prolapse	skos:exactMatch	DOID:5232	aortic valve prolapse	semapv:ManualMappingCuration	2022-01-24
EFO:1000816	aortitis	skos:exactMatch	DOID:519	aortitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000817	apparent mineralocorticoid excess syndrome	skos:exactMatch	DOID:4367	apparent mineralocorticoid excess syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000818	arcus senilis	skos:exactMatch	DOID:11342	arcus senilis	semapv:ManualMappingCuration	2022-01-24
EFO:1000819	arteriolosclerosis	skos:exactMatch	DOID:5162	arteriolosclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000820	arteriosclerosis obliterans	skos:exactMatch	DOID:5160	arteriosclerosis obliterans	semapv:ManualMappingCuration	2022-01-24
EFO:1000821	arthus reaction	skos:exactMatch	DOID:1556	arthus reaction	semapv:ManualMappingCuration	2022-01-24
EFO:1000822	ascorbic acid deficiency	skos:exactMatch	DOID:9003737	Ascorbic Acid Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1000823	aseptic meningitis	skos:exactMatch	DOID:12157	aseptic meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000824	asphyxia neonatorum	skos:exactMatch	DOID:11088	asphyxia neonatorum	semapv:ManualMappingCuration	2022-01-24
EFO:1000825	atrial heart septal defect	skos:exactMatch	DOID:1882	atrial heart septal defect	semapv:ManualMappingCuration	2022-01-24
EFO:1000826	atrophic gastritis	skos:exactMatch	DOID:8929	atrophic gastritis	semapv:ManualMappingCuration	2022-01-24
EFO:1000828	B- and T-cell mixed leukemia	skos:exactMatch	DOID:9953	acute biphenotypic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1000829	bacterial conjunctivitis	skos:exactMatch	DOID:9700	bacterial conjunctivitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000830	bacterial endocarditis	skos:exactMatch	DOID:9006552	Bacterial Endocarditis	semapv:ManualMappingCuration	2023-12-04
EFO:1000831	bacterial meningitis	skos:exactMatch	DOID:9470	bacterial meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000832	Bacteroides infectious disease	skos:exactMatch	DOID:9005284	Bacteroides Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000833	balanitis	skos:exactMatch	DOID:13033	balanitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000834	basophil adenoma	skos:exactMatch	DOID:4542	basophil adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000835	benign fibrous mesothelioma	skos:exactMatch	DOID:2653	benign fibrous mesothelioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000836	benign monoclonal gammopathy	skos:exactMatch	DOID:7442	monoclonal gammopathy of uncertain significance	semapv:ManualMappingCuration	2023-12-04
EFO:1000837	beriberi	skos:exactMatch	DOID:0070313	thiamine deficiency disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000837	beriberi	skos:exactMatch	DOID:13725	beriberi	semapv:ManualMappingCuration	2022-01-24
EFO:1000838	bile reflux	skos:exactMatch	DOID:12237	bile reflux	semapv:ManualMappingCuration	2022-01-24
EFO:1000839	bladder calculus	skos:exactMatch	DOID:11355	bladder calculus	semapv:ManualMappingCuration	2022-01-24
EFO:1000840	bladder neck obstruction	skos:exactMatch	DOID:13948	bladder neck obstruction	semapv:ManualMappingCuration	2022-01-24
EFO:1000841	blue nevus	skos:exactMatch	DOID:9001740	Blue Nevus	semapv:ManualMappingCuration	2023-12-04
EFO:1000842	Borrelia infectious disease	skos:exactMatch	DOID:9004477	Borrelia Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000843	brachial plexus neuritis	skos:exactMatch	DOID:3689	brachial plexus neuritis	semapv:ManualMappingCuration	2022-01-24
EFO:1000844	brachial plexus neuropathy	skos:exactMatch	DOID:3690	brachial plexus neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000845	brain edema	skos:exactMatch	DOID:4724	brain edema	semapv:ManualMappingCuration	2022-01-24
EFO:1000846	brain hypoxia-Ischemia	skos:exactMatch	DOID:9003676	Brain Hypoxia-Ischemia	semapv:ManualMappingCuration	2023-12-04
EFO:1000847	brain stem infarction	skos:exactMatch	DOID:3523	brain stem infarction	semapv:ManualMappingCuration	2022-01-24
EFO:1000848	breast cyst	skos:exactMatch	DOID:10350	breast cyst	semapv:ManualMappingCuration	2022-01-24
EFO:1000849	bronchial neoplasm	skos:exactMatch	DOID:3906	bronchial benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000849	bronchial neoplasm	skos:exactMatch	DOID:9001241	Bronchial Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000850	burning mouth syndrome	skos:exactMatch	DOID:4331	burning mouth syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000851	byssinosis	skos:exactMatch	DOID:10323	byssinosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000852	carcinoid syndrome	skos:exactMatch	DOID:9005598	Malignant Carcinoid Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1000853	carotid artery thrombosis	skos:exactMatch	DOID:3410	carotid artery thrombosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000854	causalgia	skos:exactMatch	DOID:3222	causalgia	semapv:ManualMappingCuration	2022-01-24
EFO:1000855	central core myopathy	skos:exactMatch	DOID:3529	congenital myopathy 1A	semapv:ManualMappingCuration	2022-01-24
EFO:1000856	central neurocytoma	skos:exactMatch	DOID:14174	central neurocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000857	central pontine myelinolysis	skos:exactMatch	DOID:636	central pontine myelinolysis	semapv:ManualMappingCuration	2022-01-24
EFO:1000858	cerebellum cancer	skos:exactMatch	DOID:4205	cerebellum cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000859	cerebral arterial disease	skos:exactMatch	DOID:3527	cerebral arterial disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000860	cerebral atherosclerosis	skos:exactMatch	DOID:12720	cerebral atherosclerosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000861	cervical rib syndrome	skos:exactMatch	DOID:9004134	Cervical Rib Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1000862	cervix erosion	skos:exactMatch	DOID:3456	cervix erosion	semapv:ManualMappingCuration	2022-01-24
EFO:1000863	Chlamydophila infectious disease	skos:exactMatch	DOID:9008527	Chlamydophila Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000864	cholecystolithiasis	skos:exactMatch	DOID:11151	cholecystolithiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1000865	choledocholithiasis	skos:exactMatch	DOID:11755	choledocholithiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1000866	choroid cancer	skos:exactMatch	DOID:12759	choroid cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000867	chromophobe adenoma	skos:exactMatch	DOID:3828	chromophobe adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000868	chronic inflammatory demyelinating polyradiculoneuropathy	skos:exactMatch	DOID:5213	chronic inflammatory demyelinating polyradiculoneuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000869	chronic interstitial cystitis	skos:exactMatch	DOID:1678	chronic interstitial cystitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000870	CNS demyelinating autoimmune disease	skos:exactMatch	DOID:9007010	Demyelinating Autoimmune Diseases, CNS	semapv:ManualMappingCuration	2023-12-04
EFO:1000871	colonic pseudo-obstruction	skos:exactMatch	DOID:3876	colonic pseudo-obstruction	semapv:ManualMappingCuration	2022-01-24
EFO:1000872	commensal Bacteroidaceae infectious disease	skos:exactMatch	DOID:9002529	Bacteroidaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000873	commensal Bifidobacteriales infectious disease	skos:exactMatch	DOID:9006887	Bifidobacteriales Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000874	commensal Clostridium infectious disease	skos:exactMatch	DOID:9006732	Clostridium Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000875	commensal Desulfovibrionaceae infectious disease	skos:exactMatch	DOID:9000464	Desulfovibrionaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000876	common bile duct neoplasm	skos:exactMatch	DOID:4608	common bile duct neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000877	complex partial epilepsy	skos:exactMatch	DOID:12382	complex partial epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:1000878	constrictive pericarditis	skos:exactMatch	DOID:11481	constrictive pericarditis	semapv:ManualMappingCuration	2022-01-24
EFO:1000879	corneal edema	skos:exactMatch	DOID:11030	corneal edema	semapv:ManualMappingCuration	2022-01-24
EFO:1000880	corneal neovascularization	skos:exactMatch	DOID:11382	corneal neovascularization	semapv:ManualMappingCuration	2022-01-24
EFO:1000881	coronary aneurysm	skos:exactMatch	DOID:3362	coronary aneurysm	semapv:ManualMappingCuration	2022-01-24
EFO:1000883	coronary thrombosis	skos:exactMatch	DOID:11847	coronary thrombosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000884	cranial nerve malignant neoplasm	skos:exactMatch	DOID:2815	cranial nerve malignant neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000885	cutaneous fibrous histiocytoma	skos:exactMatch	DOID:4418	cutaneous fibrous histiocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000886	cutaneous mastocytosis	skos:exactMatch	DOID:3663	cutaneous mastocytosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000887	cutaneous syphilis	skos:exactMatch	DOID:9008437	Cutaneous Syphilis	semapv:ManualMappingCuration	2023-12-04
EFO:1000888	cystic lymphangioma	skos:exactMatch	DOID:3081	cystic lymphangioma	semapv:ManualMappingCuration	2022-01-24
EFO:1000889	cystic, mucinous, and serous neoplasm	skos:exactMatch	DOID:9008105	Cystic, Mucinous, and Serous Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000890	Dandy-Walker syndrome	skos:exactMatch	DOID:2785	Dandy-Walker syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000891	De Quervain disease	skos:exactMatch	DOID:14107	De Quervain disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000892	dental fluorosis	skos:exactMatch	DOID:13711	dental fluorosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000893	denture stomatitis	skos:exactMatch	DOID:11875	denture stomatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000894	dermoid cyst	skos:exactMatch	DOID:2658	dermoid cyst	semapv:ManualMappingCuration	2022-01-24
EFO:1000895	desmoplastic small round cell tumor	skos:exactMatch	DOID:6785	desmoplastic small round cell tumor	semapv:ManualMappingCuration	2023-03-17
EFO:1000896	diabetic angiopathy	skos:exactMatch	DOID:11713	diabetic angiopathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000897	diabetic ketoacidosis	skos:exactMatch	DOID:1837	diabetic ketoacidosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000898	diaphragmatic eventration	skos:exactMatch	DOID:10480	diaphragmatic eventration	semapv:ManualMappingCuration	2022-01-24
EFO:1000899	diastolic heart failure	skos:exactMatch	DOID:9775	diastolic heart failure	semapv:ManualMappingCuration	2022-01-24
EFO:1000900	discitis	skos:exactMatch	DOID:10986	discitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000901	discrete subaortic stenosis	skos:exactMatch	DOID:5804	discrete subaortic stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000902	drug psychosis	skos:exactMatch	DOID:1742	drug psychosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000903	drug-induced akathisia	skos:exactMatch	DOID:9000054	Drug-Induced Akathisia	semapv:ManualMappingCuration	2023-12-04
EFO:1000904	drug-Induced dyskinesia	skos:exactMatch	DOID:9008394	Drug-Induced Dyskinesia	semapv:ManualMappingCuration	2023-12-04
EFO:1000905	drug-induced hepatitis	skos:exactMatch	DOID:2044	drug-induced hepatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000906	dry eye syndrome	skos:exactMatch	DOID:10140	dry eye syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000906	dry eye syndrome	skos:exactMatch	DOID:12895	keratoconjunctivitis sicca	semapv:ManualMappingCuration	2022-01-24
EFO:1000907	duodenal benign neoplasm	skos:exactMatch	DOID:1737	duodenal benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000908	duodenal obstruction	skos:exactMatch	DOID:3558	duodenal obstruction	semapv:ManualMappingCuration	2022-01-24
EFO:1000909	duodenogastric reflux	skos:exactMatch	DOID:4071	duodenogastric reflux	semapv:ManualMappingCuration	2022-01-24
EFO:1000910	dysplasia of cervix	skos:exactMatch	DOID:9006096	Uterine Cervical Dysplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000911	dystocia	skos:exactMatch	DOID:9008893	Dystocia	semapv:ManualMappingCuration	2023-12-04
EFO:1000912	eccrine acrospiroma	skos:exactMatch	DOID:5442	eccrine acrospiroma	semapv:ManualMappingCuration	2022-01-24
EFO:1000913	ehrlich tumor carcinoma	skos:exactMatch	DOID:5050	Ehrlich tumor carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000914	empty sella syndrome	skos:exactMatch	DOID:3642	empty sella syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000915	encephalomalacia	skos:exactMatch	DOID:2034	encephalomalacia	semapv:ManualMappingCuration	2022-01-24
EFO:1000916	endemic goiter	skos:exactMatch	DOID:13198	endemic goiter	semapv:ManualMappingCuration	2022-01-24
EFO:1000917	endocrine tuberculosis	skos:exactMatch	DOID:9000477	Endocrine Tuberculosis	semapv:ManualMappingCuration	2023-12-04
EFO:1000918	endolymphatic hydrops	skos:exactMatch	DOID:9848	endolymphatic hydrops	semapv:ManualMappingCuration	2022-01-24
EFO:1000919	endometrial stromal sarcoma	skos:exactMatch	DOID:4226	endometrial stromal sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000920	endometrial stromal tumor	skos:exactMatch	DOID:5166	endometrial stromal tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1000921	endomyocardial fibrosis	skos:exactMatch	DOID:12932	endomyocardial fibrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000922	enterotoxemia	skos:exactMatch	DOID:9006622	Enterotoxemia	semapv:ManualMappingCuration	2023-12-04
EFO:1000923	epidural neoplasm	skos:exactMatch	DOID:3618	epidural spinal canal neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000924	epilepsia partialis continua	skos:exactMatch	DOID:9006076	Epilepsia Partialis Continua	semapv:ManualMappingCuration	2023-12-04
EFO:1000925	epithelioid and spindle cell nevus	skos:exactMatch	DOID:9001326	Nevus, Epithelioid and Spindle Cell	semapv:ManualMappingCuration	2023-12-04
EFO:1000926	Erdheim-Chester disease	skos:exactMatch	DOID:4329	Erdheim-Chester disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000928	Erysipelothrix rhusiopathiae infectious disease	skos:exactMatch	DOID:0050061	erysipeloid	semapv:ManualMappingCuration	2023-03-06
EFO:1000929	Escherichia coli meningitis	skos:exactMatch	DOID:9000889	Escherichia Coli Meningitis	semapv:ManualMappingCuration	2023-12-04
EFO:1000930	esophageal diverticulosis	skos:exactMatch	DOID:13185	esophageal diverticulosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000931	euthyroid sick syndrome	skos:exactMatch	DOID:2856	euthyroid sick syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000932	extracutaneous mastocytoma	skos:exactMatch	DOID:4659	extracutaneous mastocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000933	extrahepatic cholestasis	skos:exactMatch	DOID:13619	extrahepatic cholestasis	semapv:ManualMappingCuration	2022-01-24
EFO:1000934	eyelid neoplasm	skos:exactMatch	DOID:2173	eyelid benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000935	female genital tuberculosis	skos:exactMatch	DOID:9001409	Female Genital Tuberculosis	semapv:ManualMappingCuration	2023-12-04
EFO:1000936	femoral neuropathy	skos:exactMatch	DOID:4196	femoral neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000937	fetal erythroblastosis	skos:exactMatch	DOID:1098	hemolytic disease of the fetus	semapv:ManualMappingCuration	2022-01-24
EFO:1000938	fibromuscular dysplasia	skos:exactMatch	DOID:9003785	Fibromuscular Dysplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1000939	freemartinism	skos:exactMatch	DOID:4671	freemartinism	semapv:ManualMappingCuration	2022-01-24
EFO:1000940	Frey Syndrome	skos:exactMatch	DOID:11599	Frey syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000941	frozen shoulder	skos:exactMatch	DOID:14188	frozen shoulder	semapv:ManualMappingCuration	2022-01-24
EFO:1000942	fungal meningitis	skos:exactMatch	DOID:11608	fungal meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000943	Fusobacterium infectious disease	skos:exactMatch	DOID:9001724	Fusobacterium Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000944	gait apraxia	skos:exactMatch	DOID:4260	gait apraxia	semapv:ManualMappingCuration	2022-01-24
EFO:1000945	gastric antral vascular ectasia	skos:exactMatch	DOID:2493	gastric antral vascular ectasia	semapv:ManualMappingCuration	2022-01-24
EFO:1000946	gastric mucosal hypertrophy	skos:exactMatch	DOID:8757	gastric mucosal hypertrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1000947	gastric outlet obstruction	skos:exactMatch	DOID:3122	gastric outlet obstruction	semapv:ManualMappingCuration	2022-01-24
EFO:1000948	gastroparesis	skos:exactMatch	DOID:11914	gastroparesis	semapv:ManualMappingCuration	2022-01-24
EFO:1000949	gastroschisis	skos:exactMatch	DOID:11044	gastroschisis	semapv:ManualMappingCuration	2022-01-24
EFO:1000950	giant cell reparative granuloma	skos:exactMatch	DOID:1866	giant cell reparative granuloma	semapv:ManualMappingCuration	2022-01-24
EFO:1000951	glossitis	skos:exactMatch	DOID:1456	glossitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000952	glycogen storage disease VIII	skos:exactMatch	DOID:2751	glycogen storage disease VIII	semapv:ManualMappingCuration	2022-01-24
EFO:1000953	gonadal tissue neoplasm	skos:exactMatch	DOID:9005959	Gonadal Tissue Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000954	habitual abortion	skos:exactMatch	DOID:9007479	Habitual Abortions	semapv:ManualMappingCuration	2023-12-04
EFO:1000955	Haemophilus influenzae meningitis	skos:exactMatch	DOID:0080179	haemophilus meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000956	hairy cell leukemia	skos:exactMatch	DOID:285	hairy cell leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1000957	hairy tongue	skos:exactMatch	DOID:13500	hairy tongue	semapv:ManualMappingCuration	2022-01-24
EFO:1000958	halo nevus	skos:exactMatch	DOID:9002577	Halo Nevus	semapv:ManualMappingCuration	2023-12-04
EFO:1000959	heart aneurysm	skos:exactMatch	DOID:9768	heart aneurysm	semapv:ManualMappingCuration	2022-01-24
EFO:1000960	heartwater disease	skos:exactMatch	DOID:9006636	Heartwater Disease	semapv:ManualMappingCuration	2023-12-04
EFO:1000961	Helicobacter pylori infectious disease	skos:exactMatch	DOID:9008114	Helicobacter Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1000962	hemometra	skos:exactMatch	DOID:9958	hemometra	semapv:ManualMappingCuration	2022-01-24
EFO:1000963	hemopneumothorax	skos:exactMatch	DOID:2718	hemopneumothorax	semapv:ManualMappingCuration	2022-01-24
EFO:1000964	hemorrhagic disease of newborn	skos:exactMatch	DOID:11249	vitamin K deficiency bleeding	semapv:ManualMappingCuration	2023-12-04
EFO:1000965	Henoch-Schoenlein purpura	skos:exactMatch	DOID:11123	Henoch-Schoenlein purpura	semapv:ManualMappingCuration	2022-01-24
EFO:1000966	hepatic vein thrombosis	skos:exactMatch	DOID:11512	Budd-Chiari syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000967	hidrocystoma	skos:exactMatch	DOID:3893	hidrocystoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000968	hydrophthalmos	skos:exactMatch	DOID:11212	hydrophthalmos	semapv:ManualMappingCuration	2022-01-24
EFO:1000969	hyperamylasemia	skos:exactMatch	DOID:9001176	Hyperamylasemia	semapv:ManualMappingCuration	2023-12-04
EFO:1000970	hypercementosis	skos:exactMatch	DOID:12733	hypercementosis	semapv:ManualMappingCuration	2022-01-24
EFO:1000971	hyperemesis gravidarum	skos:exactMatch	DOID:9007105	Hyperemesis Gravidarum	semapv:ManualMappingCuration	2023-12-04
EFO:1000972	hyperglobulinemic purpura	skos:exactMatch	DOID:3325	hyperglobulinemic purpura	semapv:ManualMappingCuration	2022-01-24
EFO:1000973	hyperpituitarism	skos:exactMatch	DOID:2444	hyperpituitarism	semapv:ManualMappingCuration	2022-01-24
EFO:1000974	hypersensitivity vasculitis	skos:exactMatch	DOID:9809	hypersensitivity vasculitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000975	hypersplenism	skos:exactMatch	DOID:6376	hypersplenism	semapv:ManualMappingCuration	2022-01-24
EFO:1000976	hypertensive encephalopathy	skos:exactMatch	DOID:9427	hypertensive encephalopathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000977	hypertensive retinopathy	skos:exactMatch	DOID:11561	hypertensive retinopathy	semapv:ManualMappingCuration	2022-01-24
EFO:1000978	hypervitaminosis A	skos:exactMatch	DOID:9972	hypervitaminosis A	semapv:ManualMappingCuration	2022-01-24
EFO:1000979	hypothalamic neoplasm	skos:exactMatch	DOID:3644	hypothalamic neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000980	ideomotor apraxia	skos:exactMatch	DOID:4627	ideomotor apraxia	semapv:ManualMappingCuration	2022-01-24
EFO:1000981	ileal neoplasm	skos:exactMatch	DOID:10156	benign ileal neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000981	ileal neoplasm	skos:exactMatch	DOID:9000670	Ileal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1000982	inappropriate ADH syndrome	skos:exactMatch	DOID:3401	inappropriate ADH syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000983	inferior myocardial infarction	skos:exactMatch	DOID:5850	inferior myocardial infarction	semapv:ManualMappingCuration	2022-01-24
EFO:1000984	inflammatory breast carcinoma	skos:exactMatch	DOID:6263	inflammatory breast carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1000985	intermediate coronary syndrome	skos:exactMatch	DOID:8805	intermediate coronary syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1000986	intermediate uveitis	skos:exactMatch	DOID:12732	intermediate uveitis	semapv:ManualMappingCuration	2022-01-24
EFO:1000987	intestinal perforation	skos:exactMatch	DOID:2074	intestinal perforation	semapv:ManualMappingCuration	2022-01-24
EFO:1000988	intestinal pseudo-obstruction	skos:exactMatch	DOID:0080072	intestinal pseudo-obstruction	semapv:ManualMappingCuration	2023-12-04
EFO:1000989	intestinal volvulus	skos:exactMatch	DOID:8445	intestinal volvulus	semapv:ManualMappingCuration	2022-01-24
EFO:1000990	intracranial arterial disease	skos:exactMatch	DOID:13089	intracranial arterial disease	semapv:ManualMappingCuration	2022-01-24
EFO:1000991	intracranial embolism	skos:exactMatch	DOID:4372	intracranial embolism	semapv:ManualMappingCuration	2022-01-24
EFO:1000992	intracranial hypertension	skos:exactMatch	DOID:9428	intracranial hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:1000993	intracranial hypotension	skos:exactMatch	DOID:4723	intracranial hypotension	semapv:ManualMappingCuration	2022-01-24
EFO:1000994	intracranial vasospasm	skos:exactMatch	DOID:13100	intracranial vasospasm	semapv:ManualMappingCuration	2022-01-24
EFO:1000995	intradermal nevus	skos:exactMatch	DOID:9004405	Intradermal Nevus	semapv:ManualMappingCuration	2023-12-04
EFO:1000996	iris cancer	skos:exactMatch	DOID:3478	iris cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000997	iritis	skos:exactMatch	DOID:1406	iritis	semapv:ManualMappingCuration	2022-01-24
EFO:1000998	jejunal cancer	skos:exactMatch	DOID:13499	jejunal cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1000999	joint disease	skos:exactMatch	DOID:381	arthropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001000	juxtacortical osteosarcoma	skos:exactMatch	DOID:3373	parosteal osteosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001002	kernicterus	skos:exactMatch	DOID:2382	kernicterus	semapv:ManualMappingCuration	2022-01-24
EFO:1001003	kidney cortex necrosis	skos:exactMatch	DOID:2973	kidney cortex necrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001004	kidney papillary necrosis	skos:exactMatch	DOID:2981	kidney papillary necrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001005	Klatskin's tumor	skos:exactMatch	DOID:4927	Klatskin's tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1001006	Klinefelter's syndrome	skos:exactMatch	DOID:1921	Klinefelter syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001007	krebs 2 carcinoma	skos:exactMatch	DOID:9004780	Carcinoma, Krebs 2	semapv:ManualMappingCuration	2023-12-04
EFO:1001008	kuru	skos:exactMatch	DOID:648	kuru	semapv:ManualMappingCuration	2022-01-24
EFO:1001009	kwashiorkor	skos:exactMatch	DOID:13579	kwashiorkor	semapv:ManualMappingCuration	2022-01-24
EFO:1001010	Landau-Kleffner syndrome	skos:exactMatch	DOID:2538	Landau-Kleffner syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001011	lateral medullary syndrome	skos:exactMatch	DOID:3522	lateral medullary syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001012	leptomeningeal metastasis	skos:exactMatch	DOID:9001673	leptomeningeal metastasis	semapv:ManualMappingCuration	2023-12-04
EFO:1001013	lethal midline granuloma	skos:exactMatch	DOID:9072	lethal midline granuloma	semapv:ManualMappingCuration	2022-01-24
EFO:1001014	leukemoid reaction	skos:exactMatch	DOID:9000933	Leukemoid Reaction	semapv:ManualMappingCuration	2023-12-04
EFO:1001015	leukoplakia of penis	skos:exactMatch	DOID:8738	leukoplakia of penis	semapv:ManualMappingCuration	2022-01-24
EFO:1001016	leukostasis	skos:exactMatch	DOID:12986	leukostasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001017	limited scleroderma	skos:exactMatch	DOID:1577	limited scleroderma	semapv:ManualMappingCuration	2022-01-24
EFO:1001018	lingual goiter	skos:exactMatch	DOID:13196	lingual goiter	semapv:ManualMappingCuration	2022-01-24
EFO:1001019	lip cancer	skos:exactMatch	DOID:8564	lip cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1001020	lipoid nephrosis	skos:exactMatch	DOID:10966	lipoid nephrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001021	Listeria meningitis	skos:exactMatch	DOID:11572	listeria meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001022	low tension glaucoma	skos:exactMatch	DOID:13544	low tension glaucoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001023	lupus vulgaris	skos:exactMatch	DOID:9006490	Lupus Vulgaris	semapv:ManualMappingCuration	2023-12-04
EFO:1001024	Lutembacher's syndrome	skos:exactMatch	DOID:1998	Lutembacher's syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001025	lymphangiectasis	skos:exactMatch	DOID:9002335	Lymphangiectasis	semapv:ManualMappingCuration	2023-12-04
EFO:1001026	lymphangioendothelioma	skos:exactMatch	DOID:1475	lymphangioma	semapv:ManualMappingCuration	2023-12-04
EFO:1001027	lymphangiomyoma	skos:exactMatch	DOID:9007091	Lymphangiomyoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001028	macular holes	skos:exactMatch	DOID:7633	macular holes	semapv:ManualMappingCuration	2022-01-24
EFO:1001029	magnesium deficiency	skos:exactMatch	DOID:0060879	primary hypomagnesemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001030	male genital tuberculosis	skos:exactMatch	DOID:9002028	Tuberculosis, Male Genital	semapv:ManualMappingCuration	2023-12-04
EFO:1001031	malignant hypertension	skos:exactMatch	DOID:10824	malignant hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:1001032	malignant lymphatic vessel tumor	skos:exactMatch	DOID:9003008	Lymphatic Vessel Tumors	semapv:ManualMappingCuration	2023-12-04
EFO:1001033	marasmus	skos:exactMatch	DOID:12328	marasmus	semapv:ManualMappingCuration	2022-01-24
EFO:1001034	mastitis	skos:exactMatch	DOID:10690	mastitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001035	maxillary sinus neoplasm	skos:exactMatch	DOID:1358	maxillary sinus benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001035	maxillary sinus neoplasm	skos:exactMatch	DOID:9001615	Maxillary Sinus Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001036	Meckel's diverticulum	skos:exactMatch	DOID:9487	Meckel's diverticulum	semapv:ManualMappingCuration	2022-01-24
EFO:1001037	meconium aspiration syndrome	skos:exactMatch	DOID:11049	meconium aspiration syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001038	melanotic neuroectodermal tumor	skos:exactMatch	DOID:166	melanotic neuroectodermal tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1001039	Melkersson-Rosenthal syndrome	skos:exactMatch	DOID:1761	Melkersson-Rosenthal syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001040	meningococcal meningitis	skos:exactMatch	DOID:0080176	meningococcal meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001041	mesenchymal chondrosarcoma	skos:exactMatch	DOID:4545	mesenchymal chondrosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001042	mesenchymoma	skos:exactMatch	DOID:2668	mesenchymoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001043	mesenteric vascular occlusion	skos:exactMatch	DOID:13252	mesenteric vascular occlusion	semapv:ManualMappingCuration	2022-01-24
EFO:1001044	mesothelial neoplasm	skos:exactMatch	DOID:9002899	Mesothelial Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001045	middle cerebral artery infarction	skos:exactMatch	DOID:3525	middle cerebral artery infarction	semapv:ManualMappingCuration	2022-01-24
EFO:1001047	mouth disease	skos:exactMatch	DOID:403	mouth disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001048	mucinous cystadenoma	skos:exactMatch	DOID:9000558	Mucinous Cystadenoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001050	multiple system atrophy	skos:exactMatch	DOID:4752	multiple system atrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1001051	mycosis fungoides	skos:exactMatch	DOID:8691	mycosis fungoides	semapv:ManualMappingCuration	2022-01-24
EFO:1001052	myeloid sarcoma	skos:exactMatch	DOID:8683	myeloid sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001053	myoclonic cerebellar dyssynergia	skos:exactMatch	DOID:12707	myoclonic cerebellar dyssynergia	semapv:ManualMappingCuration	2022-01-24
EFO:1001054	myofascial pain syndrome	skos:exactMatch	DOID:431	myofascial pain syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001055	myxedema	skos:exactMatch	DOID:11634	myxedema	semapv:ManualMappingCuration	2022-01-24
EFO:1001056	myxosarcoma	skos:exactMatch	DOID:4136	myxosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001057	necrotizing sialometaplasia	skos:exactMatch	DOID:12901	necrotizing sialometaplasia	semapv:ManualMappingCuration	2022-01-24
EFO:1001058	necrotizing ulcerative gingivitis	skos:exactMatch	DOID:13924	necrotizing ulcerative gingivitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001059	neonatal myasthenia gravis	skos:exactMatch	DOID:14043	neonatal myasthenia gravis	semapv:ManualMappingCuration	2022-01-24
EFO:1001060	neovascular glaucoma	skos:exactMatch	DOID:1687	neovascular glaucoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001061	neurogenic bowel	skos:exactMatch	DOID:13419	neurogenic bowel	semapv:ManualMappingCuration	2022-01-24
EFO:1001062	nodular goiter	skos:exactMatch	DOID:13197	nodular goiter	semapv:ManualMappingCuration	2022-01-24
EFO:1001063	noma	skos:exactMatch	DOID:9672	noma	semapv:ManualMappingCuration	2022-01-24
EFO:1001064	non-gestational choriocarcinoma	skos:exactMatch	DOID:4320	non-gestational choriocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001065	normal pressure hydrocephalus	skos:exactMatch	DOID:1572	normal pressure hydrocephalus	semapv:ManualMappingCuration	2022-01-24
EFO:1001066	nut allergic reaction	skos:exactMatch	DOID:4379	nut allergy	semapv:ManualMappingCuration	2022-01-24
EFO:1001067	nutritional deficiency disease	skos:exactMatch	DOID:5113	nutritional deficiency disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001068	obstructive jaundice	skos:exactMatch	DOID:13603	obstructive jaundice	semapv:ManualMappingCuration	2022-01-24
EFO:1001069	ocular hypertension	skos:exactMatch	DOID:9282	ocular hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:1001070	ocular tuberculosis	skos:exactMatch	DOID:0070344	ocular tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001071	oophoritis	skos:exactMatch	DOID:10974	oophoritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001072	opportunistic Moraxellaceae infectious disease	skos:exactMatch	DOID:9005227	Moraxellaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001073	optic nerve neoplasm	skos:exactMatch	DOID:3419	optic nerve neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001074	optic papillitis	skos:exactMatch	DOID:10175	optic papillitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001075	oral leukoedema	skos:exactMatch	DOID:4557	oral leukoedema	semapv:ManualMappingCuration	2022-01-24
EFO:1001076	orbital cellulitis	skos:exactMatch	DOID:11234	orbital cellulitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001077	orbital plasma cell granuloma	skos:exactMatch	DOID:9369	orbital plasma cell granuloma	semapv:ManualMappingCuration	2022-01-24
EFO:1001078	orchitis	skos:exactMatch	DOID:2518	orchitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001079	oxyphilic adenoma	skos:exactMatch	DOID:5389	oxyphilic adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001080	Pancoast tumor	skos:exactMatch	DOID:8007	Pancoast tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1001081	panophthalmitis	skos:exactMatch	DOID:13732	panophthalmitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001082	panuveitis	skos:exactMatch	DOID:12030	panuveitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001083	papillary follicular thyroid adenocarcinoma	skos:exactMatch	DOID:3968	papillary follicular thyroid adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001084	parametritis	skos:exactMatch	DOID:1260	parametritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001085	paraneoplastic polyneuropathy	skos:exactMatch	DOID:8681	paraneoplastic polyneuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001086	paraphimosis	skos:exactMatch	DOID:5334	paraphimosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001087	parathyroid adenoma	skos:exactMatch	DOID:7608	parathyroid adenoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001088	pars planitis	skos:exactMatch	DOID:12731	pars planitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001089	partial motor epilepsy	skos:exactMatch	DOID:3327	partial motor epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:1001090	partial sensory epilepsy	skos:exactMatch	DOID:3330	partial sensory epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:1001091	Pasteurella hemorrhagic septicemia	skos:exactMatch	DOID:9007724	Hemorrhagic Septicemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001092	patellofemoral pain syndrome	skos:exactMatch	DOID:14284	patellofemoral pain syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001093	Pelger-Huet anomaly	skos:exactMatch	DOID:9631	Pelger-Huet anomaly	semapv:ManualMappingCuration	2022-01-24
EFO:1001094	penile neoplasm	skos:exactMatch	DOID:11624	penile benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001094	penile neoplasm	skos:exactMatch	DOID:9003196	Penile Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001095	peptic esophagitis	skos:exactMatch	DOID:13976	peptic esophagitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001096	periapical granuloma	skos:exactMatch	DOID:4617	periapical granuloma	semapv:ManualMappingCuration	2022-01-24
EFO:1001097	periarthritis	skos:exactMatch	DOID:2964	periarthritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001098	pericoronitis	skos:exactMatch	DOID:3671	pericoronitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001099	perinephritis	skos:exactMatch	DOID:2982	perinephritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001100	peritoneal neoplasm	skos:exactMatch	DOID:9001834	Peritoneal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001101	periventricular leukomalacia	skos:exactMatch	DOID:13088	periventricular leukomalacia	semapv:ManualMappingCuration	2022-01-24
EFO:1001102	peroneal nerve paralysis	skos:exactMatch	DOID:6925	peroneal nerve paralysis	semapv:ManualMappingCuration	2022-01-24
EFO:1001103	persistent fetal circulation syndrome	skos:exactMatch	DOID:13042	persistent fetal circulation syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001104	phimosis	skos:exactMatch	DOID:2712	phimosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001105	pigmented spindle cell nevus	skos:exactMatch	DOID:9007860	Spindle Cell Nevus	semapv:ManualMappingCuration	2023-12-04
EFO:1001106	pigmented villonodular synovitis	skos:exactMatch	DOID:2702	pigmented villonodular synovitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001107	pilar sheath acanthoma	skos:exactMatch	DOID:4322	pilar sheath acanthoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001108	pituitary apoplexy	skos:exactMatch	DOID:1129	pituitary apoplexy	semapv:ManualMappingCuration	2022-01-24
EFO:1001109	pituitary dwarfism	skos:exactMatch	DOID:0060870	isolated growth hormone deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1001110	pituitary-dependent Cushing's disease	skos:exactMatch	DOID:3946	pituitary-dependent Cushing's disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001111	placental site trophoblastic tumor	skos:exactMatch	DOID:3596	placental site trophoblastic tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1001112	platelet storage pool deficiency	skos:exactMatch	DOID:2223	platelet storage pool deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:1001113	pneumatosis cystoides intestinalis	skos:exactMatch	DOID:13249	pneumatosis cystoides intestinalis	semapv:ManualMappingCuration	2022-01-24
EFO:1001114	pneumococcal meningitis	skos:exactMatch	DOID:9000113	Pneumococcal Meningitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001115	POEMS syndrome	skos:exactMatch	DOID:14039	POEMS syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001116	polyradiculoneuropathy	skos:exactMatch	DOID:4308	polyradiculoneuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001117	postcholecystectomy syndrome	skos:exactMatch	DOID:9740	postcholecystectomy syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001118	posterior cerebral artery infarction	skos:exactMatch	DOID:3821	posterior cerebral artery infarction	semapv:ManualMappingCuration	2022-01-24
EFO:1001119	posterior uveitis	skos:exactMatch	DOID:12574	posterior uveitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001120	potassium deficiency	skos:exactMatch	DOID:9005267	Potassium Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1001121	prediabetes syndrome	skos:exactMatch	DOID:11716	prediabetes syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001122	primary Actinomycetales infectious disease	skos:exactMatch	DOID:9000673	Actinomycetales Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001123	primary Anaplasmataceae infectious disease	skos:exactMatch	DOID:9008029	Anaplasmataceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001124	primary Bacillaceae infectious disease	skos:exactMatch	DOID:9004154	Bacillaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001125	primary Bartonellaceae infectious disease	skos:exactMatch	DOID:9003175	Bartonellaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001126	primary Fusobacteriaceae infectious disease	skos:exactMatch	DOID:9006349	Fusobacteriaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001127	primary Haemophilus infectious disease	skos:exactMatch	DOID:9000109	Haemophilus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001128	Rickettsiaceae infectious disease	skos:exactMatch	DOID:9000458	Rickettsiaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001129	proliferative vitreoretinopathy	skos:exactMatch	DOID:9719	neovascular inflammatory vitreoretinopathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001130	Proteus infectious disease	skos:exactMatch	DOID:9000517	Proteus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001131	pseudobulbar palsy	skos:exactMatch	DOID:12680	pseudobulbar palsy	semapv:ManualMappingCuration	2022-01-24
EFO:1001132	pseudotumor cerebri	skos:exactMatch	DOID:11459	pseudotumor cerebri	semapv:ManualMappingCuration	2022-01-24
EFO:1001133	pulmonary coin lesion	skos:exactMatch	DOID:5364	pulmonary coin lesion	semapv:ManualMappingCuration	2022-01-24
EFO:1001134	pulmonary edema	skos:exactMatch	DOID:11396	pulmonary edema	semapv:ManualMappingCuration	2022-01-24
EFO:1001135	pulmonary plasma cell granuloma	skos:exactMatch	DOID:3677	pulmonary plasma cell granuloma	semapv:ManualMappingCuration	2022-01-24
EFO:1001137	pulmonary subvalvular stenosis	skos:exactMatch	DOID:8861	pulmonary subvalvular stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001138	pulmonary valve stenosis	skos:exactMatch	DOID:6420	pulmonary valve stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001139	pulpitis	skos:exactMatch	DOID:11121	pulpitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001140	pyelitis	skos:exactMatch	DOID:2744	pyelitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001141	pyelonephritis	skos:exactMatch	DOID:11400	pyelonephritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001142	pyruvate carboxylase deficiency disease	skos:exactMatch	DOID:3651	pyruvate carboxylase deficiency disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001143	radial nerve lesion	skos:exactMatch	DOID:12170	radial nerve lesion	semapv:ManualMappingCuration	2022-01-24
EFO:1001144	rat-bite fever	skos:exactMatch	DOID:12096	sodoku disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001145	Raynaud disease	skos:exactMatch	DOID:10300	Raynaud disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001146	reflex epilepsy	skos:exactMatch	DOID:2548	reflex epilepsy	semapv:ManualMappingCuration	2022-01-24
EFO:1001147	reflex sympathetic dystrophy	skos:exactMatch	DOID:1811	reflex sympathetic dystrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1001148	relapsing polychondritis	skos:exactMatch	DOID:2556	relapsing polychondritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001149	renal aminoaciduria	skos:exactMatch	DOID:9002207	Renal Aminoacidurias	semapv:ManualMappingCuration	2023-12-04
EFO:1001150	renal artery obstruction	skos:exactMatch	DOID:2972	renal artery obstruction	semapv:ManualMappingCuration	2022-01-24
EFO:1001151	renal glycosuria	skos:exactMatch	DOID:9432	renal glycosuria	semapv:ManualMappingCuration	2022-01-24
EFO:1001152	renal osteodystrophy	skos:exactMatch	DOID:13068	renal osteodystrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1001153	renovascular hypertension	skos:exactMatch	DOID:1591	renovascular hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:1001154	retinal artery occlusion	skos:exactMatch	DOID:8483	retinal artery occlusion	semapv:ManualMappingCuration	2022-01-24
EFO:1001155	retinal drusen	skos:exactMatch	DOID:2569	retinal drusen	semapv:ManualMappingCuration	2022-01-24
EFO:1001156	retinal vasculitis	skos:exactMatch	DOID:11563	retinal vasculitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001157	retinal vein occlusion	skos:exactMatch	DOID:1727	retinal vein occlusion	semapv:ManualMappingCuration	2022-01-24
EFO:1001158	retinopathy of prematurity	skos:exactMatch	DOID:13025	retinopathy of prematurity	semapv:ManualMappingCuration	2022-01-24
EFO:1001159	Rh isoimmunization	skos:exactMatch	DOID:4175	Rh isoimmunization	semapv:ManualMappingCuration	2022-01-24
EFO:1001160	rheumatic fever	skos:exactMatch	DOID:1586	rheumatic fever	semapv:ManualMappingCuration	2022-01-24
EFO:1001161	rheumatic heart disease	skos:exactMatch	DOID:0050827	rheumatic heart disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001162	rickettsiosis	skos:exactMatch	DOID:9007347	Rickettsia Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001163	root caries	skos:exactMatch	DOID:14089	root caries	semapv:ManualMappingCuration	2022-01-24
EFO:1001164	SAPHO syndrome	skos:exactMatch	DOID:13677	SAPHO syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001165	Schnitzler syndrome	skos:exactMatch	DOID:4371	Schnitzler syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001166	sciatic neuropathy	skos:exactMatch	DOID:11446	sciatic neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001167	scimitar syndrome	skos:exactMatch	DOID:4297	scimitar syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001168	scrapie	skos:exactMatch	DOID:5434	scrapie	semapv:ManualMappingCuration	2022-01-24
EFO:1001169	scurvy	skos:exactMatch	DOID:13724	scurvy	semapv:ManualMappingCuration	2022-01-24
EFO:1001171	sebaceous adenocarcinoma	skos:exactMatch	DOID:4839	sebaceous adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001171	sebaceous adenocarcinoma	skos:exactMatch	DOID:4840	sebaceous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001172	sebaceous gland neoplasm	skos:exactMatch	DOID:5759	sebaceous gland neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001173	secondary hyperparathyroidism	skos:exactMatch	DOID:12466	secondary hyperparathyroidism	semapv:ManualMappingCuration	2022-01-24
EFO:1001174	secondary hypertrophic osteoarthropathy	skos:exactMatch	DOID:10393	secondary hypertrophic osteoarthropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001175	secondary Parkinson disease	skos:exactMatch	DOID:13548	secondary Parkinson disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001176	sensorineural hearing loss	skos:exactMatch	DOID:10003	sensorineural hearing loss	semapv:ManualMappingCuration	2022-01-24
EFO:1001177	septic abortion	skos:exactMatch	DOID:9003743	Septic Abortions	semapv:ManualMappingCuration	2023-12-04
EFO:1001178	shoulder impingement syndrome	skos:exactMatch	DOID:14276	shoulder impingement syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001179	sialadenitis	skos:exactMatch	DOID:10303	sialadenitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001180	sialolithiasis	skos:exactMatch	DOID:12905	sialolithiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001181	sigmoid neoplasm	skos:exactMatch	DOID:1896	sigmoid neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001182	silo filler's disease	skos:exactMatch	DOID:4374	Silo filler's disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001183	skin appendage carcinoma	skos:exactMatch	DOID:9004395	Skin Appendage Carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001184	small cell sarcoma	skos:exactMatch	DOID:3098	small cell sarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001185	smooth muscle tumor	skos:exactMatch	DOID:4310	smooth muscle tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1001186	Sneddon syndrome	skos:exactMatch	DOID:13096	Sneddon syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001187	somatostatinoma	skos:exactMatch	DOID:4430	somatostatinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001188	space motion sickness	skos:exactMatch	DOID:4796	space motion sickness	semapv:ManualMappingCuration	2022-01-24
EFO:1001189	spermatocele	skos:exactMatch	DOID:11997	spermatocele	semapv:ManualMappingCuration	2022-01-24
EFO:1001190	splenic infarction	skos:exactMatch	DOID:2533	splenic infarction	semapv:ManualMappingCuration	2022-01-24
EFO:1001191	steatitis	skos:exactMatch	DOID:9008875	Steatitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001192	struma ovarii	skos:exactMatch	DOID:2640	struma ovarii	semapv:ManualMappingCuration	2022-01-24
EFO:1001193	subacute bacterial endocarditis	skos:exactMatch	DOID:4562	subacute bacterial endocarditis	semapv:ManualMappingCuration	2022-01-24
EFO:1001194	subacute thyroiditis	skos:exactMatch	DOID:7165	subacute thyroiditis	semapv:ManualMappingCuration	2022-01-24
EFO:1001195	subclavian steal syndrome	skos:exactMatch	DOID:13002	subclavian steal syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001196	subdural empyema	skos:exactMatch	DOID:11389	subdural empyema	semapv:ManualMappingCuration	2022-01-24
EFO:1001197	subependymal glioma	skos:exactMatch	DOID:4843	subependymal glioma	semapv:ManualMappingCuration	2022-01-24
EFO:1001198	substernal goiter	skos:exactMatch	DOID:13200	substernal goiter	semapv:ManualMappingCuration	2022-01-24
EFO:1001199	subvalvular aortic stenosis	skos:exactMatch	DOID:5805	subvalvular aortic stenosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001200	sulfhemoglobinemia	skos:exactMatch	DOID:12451	sulfhemoglobinemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001201	superior mesenteric artery syndrome	skos:exactMatch	DOID:3557	superior mesenteric artery syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001202	suppurative periapical periodontitis	skos:exactMatch	DOID:2562	suppurative periapical periodontitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001203	suppurative uveitis	skos:exactMatch	DOID:13140	suppurative uveitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001204	sweat gland neoplasm	skos:exactMatch	DOID:2664	sweat gland benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001204	sweat gland neoplasm	skos:exactMatch	DOID:9007274	Sweat Gland Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001205	sympathetic ophthalmia	skos:exactMatch	DOID:12029	sympathetic ophthalmia	semapv:ManualMappingCuration	2022-01-24
EFO:1001206	syphilitic aortitis	skos:exactMatch	DOID:9880	cardiovascular syphilis	semapv:ManualMappingCuration	2023-12-04
EFO:1001207	systolic heart failure	skos:exactMatch	DOID:9651	systolic heart failure	semapv:ManualMappingCuration	2022-01-24
EFO:1001208	tarsal tunnel syndrome	skos:exactMatch	DOID:12526	tarsal tunnel syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001209	temporal arteritis	skos:exactMatch	DOID:13375	temporal arteritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001210	tethered spinal cord syndrome	skos:exactMatch	DOID:1089	tethered spinal cord syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001211	thromboangiitis obliterans	skos:exactMatch	DOID:12918	thromboangiitis obliterans	semapv:ManualMappingCuration	2022-01-24
EFO:1001212	thyroid crisis	skos:exactMatch	DOID:12837	thyroid crisis	semapv:ManualMappingCuration	2022-01-24
EFO:1001213	tibial neuropathy	skos:exactMatch	DOID:1187	tibial neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001214	tonsil cancer	skos:exactMatch	DOID:8858	tonsil cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1001216	tooth disease	skos:exactMatch	DOID:1091	tooth disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001217	Treponema infectious disease	skos:exactMatch	DOID:9000746	Treponemal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001218	tricuspid valve prolapse	skos:exactMatch	DOID:5644	tricuspid valve prolapse	semapv:ManualMappingCuration	2022-01-24
EFO:1001219	trigeminal neuralgia	skos:exactMatch	DOID:12098	trigeminal neuralgia	semapv:ManualMappingCuration	2022-01-24
EFO:1001220	trochlear nerve disease	skos:exactMatch	DOID:13864	trochlear nerve disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001221	twin-to-twin transfusion syndrome	skos:exactMatch	DOID:13576	twin-to-twin transfusion syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001222	type III hypersensitivity reaction disease	skos:exactMatch	DOID:1557	hypersensitivity reaction type III disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001223	ulcerative proctosigmoiditis	skos:exactMatch	DOID:9001164	Proctocolitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001224	ulnar neuropathy	skos:exactMatch	DOID:4613	ulnar neuropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001225	Ureaplasma urealyticum urethritis	skos:exactMatch	DOID:9005461	Ureaplasma Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001226	uremia	skos:exactMatch	DOID:4676	uremia	semapv:ManualMappingCuration	2022-01-24
EFO:1001227	ureterocele	skos:exactMatch	DOID:4022	ureterocele	semapv:ManualMappingCuration	2022-01-24
EFO:1001228	ureterolithiasis	skos:exactMatch	DOID:14146	ureterolithiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001229	maculopapular cutaneous mastocytosis	skos:exactMatch	DOID:12309	urticaria pigmentosa	semapv:ManualMappingCuration	2022-01-24
EFO:1001230	uveal cancer	skos:exactMatch	DOID:3479	uveal cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1001231	uveitis	skos:exactMatch	DOID:13141	uveitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001232	uveoparotid fever	skos:exactMatch	DOID:13404	uveoparotid fever	semapv:ManualMappingCuration	2022-01-24
EFO:1001233	variant Creutzfeldt-Jakob disease	skos:exactMatch	DOID:5435	variant Creutzfeldt-Jakob disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001234	vasculogenic impotence	skos:exactMatch	DOID:4762	vasculogenic impotence	semapv:ManualMappingCuration	2022-01-24
EFO:1001235	Vibrio infectious disease	skos:exactMatch	DOID:9001564	Vibrio Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001236	viral meningitis	skos:exactMatch	DOID:10310	viral meningitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001237	vitamin A deficiency	skos:exactMatch	DOID:9008550	Vitamin A Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1001238	vitreous detachment	skos:exactMatch	DOID:9726	vitreous detachment	semapv:ManualMappingCuration	2022-01-24
EFO:1001239	vulvitis	skos:exactMatch	DOID:3901	vulvitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001240	vulvovaginitis	skos:exactMatch	DOID:2273	vulvovaginitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001241	Wernicke encephalopathy	skos:exactMatch	DOID:2384	Wernicke encephalopathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001242	Wernicke-Korsakoff syndrome	skos:exactMatch	DOID:10915	Wernicke-Korsakoff syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001243	wheat allergic reaction	skos:exactMatch	DOID:3660	wheat allergy	semapv:ManualMappingCuration	2022-01-24
EFO:1001244	xanthogranulomatous pyelonephritis	skos:exactMatch	DOID:11401	xanthogranulomatous pyelonephritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001245	Yersinia infectious disease	skos:exactMatch	DOID:9003800	Yersinia Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001246	Yersinia pseudotuberculosis infectious disease	skos:exactMatch	DOID:9008584	Yersinia Pseudotuberculosis Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001247	chancre	skos:exactMatch	DOID:4166	syphilis	semapv:ManualMappingCuration	2023-12-04
EFO:1001248	non-alcoholic fatty liver	skos:exactMatch	DOID:0080546	non-alcoholic fatty liver	semapv:ManualMappingCuration	2023-12-04
EFO:1001249	non-alcoholic steatohepatitis	skos:exactMatch	DOID:0080547	metabolic dysfunction-associated steatohepatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001250	rotator cuff tear	skos:exactMatch	DOID:9002224	Rotator Cuff Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:1001252	gastric cardia carcinoma	skos:exactMatch	DOID:6270	gastric cardia carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001254	noise-induced hearing loss	skos:exactMatch	DOID:9002910	Hearing Loss, Noise-Induced	semapv:ManualMappingCuration	2023-12-04
EFO:1001255	spontaneous abortion	skos:exactMatch	DOID:9003281	Spontaneous Abortions	semapv:ManualMappingCuration	2023-12-04
EFO:1001256	ACTH Syndrome, Ectopic	skos:exactMatch	DOID:9001173	ACTH Syndrome, Ectopic	semapv:ManualMappingCuration	2023-12-04
EFO:1001257	acute erythroblastic leukemia	skos:exactMatch	DOID:0080916	erythroleukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001258	Adenomatosis, Pulmonary	skos:exactMatch	DOID:9001602	Pulmonary Adenomatosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001259	Adenoviridae Infections	skos:exactMatch	DOID:9000873	Adenoviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001260	alcoholic psychosis	skos:exactMatch	DOID:252	alcoholic psychosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001261	Alien Hand Syndrome	skos:exactMatch	DOID:9001656	Alien Hand Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001262	Alternariosis	skos:exactMatch	DOID:9000401	Alternariosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001263	amniotic fluid embolism	skos:exactMatch	DOID:9006155	Amniotic Fluid Embolism	semapv:ManualMappingCuration	2023-12-04
EFO:1001264	Anemia, Hemolytic, Autoimmune	skos:exactMatch	DOID:718	autoimmune hemolytic anemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001265	Aneurysm, False	skos:exactMatch	DOID:9005989	False Aneurysm	semapv:ManualMappingCuration	2023-12-04
EFO:1001266	Aniseikonia	skos:exactMatch	DOID:0050304	aniseikonia	semapv:ManualMappingCuration	2022-01-24
EFO:1001267	Aortic Coarctation	skos:exactMatch	DOID:9007908	Aortic Coarctation	semapv:ManualMappingCuration	2023-12-04
EFO:1001268	Aortic Rupture	skos:exactMatch	DOID:9004080	Aortic Rupture	semapv:ManualMappingCuration	2023-12-04
EFO:1001269	Arbovirus Infections	skos:exactMatch	DOID:9007579	Arbovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001269	Arbovirus Infections	skos:exactMatch	DOID:934	viral infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001270	Arterio-Arterial Fistula	skos:exactMatch	DOID:9003403	Arterio-Arterial Fistula	semapv:ManualMappingCuration	2023-12-04
EFO:1001271	Atrophic Vaginitis	skos:exactMatch	DOID:11968	postmenopausal atrophic vaginitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001272	bacterial pneumonia	skos:exactMatch	DOID:874	bacterial pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:1001274	Bone Anteversion	skos:exactMatch	DOID:9000114	Bone Anteversion	semapv:ManualMappingCuration	2023-12-04
EFO:1001275	Bordetella Infections	skos:exactMatch	DOID:9007021	Bordetella Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001276	Brain Stem Hemorrhage, Traumatic	skos:exactMatch	DOID:9000694	Brain Stem Hemorrhage, Traumatic	semapv:ManualMappingCuration	2023-12-04
EFO:1001277	Branchioma	skos:exactMatch	DOID:9005282	Branchioma	semapv:ManualMappingCuration	2023-12-04
EFO:1001278	Brown-Pearce carcinoma	skos:exactMatch	DOID:9006869	Brown-Pearce Carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001279	Brown-Sequard Syndrome	skos:exactMatch	DOID:606	Brown-Sequard syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001280	Burkholderia Infections	skos:exactMatch	DOID:9000739	Burkholderia Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001282	Candidemia	skos:exactMatch	DOID:9008452	Candidemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001283	Candidiasis, Invasive	skos:exactMatch	DOID:9000522	Invasive Candidiasis	semapv:ManualMappingCuration	2023-12-04
EFO:1001284	capillary leak syndrome	skos:exactMatch	DOID:14400	capillary leak syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001285	Cardiac Tamponade	skos:exactMatch	DOID:115	cardiac tamponade	semapv:ManualMappingCuration	2022-01-24
EFO:1001286	Caroli Disease	skos:exactMatch	DOID:0050876	Caroli disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001287	Cestode Infections	skos:exactMatch	DOID:9006970	Cestode Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001288	Chlamydiaceae Infections	skos:exactMatch	DOID:9008090	Chlamydiaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001289	Cholecystitis, Acute	skos:exactMatch	DOID:9007393	Acute Cholecystitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001290	chorea gravidarum	skos:exactMatch	DOID:14483	chorea gravidarum	semapv:ManualMappingCuration	2022-01-24
EFO:1001291	ciguatera poisoning	skos:exactMatch	DOID:9001470	Ciguatera Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:1001292	Circoviridae Infections	skos:exactMatch	DOID:9008580	Circoviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001293	collagenous colitis	skos:exactMatch	DOID:0060183	collagenous colitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001294	lymphocytic colitis	skos:exactMatch	DOID:0060184	lymphocytic colitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001295	microscopic colitis	skos:exactMatch	DOID:0060182	microscopic colitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001296	colon diverticulum	skos:exactMatch	DOID:9006657	Colon Diverticulum	semapv:ManualMappingCuration	2023-12-04
EFO:1001297	Coronary-Subclavian Steal Syndrome	skos:exactMatch	DOID:9002249	Coronary-Subclavian Steal Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001298	Coxa Vara	skos:exactMatch	DOID:9005226	Coxa Vara	semapv:ManualMappingCuration	2023-12-04
EFO:1001299	Crush Syndrome	skos:exactMatch	DOID:9000921	Crush Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001300	Cryptogenic Organizing Pneumonia	skos:exactMatch	DOID:0050157	cryptogenic organizing pneumonia	semapv:ManualMappingCuration	2022-01-24
EFO:1001301	Cubital Tunnel Syndrome	skos:exactMatch	DOID:9002629	Cubital Tunnel Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001302	Cytomegalovirus Retinitis	skos:exactMatch	DOID:0080160	cytomegalovirus retinitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001303	Deltaretrovirus Infections	skos:exactMatch	DOID:9001509	Deltaretrovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001304	Dental enamel hypoplasia	skos:exactMatch	DOID:693	dental enamel hypoplasia	semapv:ManualMappingCuration	2022-01-24
EFO:1001305	Dermatitis, Perioral	skos:exactMatch	DOID:9005617	Perioral Dermatitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001306	Diarrhea, Infantile	skos:exactMatch	DOID:9007847	Infantile Diarrhea	semapv:ManualMappingCuration	2023-12-04
EFO:1001307	dumping syndrome	skos:exactMatch	DOID:14495	dumping syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001308	Embolism, Paradoxical	skos:exactMatch	DOID:9005568	Paradoxical Embolism	semapv:ManualMappingCuration	2023-12-04
EFO:1001309	Encephalitis, Tick-Borne	skos:exactMatch	DOID:0050175	tick-borne encephalitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001310	Encephalitis, Varicella Zoster	skos:exactMatch	DOID:9002978	Varicella Zoster Encephalitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001311	End Stage Liver Disease	skos:exactMatch	DOID:9007996	End Stage Liver Disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001312	Endometritis	skos:exactMatch	DOID:1002	endometritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001313	Enterobacteriaceae Infections	skos:exactMatch	DOID:9003491	Enterobacteriaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001314	pseudomembranous enterocolitis	skos:exactMatch	DOID:0060185	Clostridium difficile colitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001315	Enzootic Bovine Leukosis	skos:exactMatch	DOID:9005637	Enzootic Bovine Leukosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001316	Eosinophilia-Myalgia Syndrome	skos:exactMatch	DOID:998	eosinophilia-myalgia syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001317	Epiphyses, Slipped	skos:exactMatch	DOID:9007203	Slipped Epiphyses	semapv:ManualMappingCuration	2023-12-04
EFO:1001318	Escherichia coli Infections	skos:exactMatch	DOID:9002953	Escherichia Coli Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001319	Euglenozoa Infections	skos:exactMatch	DOID:9007293	Euglenozoa Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001320	Exanthema Subitum	skos:exactMatch	DOID:0050495	exanthema subitum	semapv:ManualMappingCuration	2022-01-24
EFO:1001321	extrinsic allergic alveolitis	skos:exactMatch	DOID:841	extrinsic allergic alveolitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001322	eye foreign body	skos:exactMatch	DOID:9008361	Eye Foreign Bodies	semapv:ManualMappingCuration	2023-12-04
EFO:1001323	Eye Injuries, Penetrating	skos:exactMatch	DOID:9002560	Penetrating Eye Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:1001324	Fascioliasis	skos:exactMatch	DOID:885	fascioliasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001325	abdominal fibromatosis	skos:exactMatch	DOID:9006031	Abdominal Fibromatosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001326	Flavivirus Infections	skos:exactMatch	DOID:9004146	Flavivirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001327	Flavobacteriaceae Infections	skos:exactMatch	DOID:9002050	Flavobacteriaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001328	fluoride poisoning	skos:exactMatch	DOID:9000392	Fluoride Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:1001329	Follicular Cyst	skos:exactMatch	DOID:9006379	Follicular Cyst	semapv:ManualMappingCuration	2023-12-04
EFO:1001330	Foster-Kennedy syndrome	skos:exactMatch	DOID:14555	Foster-Kennedy syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001331	Genital neoplasm, female	skos:exactMatch	DOID:120	female reproductive organ cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1001331	Genital neoplasm, female	skos:exactMatch	DOID:9007399	Female Genital Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001332	Giant Lymph Node Hyperplasia	skos:exactMatch	DOID:0111157	Castleman disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001333	Glycogen Storage Disease Type 2b	skos:exactMatch	DOID:0050437	Danon disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001335	Gynatresia	skos:exactMatch	DOID:429	gynatresia	semapv:ManualMappingCuration	2022-01-24
EFO:1001336	Hammer Toe Syndrome	skos:exactMatch	DOID:9005398	Hammer Toe Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001337	Hand-Arm Vibration Syndrome	skos:exactMatch	DOID:9003649	Hand-Arm Vibration Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001339	Heart neoplasm	skos:exactMatch	DOID:9006547	Heart Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001340	Heat Stroke	skos:exactMatch	DOID:9004649	Heat Stroke	semapv:ManualMappingCuration	2023-12-04
EFO:1001341	Heavy Chain Disease	skos:exactMatch	DOID:0060125	heavy chain disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001342	Helminthiasis	skos:exactMatch	DOID:883	parasitic helminthiasis infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001343	Hemangioma, Cavernous, Central Nervous System	skos:exactMatch	DOID:0060669	cerebral cavernous malformation	semapv:ManualMappingCuration	2023-12-04
EFO:1001344	Hemarthrosis	skos:exactMatch	DOID:801	hemarthrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001345	Hepatitis, Alcoholic	skos:exactMatch	DOID:12351	alcoholic hepatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001346	Hepatopulmonary Syndrome	skos:exactMatch	DOID:900	hepatopulmonary syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001347	Herpes Labialis	skos:exactMatch	DOID:9004202	Herpes Labialis	semapv:ManualMappingCuration	2023-12-04
EFO:1001348	HIV-Associated Lipodystrophy Syndrome	skos:exactMatch	DOID:9008856	HIV-Associated Lipodystrophy Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001349	Human T-lymphotropic virus 2 infectious disease	skos:exactMatch	DOID:9003335	HTLV-II Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001350	Immunoblastic Lymphadenopathy	skos:exactMatch	DOID:9004253	Immunoblastic Lymphadenopathy	semapv:ManualMappingCuration	2023-12-04
EFO:1001351	infectious arthritis	skos:exactMatch	DOID:813	septic arthritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001352	Kartagener Syndrome	skos:exactMatch	DOID:0050144	Kartagener syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001353	Klebsiella Infections	skos:exactMatch	DOID:9003828	Klebsiella Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001354	Kleine-Levin Syndrome	skos:exactMatch	DOID:0060165	Kleine-Levin syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001355	Laryngopharyngeal Reflux	skos:exactMatch	DOID:9003366	Laryngopharyngeal Reflux	semapv:ManualMappingCuration	2023-12-04
EFO:1001356	Leiomyoma, Epithelioid	skos:exactMatch	DOID:9005549	Epithelioid Leiomyoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001357	Lentivirus Infections	skos:exactMatch	DOID:9005091	Lentivirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001358	Leprosy, Paucibacillary	skos:exactMatch	DOID:9001594	Paucibacillary Leprosy	semapv:ManualMappingCuration	2023-12-04
EFO:1001359	Leukocyte-Adhesion Deficiency Syndrome	skos:exactMatch	DOID:6612	leukocyte adhesion deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1001360	Leukoplakia, Hairy	skos:exactMatch	DOID:0060315	oral hairy leukoplakia	semapv:ManualMappingCuration	2023-12-04
EFO:1001361	localised scleroderma	skos:exactMatch	DOID:419	scleroderma	semapv:ManualMappingCuration	2022-01-24
EFO:1001361	localised scleroderma	skos:exactMatch	DOID:8472	localized scleroderma	semapv:ManualMappingCuration	2022-01-24
EFO:1001362	Lung Abscess	skos:exactMatch	DOID:0060317	lung abscess	semapv:ManualMappingCuration	2022-01-24
EFO:1001362	Lung Abscess	skos:exactMatch	DOID:850	lung disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001363	Lupus Vasculitis, Central Nervous System	skos:exactMatch	DOID:9005125	Lupus Vasculitis, Central Nervous System	semapv:ManualMappingCuration	2023-12-04
EFO:1001364	Lymphatic Metastasis	skos:exactMatch	DOID:9000081	Lymphatic Metastasis	semapv:ManualMappingCuration	2023-12-04
EFO:1001365	Lymphoma, AIDS-Related	skos:exactMatch	DOID:9000242	Lymphoma, AIDS-Related	semapv:ManualMappingCuration	2023-12-04
EFO:1001366	mastodynia	skos:exactMatch	DOID:9008722	Mastodynia	semapv:ManualMappingCuration	2023-12-04
EFO:1001367	Medial Tibial Stress Syndrome	skos:exactMatch	DOID:9007731	Medial Tibial Stress Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001368	Mediastinal Cyst	skos:exactMatch	DOID:9002759	Mediastinal Cysts	semapv:ManualMappingCuration	2023-12-04
EFO:1001369	Meningomyelocele	skos:exactMatch	DOID:0060326	myelomeningocele	semapv:ManualMappingCuration	2023-12-04
EFO:1001370	metatarsalgia	skos:exactMatch	DOID:9008541	Metatarsalgia	semapv:ManualMappingCuration	2023-12-04
EFO:1001371	Mixed Tumor, Mesodermal	skos:exactMatch	DOID:9001796	Mesodermal Mixed Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1001372	Monieziasis	skos:exactMatch	DOID:931	monieziasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001373	Multiple Organ Failure	skos:exactMatch	DOID:9002906	Multiple Organ Failure	semapv:ManualMappingCuration	2023-12-04
EFO:1001374	Mycoplasmatales Infections	skos:exactMatch	DOID:9008587	Mycoplasmatales Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001375	Myocardial Ischemia	skos:exactMatch	DOID:9007102	Myocardial Ischemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001376	Necrobiotic Xanthogranuloma	skos:exactMatch	DOID:9007969	Necrobiotic Xanthogranuloma	semapv:ManualMappingCuration	2023-12-04
EFO:1001377	Neisseriaceae Infections	skos:exactMatch	DOID:9008538	Neisseriaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001378	neurogenic arthropathy	skos:exactMatch	DOID:14286	neurogenic arthropathy	semapv:ManualMappingCuration	2022-01-24
EFO:1001379	neuroleptic malignant syndrome	skos:exactMatch	DOID:14464	neuroleptic malignant syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001380	Niemann-Pick disease	skos:exactMatch	DOID:14504	Niemann-Pick disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001381	Nocturnal Paroxysmal Dystonia	skos:exactMatch	DOID:9005450	Nocturnal Paroxysmal Dystonia	semapv:ManualMappingCuration	2023-12-04
EFO:1001382	Obesity Hypoventilation Syndrome	skos:exactMatch	DOID:9004753	Obesity Hypoventilation Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001383	Opsoclonus-Myoclonus Syndrome	skos:exactMatch	DOID:9001087	Opsoclonus-Myoclonus Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001384	Panniculitis, Peritoneal	skos:exactMatch	DOID:9006800	Peritoneal Panniculitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001385	Paralysis, Obstetric	skos:exactMatch	DOID:9008929	Obstetric Paralysis	semapv:ManualMappingCuration	2023-12-04
EFO:1001386	Pasteurellaceae Infections	skos:exactMatch	DOID:9008746	Pasteurellaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001387	Peliosis Hepatis	skos:exactMatch	DOID:914	peliosis hepatis	semapv:ManualMappingCuration	2022-01-24
EFO:1001388	Pelvic Inflammatory Disease	skos:exactMatch	DOID:1003	pelvic inflammatory disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001389	Peptic ulcer perforation	skos:exactMatch	DOID:752	peptic ulcer perforation	semapv:ManualMappingCuration	2022-01-24
EFO:1001390	Peri-Implantitis	skos:exactMatch	DOID:9003969	Peri-Implantitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001391	Periapical Periodontitis	skos:exactMatch	DOID:823	periapical periodontitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001392	Perimeningeal Infections	skos:exactMatch	DOID:9006960	Perimeningeal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001393	Periodontal Pocket	skos:exactMatch	DOID:9001352	Periodontal Pocket	semapv:ManualMappingCuration	2023-12-04
EFO:1001394	Peritoneal Fibrosis	skos:exactMatch	DOID:9002488	Peritoneal Fibrosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001395	Phlebitis	skos:exactMatch	DOID:864	phlebitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001396	Pinta	skos:exactMatch	DOID:1022	pinta disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001397	Piscirickettsiaceae Infections	skos:exactMatch	DOID:9006409	Piscirickettsiaceae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001398	Pneumocephalus	skos:exactMatch	DOID:9002018	Pneumocephalus	semapv:ManualMappingCuration	2023-12-04
EFO:1001399	Pneumonia, Aspiration	skos:exactMatch	DOID:3240	aspiration pneumonitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001400	Pneumopericardium	skos:exactMatch	DOID:9007273	Pneumopericardium	semapv:ManualMappingCuration	2023-12-04
EFO:1001401	Pneumovirus Infections	skos:exactMatch	DOID:9001953	Pneumovirus Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001402	postencephalitic Parkinson disease	skos:exactMatch	DOID:14332	postencephalitic Parkinson disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001403	postpartum thyroiditis	skos:exactMatch	DOID:9008005	Postpartum Thyroiditis	semapv:ManualMappingCuration	2023-12-04
EFO:1001404	Postpericardiotomy Syndrome	skos:exactMatch	DOID:9007295	Postpericardiotomy Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001406	Prosthesis-Related Infections	skos:exactMatch	DOID:9006516	Prosthesis-Related Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001407	Puerperal Infection	skos:exactMatch	DOID:9008718	Puerperal Infection	semapv:ManualMappingCuration	2023-12-04
EFO:1001408	Pulmonary Infarction	skos:exactMatch	DOID:8516	pulmonary embolism and infarction	semapv:ManualMappingCuration	2023-12-04
EFO:1001409	Pyomyositis	skos:exactMatch	DOID:876	pyomyositis	semapv:ManualMappingCuration	2022-01-24
EFO:1001410	Pythiosis	skos:exactMatch	DOID:9004704	Pythiosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001411	Radiation Pneumonitis	skos:exactMatch	DOID:9008604	Radiation Pneumonitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001412	renal colic	skos:exactMatch	DOID:9002274	Renal Colic	semapv:ManualMappingCuration	2023-12-04
EFO:1001413	Respiratory Syncytial Virus Infection	skos:exactMatch	DOID:1273	respiratory syncytial virus infectious disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001414	Retrobulbar Hemorrhage	skos:exactMatch	DOID:9008220	Retrobulbar Hemorrhage	semapv:ManualMappingCuration	2023-12-04
EFO:1001415	Retropharyngeal Abscess	skos:exactMatch	DOID:9006536	Retropharyngeal Abscess	semapv:ManualMappingCuration	2023-12-04
EFO:1001416	rheumatic fever nodule	skos:exactMatch	DOID:9007176	Rheumatic Nodule	semapv:ManualMappingCuration	2023-12-04
EFO:1001417	Rhinitis, Allergic, Perennial	skos:exactMatch	DOID:9003657	Perennial Allergic Rhinitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001418	Salmonella Infections	skos:exactMatch	DOID:0060859	salmonellosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001419	Schistosomiasis japonica	skos:exactMatch	DOID:0050597	intestinal schistosomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001419	Schistosomiasis japonica	skos:exactMatch	DOID:9002433	Schistosomiasis Japonica	semapv:ManualMappingCuration	2023-12-04
EFO:1001420	Schistosomiasis mansoni	skos:exactMatch	DOID:9002869	Schistosomiasis Mansoni	semapv:ManualMappingCuration	2023-12-04
EFO:1001421	Serratia Infections	skos:exactMatch	DOID:9004601	Serratia Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001422	Sertoli Cell-Only Syndrome	skos:exactMatch	DOID:0050457	Sertoli cell-only syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001423	Shaken Baby Syndrome	skos:exactMatch	DOID:9007358	Shaken Baby Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001424	skin epithelioid hemangioma	skos:exactMatch	DOID:14308	skin epithelioid hemangioma	semapv:ManualMappingCuration	2022-01-24
EFO:1001425	Skull Fractures	skos:exactMatch	DOID:9002209	Skull Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:1001426	Spinal Cord Ischemia	skos:exactMatch	DOID:9004922	Spinal Cord Ischemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001428	Subacute Combined Degeneration	skos:exactMatch	DOID:9007110	Subacute Combined Degeneration	semapv:ManualMappingCuration	2023-12-04
EFO:1001429	Subdural Effusion	skos:exactMatch	DOID:9001777	Subdural Effusion	semapv:ManualMappingCuration	2023-12-04
EFO:1001430	Sublingual Gland Neoplasms	skos:exactMatch	DOID:9008271	Sublingual Gland Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001431	suppurative thyroiditis	skos:exactMatch	DOID:14350	suppurative thyroiditis	semapv:ManualMappingCuration	2022-01-24
EFO:1001432	Tachycardia, Reciprocating	skos:exactMatch	DOID:9007178	Reciprocating Tachycardia	semapv:ManualMappingCuration	2023-12-04
EFO:1001433	Taeniasis	skos:exactMatch	DOID:0050596	taeniasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001434	Tendinopathy	skos:exactMatch	DOID:971	tendinitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001435	tenosynovitis	skos:exactMatch	DOID:970	tenosynovitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001436	thyroid nodule	skos:exactMatch	DOID:9005809	Thyroid Nodule	semapv:ManualMappingCuration	2023-12-04
EFO:1001437	Tracheal neoplasm	skos:relatedMatch	DOID:9003134	tracheal neoplasm	semapv:ManualMappingCuration	2023-12-04
EFO:1001438	Trematode Infections	skos:exactMatch	DOID:884	metagonimiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001438	Trematode Infections	skos:exactMatch	DOID:9004459	Trematode Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001439	Trilogy of Fallot	skos:exactMatch	DOID:9006477	Trilogy of Fallot	semapv:ManualMappingCuration	2023-12-04
EFO:1001440	Tuberculosis, Avian	skos:exactMatch	DOID:9000759	Avian Tuberculosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001441	Tuberculosis, Bovine	skos:exactMatch	DOID:9001011	Bovine Tuberculosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001442	cardiac tuberculosis	skos:exactMatch	DOID:0060570	cardiac tuberculosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001443	Tuberculosis, Cutaneous	skos:exactMatch	DOID:9005437	Cutaneous Tuberculosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001444	Tularemia	skos:exactMatch	DOID:2123	tularemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001445	Tungiasis	skos:exactMatch	DOID:0050266	tungiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001446	Uterine Inversion	skos:exactMatch	DOID:997	uterine inversion	semapv:ManualMappingCuration	2022-01-24
EFO:1001447	Vaginal neoplasm	skos:exactMatch	DOID:9006698	Vaginal Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001448	Ventricular Outflow Obstruction	skos:exactMatch	DOID:9004319	Ventricular Outflow Obstruction	semapv:ManualMappingCuration	2023-12-04
EFO:1001449	Vertebrobasilar insufficiency	skos:exactMatch	DOID:13003	vertebrobasilar insufficiency	semapv:ManualMappingCuration	2022-01-24
EFO:1001449	Vertebrobasilar insufficiency	skos:exactMatch	DOID:223	basilar artery insufficiency	semapv:ManualMappingCuration	2022-01-24
EFO:1001450	Wolff-Parkinson-White Syndrome	skos:exactMatch	DOID:384	Wolff-Parkinson-White syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001451	X-Linked Combined Immunodeficiency Diseases	skos:exactMatch	DOID:0060013	X-linked severe combined immunodeficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1001452	Yellow Nail Syndrome	skos:exactMatch	DOID:0050468	yellow nail syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001453	Zoster Sine Herpete	skos:exactMatch	DOID:9001709	Zoster Sine Herpete	semapv:ManualMappingCuration	2023-12-04
EFO:1001454	amnesia	skos:exactMatch	DOID:10914	amnestic disorder	semapv:ManualMappingCuration	2023-12-04
EFO:1001455	auditory system disease	skos:exactMatch	DOID:2742	auditory system disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001456	central nervous system infection	skos:exactMatch	DOID:9000025	Central Nervous System Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001458	diabetic cardiomyopathy	skos:exactMatch	DOID:9006945	Diabetic Cardiomyopathies	semapv:ManualMappingCuration	2023-12-04
EFO:1001459	diabetic foot	skos:exactMatch	DOID:9008212	Diabetic Foot	semapv:ManualMappingCuration	2023-12-04
EFO:1001462	erysipelas	skos:exactMatch	DOID:11330	erysipelas	semapv:ManualMappingCuration	2022-01-24
EFO:1001463	gastroenteritis	skos:exactMatch	DOID:2326	gastroenteritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001465	gliosarcoma	skos:exactMatch	DOID:3071	gliosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001467	Hypereosinophilic syndrome	skos:exactMatch	DOID:999	hypereosinophilic syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001469	Mantle cell lymphoma	skos:exactMatch	DOID:0050746	mantle cell lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001471	Merkel cell skin cancer	skos:exactMatch	DOID:3965	Merkel cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001472	Myelitis	skos:exactMatch	DOID:322	myelitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001473	Non-familial restrictive cardiomyopathy	skos:exactMatch	DOID:397	restrictive cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:1001474	pneumococcal pneumonia	skos:exactMatch	DOID:9002106	Pneumococcal Pneumonia	semapv:ManualMappingCuration	2023-12-04
EFO:1001475	schistosomiasis	skos:exactMatch	DOID:1395	schistosomiasis	semapv:ManualMappingCuration	2022-01-24
EFO:1001477	Systemic capillary leak syndrome	skos:exactMatch	DOID:14400	capillary leak syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001478	systemic inflammatory response syndrome	skos:exactMatch	DOID:9000169	Systemic Inflammatory Response Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001479	Tumor Lysis Syndrome	skos:exactMatch	DOID:9003827	Tumor Lysis Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001481	enterocolitis	skos:exactMatch	DOID:9002805	Enterocolitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001482	cardiotoxicity	skos:exactMatch	DOID:9002371	Cardiotoxicity	semapv:ManualMappingCuration	2023-12-04
EFO:1001483	non-obstructive coronary artery disease	skos:exactMatch	DOID:0080938	nonobstructive coronary artery disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001484	pain agnosia	skos:exactMatch	DOID:0060145	pain agnosia	semapv:ManualMappingCuration	2022-01-24
EFO:1001485	acromegaly	skos:exactMatch	DOID:2449	acromegaly	semapv:ManualMappingCuration	2022-01-24
EFO:1001486	primary biliary cirrhosis	skos:exactMatch	DOID:12236	primary biliary cholangitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001487	secondary biliary cirrhosis	skos:exactMatch	DOID:12236	primary biliary cholangitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001489	skin and soft tissue Staphylococcus aureus infection	skos:exactMatch	DOID:9008885	Staphylococcal Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001490	late-onset myasthenia gravis	skos:exactMatch	DOID:437	myasthenia gravis	semapv:ManualMappingCuration	2023-12-04
EFO:1001491	abortion	skos:exactMatch	DOID:9003281	Spontaneous Abortions	semapv:ManualMappingCuration	2023-12-04
EFO:1001492	atrophic macular degeneration	skos:exactMatch	DOID:9001427	Geographic Atrophy	semapv:ManualMappingCuration	2023-12-04
EFO:1001495	small artery occlusion	skos:exactMatch	DOID:9007434	small artery occlusion	semapv:ManualMappingCuration	2023-12-04
EFO:1001496	Autosomal dominant polycystic kidney disease	skos:exactMatch	DOID:898	autosomal dominant polycystic kidney disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001497	cardiac conduction defect	skos:exactMatch	DOID:9001836	Cardiac Conduction Defect	semapv:ManualMappingCuration	2023-12-04
EFO:1001498	disseminated atypical mycobacterial infection	skos:exactMatch	DOID:9004729	Nontuberculous Mycobacterium Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001499	histiocytic medullary reticulosis	skos:exactMatch	DOID:0080915	histiocytic sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001500	intellectual disability with language impairment	skos:exactMatch	DOID:0111331	intellectual disability-severe speech delay-mild dysmorphism syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001501	pulmonary fibrosis and/or bone marrow failure, telomere-related, 1	skos:exactMatch	DOID:9005221	Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome, Telomere-Related, 1	semapv:ManualMappingCuration	2023-12-04
EFO:1001502	rasopathy	skos:exactMatch	DOID:0080690	RASopathy	semapv:ManualMappingCuration	2023-03-17
EFO:1001503	type II diabetes mellitus with acanthosis nigricans	skos:exactMatch	DOID:9001751	Insulin-Resistant Diabetes Mellitus, with Acanthosis Nigricans	semapv:ManualMappingCuration	2023-12-04
EFO:1001504	small vessel stroke	skos:exactMatch	DOID:9007096	Stroke	semapv:ManualMappingCuration	2023-12-04
EFO:1001505	cystic liver disease	skos:exactMatch	DOID:0050770	polycystic liver disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001506	primary angle closure glaucoma	skos:exactMatch	DOID:1405	primary angle-closure glaucoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001507	asparaginase-induced acute pancreatitis	skos:exactMatch	DOID:2913	acute pancreatitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001510	specific language impairment	skos:exactMatch	DOID:0060244	specific language impairment	semapv:ManualMappingCuration	2022-01-24
EFO:1001511	monogenic diabetes	skos:exactMatch	DOID:9351	diabetes mellitus	semapv:ManualMappingCuration	2023-12-04
EFO:1001512	endometrial carcinoma	skos:exactMatch	DOID:2871	endometrial carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001513	liver neoplasm	skos:exactMatch	DOID:9007188	Liver Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001513	liver neoplasm	skos:exactMatch	DOID:916	liver benign neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001514	endometrial endometrioid carcinoma	skos:exactMatch	DOID:2870	endometrial adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001515	ovarian endometrioid carcinoma	skos:exactMatch	DOID:5828	endometrioid ovary carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001516	ovarian serous carcinoma	skos:exactMatch	DOID:0050933	ovarian serous carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001517	renal fibrosis	skos:exactMatch	DOID:0050855	renal fibrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001518	heavy metal poisoning	skos:exactMatch	DOID:9000659	Heavy Metal Toxicity	semapv:ManualMappingCuration	2023-12-04
EFO:1001753	abdominal abscess	skos:exactMatch	DOID:9008115	Abdominal Abscess	semapv:ManualMappingCuration	2023-12-04
EFO:1001754	Abruptio Placentae	skos:exactMatch	DOID:9667	placental abruption	semapv:ManualMappingCuration	2022-01-24
EFO:1001755	accelerated phase myeloid leukemia	skos:exactMatch	DOID:9001865	Myeloid Leukemia, Accelerated Phase	semapv:ManualMappingCuration	2023-12-04
EFO:1001756	Acrodynia	skos:exactMatch	DOID:9004742	Acrodynia	semapv:ManualMappingCuration	2023-12-04
EFO:1001757	Adenomyosis	skos:exactMatch	DOID:288	endometriosis of uterus	semapv:ManualMappingCuration	2023-12-04
EFO:1001758	ageusia	skos:exactMatch	DOID:9006039	Ageusia	semapv:ManualMappingCuration	2023-12-04
EFO:1001759	alcohol amnestic disorder	skos:exactMatch	DOID:9008602	Alcohol Amnestic Disorder	semapv:ManualMappingCuration	2023-12-04
EFO:1001760	aneurysmal bone cyst	skos:exactMatch	DOID:9005719	Aneurysmal Bone Cysts	semapv:ManualMappingCuration	2023-12-04
EFO:1001761	Angiofibroma	skos:exactMatch	DOID:9000915	Angiofibroma	semapv:ManualMappingCuration	2023-12-04
EFO:1001762	autonomic dysreflexia	skos:exactMatch	DOID:9001461	Autonomic Dysreflexia	semapv:ManualMappingCuration	2023-12-04
EFO:1001763	basal cell neoplasm	skos:exactMatch	DOID:9003929	Basal Cell Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001764	Birnaviridae Infections	skos:exactMatch	DOID:9006589	Birnaviridae Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001765	Bovine mastitis	skos:exactMatch	DOID:9008258	Bovine Mastitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001766	brain hypoxia	skos:exactMatch	DOID:9004756	Brain Hypoxia	semapv:ManualMappingCuration	2023-12-04
EFO:1001767	brain stem neoplasm	skos:exactMatch	DOID:9002777	Brain Stem Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001768	cadmium poisoning	skos:exactMatch	DOID:9001191	Cadmium Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:1001769	carcinoid heart disease	skos:exactMatch	DOID:9005906	Carcinoid Heart Disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001770	Carcinoma, Lewis Lung	skos:exactMatch	DOID:9003690	Carcinoma, Lewis Lung	semapv:ManualMappingCuration	2023-12-04
EFO:1001771	cardiac edema	skos:exactMatch	DOID:9002860	Cardiac Edema	semapv:ManualMappingCuration	2023-12-04
EFO:1001772	Central Cord Syndrome	skos:exactMatch	DOID:9001711	Central Cord Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001773	Central Nervous System Helminthiasis	skos:exactMatch	DOID:9000928	Central Nervous System Helminthiasis	semapv:ManualMappingCuration	2023-12-04
EFO:1001774	central nervous system venous angioma	skos:exactMatch	DOID:9006290	Central Nervous System Venous Angioma	semapv:ManualMappingCuration	2023-12-04
EFO:1001775	cerebrospinal fluid otorrhea	skos:exactMatch	DOID:9004660	Cerebrospinal Fluid Otorrhea	semapv:ManualMappingCuration	2023-12-04
EFO:1001776	Chilaiditi Syndrome	skos:exactMatch	DOID:9006499	Chilaiditi Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001777	chloracne	skos:exactMatch	DOID:9001341	Chloracne	semapv:ManualMappingCuration	2023-12-04
EFO:1001778	chromosome-defective micronuclei	skos:exactMatch	DOID:9006676	Micronuclei, Chromosome-Defective	semapv:ManualMappingCuration	2023-12-04
EFO:1001779	chronic myelomonocytic leukemia	skos:exactMatch	DOID:0080188	chronic myelomonocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001780	Chylothorax	skos:exactMatch	DOID:9007840	Chylothorax	semapv:ManualMappingCuration	2023-12-04
EFO:1001781	Commotio Cordis	skos:exactMatch	DOID:9001823	Commotio Cordis	semapv:ManualMappingCuration	2023-12-04
EFO:1001782	dental pulp exposure	skos:exactMatch	DOID:9000930	Dental Pulp Exposure	semapv:ManualMappingCuration	2023-12-04
EFO:1001783	desmoplastic fibroma	skos:exactMatch	DOID:9004141	Desmoplastic Fibroma	semapv:ManualMappingCuration	2023-12-04
EFO:1001784	diffuse cutaneous Leishmaniasis	skos:exactMatch	DOID:9003868	Diffuse Cutaneous Leishmaniasis	semapv:ManualMappingCuration	2023-12-04
EFO:1001785	diffuse esophageal spasm	skos:exactMatch	DOID:9007276	Diffuse Esophageal Spasm	semapv:ManualMappingCuration	2023-12-04
EFO:1001786	erythroplasia	skos:exactMatch	DOID:9007394	Erythroplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1001787	experimental arthritis	skos:exactMatch	DOID:9002457	Experimental Arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:1001788	Eye Burns	skos:exactMatch	DOID:9000173	Eye Burns	semapv:ManualMappingCuration	2023-12-04
EFO:1001789	familial apolipoprotein B hypobetalipoproteinemia	skos:exactMatch	DOID:9002123	Familial Hypobetalipoproteinemia, Apolipoprotein B	semapv:ManualMappingCuration	2023-12-04
EFO:1001790	female athlete triad syndrome	skos:exactMatch	DOID:9008759	Female Athlete Triad Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001791	femoral hernia	skos:exactMatch	DOID:9004455	Femoral Hernia	semapv:ManualMappingCuration	2023-12-04
EFO:1001792	femoral neck fracture	skos:exactMatch	DOID:9001417	Femoral Neck Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:1001793	fetal hypoxia	skos:exactMatch	DOID:9007877	Fetal Hypoxia	semapv:ManualMappingCuration	2023-12-04
EFO:1001794	fetomaternal transfusion	skos:exactMatch	DOID:9007354	Fetomaternal Transfusion	semapv:ManualMappingCuration	2023-12-04
EFO:1001795	fusariosis	skos:exactMatch	DOID:0050289	fusariosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001796	Glomus Jugulare Tumor	skos:exactMatch	DOID:9002449	Glomus Jugulare Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1001797	Hemoglobin SC Disease	skos:exactMatch	DOID:9006672	Hemoglobin SC Disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001798	immunoproliferative small intestinal disease	skos:exactMatch	DOID:0060126	alpha chain disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001799	incomplete abortion	skos:exactMatch	DOID:9007547	Incomplete Abortion	semapv:ManualMappingCuration	2023-12-04
EFO:1001800	Intervertebral Disc Displacement	skos:exactMatch	DOID:9006086	Intervertebral Disc Displacement	semapv:ManualMappingCuration	2023-12-04
EFO:1001801	intracranial subdural hematoma	skos:exactMatch	DOID:9003292	Intracranial Subdural Hematoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001802	isolated noncompaction of the ventricular myocardium	skos:exactMatch	DOID:9000596	Isolated Noncompaction of the Ventricular Myocardium	semapv:ManualMappingCuration	2023-12-04
EFO:1001803	lingual thyroid	skos:exactMatch	DOID:9000704	Lingual Thyroids	semapv:ManualMappingCuration	2023-12-04
EFO:1001804	Livedo reticularis	skos:exactMatch	DOID:9001467	Livedo Reticularis	semapv:ManualMappingCuration	2023-12-04
EFO:1001805	lobomycosis	skos:exactMatch	DOID:13026	lobomycosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001806	macrophage activation syndrome	skos:exactMatch	DOID:9002798	Macrophage Activation Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001807	malacoplakia	skos:exactMatch	DOID:9004625	Malacoplakia	semapv:ManualMappingCuration	2023-12-04
EFO:1001808	manganese poisoning	skos:exactMatch	DOID:9000304	Manganese Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:1001809	Marchiafava-Bignami Disease	skos:exactMatch	DOID:9003718	Marchiafava-Bignami Disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001810	mercury poisoning	skos:exactMatch	DOID:9003709	Mercury Poisoning	semapv:ManualMappingCuration	2023-12-04
EFO:1001811	Monteggia's fracture	skos:exactMatch	DOID:9004580	Monteggia's Fracture	semapv:ManualMappingCuration	2023-12-04
EFO:1001812	myringosclerosis	skos:exactMatch	DOID:1214	tympanosclerosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001813	Nasal Septal Perforation	skos:exactMatch	DOID:9005431	Nasal Septal Perforation	semapv:ManualMappingCuration	2023-12-04
EFO:1001814	nephrogenic fibrosing dermopathy	skos:exactMatch	DOID:9007889	Nephrogenic Fibrosing Dermopathy	semapv:ManualMappingCuration	2023-12-04
EFO:1001815	nervous system heavy metal poisoning	skos:exactMatch	DOID:9001363	Heavy Metal Poisoning, Nervous System	semapv:ManualMappingCuration	2023-12-04
EFO:1001816	neutropenic enterocolitis	skos:exactMatch	DOID:9002503	Neutropenic Enterocolitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001817	ocular posterior capsular rupture	skos:exactMatch	DOID:9008947	Posterior Capsular Rupture, Ocular	semapv:ManualMappingCuration	2023-12-04
EFO:1001818	oral submucous fibrosis	skos:exactMatch	DOID:5773	oral submucous fibrosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001819	orbital myositis	skos:exactMatch	DOID:9002988	Orbital Myositis	semapv:ManualMappingCuration	2023-12-04
EFO:1001820	oroficial granulomatosis	skos:exactMatch	DOID:9000125	Orofacial Granulomatosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001821	osteoradionecrosis	skos:exactMatch	DOID:9008321	Osteoradionecrosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001822	Paroxysmal Hemicrania	skos:exactMatch	DOID:9002176	Paroxysmal Hemicrania	semapv:ManualMappingCuration	2023-12-04
EFO:1001823	Periprosthetic Fractures	skos:exactMatch	DOID:9003427	Periprosthetic Fractures	semapv:ManualMappingCuration	2023-12-04
EFO:1001824	pinguecula	skos:exactMatch	DOID:11029	pinguecula	semapv:ManualMappingCuration	2022-01-24
EFO:1001825	pleurisy	skos:exactMatch	DOID:10247	pleurisy	semapv:ManualMappingCuration	2022-01-24
EFO:1001826	Poroma	skos:exactMatch	DOID:9003527	Poroma	semapv:ManualMappingCuration	2023-12-04
EFO:1001827	post-concussion syndrome	skos:exactMatch	DOID:9008219	Post-Concussion Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001828	post-exercise hypotension	skos:exactMatch	DOID:9004717	Post-Exercise Hypotension	semapv:ManualMappingCuration	2023-12-04
EFO:1001829	Posterior Leukoencephalopathy Syndrome	skos:exactMatch	DOID:9001074	Posterior Leukoencephalopathy Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001830	precursor T-cell lymphoblastic leukemia-lymphoma	skos:exactMatch	DOID:5603	T-cell acute lymphoblastic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001831	pseudolymphoma	skos:exactMatch	DOID:9005797	Pseudolymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001832	Psoas abscess	skos:exactMatch	DOID:9002880	Psoas Abscess	semapv:ManualMappingCuration	2023-12-04
EFO:1001833	Pubic Symphysis Diastasis	skos:exactMatch	DOID:9001687	Pubic Symphysis Diastasis	semapv:ManualMappingCuration	2023-12-04
EFO:1001834	pulmonary aspergillosis	skos:exactMatch	DOID:0050153	pulmonary aspergilloma	semapv:ManualMappingCuration	2022-01-24
EFO:1001835	pyelocystitis	skos:exactMatch	DOID:9007999	Pyelocystitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001836	pyogenic liver abscess	skos:exactMatch	DOID:9004142	Pyogenic Liver Abscesses	semapv:ManualMappingCuration	2023-12-04
EFO:1001837	rectocele	skos:exactMatch	DOID:9008151	Rectocele	semapv:ManualMappingCuration	2023-12-04
EFO:1001838	renal nutcracker syndrome	skos:exactMatch	DOID:9007228	Renal Nutcracker Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001839	respiratory aspiration	skos:exactMatch	DOID:9001264	Respiratory Aspiration	semapv:ManualMappingCuration	2023-12-04
EFO:1001840	respiratory paralysis	skos:exactMatch	DOID:9000292	Respiratory Paralysis	semapv:ManualMappingCuration	2023-12-04
EFO:1001841	sebaceous of Jadassohn nevus	skos:exactMatch	DOID:0111530	linear nevus sebaceous syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001842	Serotonin Syndrome	skos:exactMatch	DOID:9002607	Serotonin Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001843	sinoatrial nodal reentry tachycardia	skos:exactMatch	DOID:9004944	Tachycardia, Sinoatrial Nodal Reentry	semapv:ManualMappingCuration	2023-12-04
EFO:1001844	skin mastocytoma	skos:exactMatch	DOID:3666	solitary mastocytoma of the skin	semapv:ManualMappingCuration	2022-01-24
EFO:1001845	spinal cord compression	skos:exactMatch	DOID:9001553	Spinal Cord Compression	semapv:ManualMappingCuration	2023-12-04
EFO:1001846	Spinal Osteophytosis	skos:exactMatch	DOID:9003439	Spinal Osteophytosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001847	spinal subdural hematoma	skos:exactMatch	DOID:9005866	Spinal Subdural Hematoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001848	squamous odontogenic tumor	skos:exactMatch	DOID:9004613	Squamous Odontogenic Tumor	semapv:ManualMappingCuration	2023-12-04
EFO:1001849	staphylococcal skin infections	skos:exactMatch	DOID:9005966	Staphylococcal Skin Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001850	stomach diverticulum	skos:exactMatch	DOID:9007206	Stomach Diverticulum	semapv:ManualMappingCuration	2023-12-04
EFO:1001851	stomach rupture	skos:exactMatch	DOID:9004275	Stomach Rupture	semapv:ManualMappingCuration	2023-12-04
EFO:1001852	Stomach Volvulus	skos:exactMatch	DOID:9005142	Stomach Volvulus	semapv:ManualMappingCuration	2023-12-04
EFO:1001853	submandibular gland neoplasm	skos:exactMatch	DOID:9008501	Submandibular Gland Neoplasms	semapv:ManualMappingCuration	2023-12-04
EFO:1001854	subphrenic abscess	skos:exactMatch	DOID:9007378	Subphrenic Abscess	semapv:ManualMappingCuration	2023-12-04
EFO:1001855	Superior Vena Cava Syndrome	skos:exactMatch	DOID:9000139	Superior Vena Cava Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001856	Susac Syndrome	skos:exactMatch	DOID:9004457	Susac Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001857	Takayasu arteritis	skos:exactMatch	DOID:2508	Takayasu's arteritis	semapv:ManualMappingCuration	2022-01-24
EFO:1001858	Tarlov Cysts	skos:exactMatch	DOID:9000482	Tarlov Cysts	semapv:ManualMappingCuration	2023-12-04
EFO:1001859	testicular hydrocele	skos:exactMatch	DOID:9912	hydrocele	semapv:ManualMappingCuration	2023-12-04
EFO:1001860	thymus hyperplasia	skos:exactMatch	DOID:9004911	Thymus Hyperplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1001861	traumatic diaphragmatic hernia	skos:exactMatch	DOID:9001421	Diaphragmatic Hernia, Traumatic	semapv:ManualMappingCuration	2023-12-04
EFO:1001862	urinary bladder fistula	skos:exactMatch	DOID:9006172	Urinary Bladder Fistula	semapv:ManualMappingCuration	2023-12-04
EFO:1001863	Uterine Inertia	skos:exactMatch	DOID:9001832	Uterine Inertia	semapv:ManualMappingCuration	2023-12-04
EFO:1001864	uterine prolapse	skos:exactMatch	DOID:9004984	Uterine Prolapse	semapv:ManualMappingCuration	2023-12-04
EFO:1001865	ventilator-associated pneumonia	skos:exactMatch	DOID:9004257	Pneumonia, Ventilator-Associated	semapv:ManualMappingCuration	2023-12-04
EFO:1001867	Zenker diverticulum	skos:exactMatch	DOID:9004620	Zenker Diverticulum	semapv:ManualMappingCuration	2023-12-04
EFO:1001868	congenital contractures of the limbs and face, hypotonia, and developmental delay	skos:exactMatch	DOID:0081048	congenital limbs-face contractures-hypotonia-developmental delay syndrome	semapv:ManualMappingCuration	2023-04-17
EFO:1001869	dysentery	skos:exactMatch	DOID:12384	dysentery	semapv:ManualMappingCuration	2022-01-24
EFO:1001870	late-onset Alzheimers disease	skos:exactMatch	DOID:10652	Alzheimer's disease	semapv:ManualMappingCuration	2023-12-04
EFO:1001871	acquired cold urticaria	skos:exactMatch	DOID:0060220	physical urticaria	semapv:ManualMappingCuration	2023-12-04
EFO:1001872	agoraphobia	skos:exactMatch	DOID:593	agoraphobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001873	AIDS phobia	skos:exactMatch	DOID:603	AIDS phobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001874	amyloidoma	skos:exactMatch	DOID:9007454	amyloidoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001875	amyloidosis	skos:exactMatch	DOID:9120	amyloidosis	semapv:ManualMappingCuration	2022-01-24
EFO:1001876	animal phobia	skos:exactMatch	DOID:600	animal phobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001878	blood-injection-injury phobia	skos:exactMatch	DOID:599	specific phobia	semapv:ManualMappingCuration	2023-12-04
EFO:1001879	cancerophobia	skos:exactMatch	DOID:602	cancerophobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001880	chemotherapy-induced gastrointestinal mucositis	skos:exactMatch	DOID:0080178	mucositis	semapv:ManualMappingCuration	2023-12-04
EFO:1001881	cold urticaria	skos:exactMatch	DOID:0060220	physical urticaria	semapv:ManualMappingCuration	2023-12-04
EFO:1001882	cutaneous nodular amyloidosis	skos:exactMatch	DOID:9001902	cutaneous nodular amyloidosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001883	Dendritic keratitis	skos:exactMatch	DOID:9008162	Dendritic Keratitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001884	dental phobia	skos:exactMatch	DOID:9003606	dental phobia	semapv:ManualMappingCuration	2023-12-04
EFO:1001887	epicondylitis	skos:exactMatch	DOID:14087	epicondylitis	semapv:ManualMappingCuration	2022-01-24
EFO:1001888	eye infection	skos:exactMatch	DOID:9008201	Eye Infections	semapv:ManualMappingCuration	2023-12-04
EFO:1001889	flying phobia	skos:exactMatch	DOID:605	flying phobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001890	food allergy	skos:exactMatch	DOID:3044	food allergy	semapv:ManualMappingCuration	2022-01-24
EFO:1001892	generalized anxiety disorder	skos:exactMatch	DOID:14320	generalized anxiety disorder	semapv:ManualMappingCuration	2022-01-24
EFO:1001893	Hand-foot syndrome	skos:exactMatch	DOID:9005708	Hand-Foot Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001896	lateral epicondylitis	skos:exactMatch	DOID:14087	epicondylitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001898	mucositis	skos:exactMatch	DOID:0080178	mucositis	semapv:ManualMappingCuration	2023-12-04
EFO:1001900	myoclonic epilepsy	skos:exactMatch	DOID:9005154	Myoclonic Epilepsies	semapv:ManualMappingCuration	2023-12-04
EFO:1001901	neuroendocrine neoplasm	skos:exactMatch	DOID:169	neuroendocrine tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1001902	neuromuscular disease	skos:exactMatch	DOID:440	neuromuscular disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001903	nosophobia	skos:exactMatch	DOID:0060048	nosophobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001904	oral mucositis	skos:exactMatch	DOID:9637	stomatitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001907	panic disorder without agoraphobia	skos:exactMatch	DOID:594	panic disorder	semapv:ManualMappingCuration	2023-12-04
EFO:1001908	phobic disorder	skos:exactMatch	DOID:591	phobic disorder	semapv:ManualMappingCuration	2022-01-24
EFO:1001909	Plantar Fasciitis	skos:exactMatch	DOID:9600	plantar fasciitis	semapv:ManualMappingCuration	2023-12-04
EFO:1001910	pulmonary amyloidosis	skos:exactMatch	DOID:9003080	pulmonary amyloidosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001911	pulmonary nodular amyloidosis	skos:exactMatch	DOID:9003080	pulmonary amyloidosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001913	Purpura Fulminans	skos:exactMatch	DOID:0060538	purpura fulminans	semapv:ManualMappingCuration	2023-12-04
EFO:1001916	separation anxiety disorder	skos:exactMatch	DOID:10685	separation anxiety disorder	semapv:ManualMappingCuration	2022-01-24
EFO:1001917	social anxiety disorder	skos:exactMatch	DOID:11257	social phobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001918	specific phobia	skos:exactMatch	DOID:599	specific phobia	semapv:ManualMappingCuration	2022-01-24
EFO:1001919	Spinal cord injury	skos:exactMatch	DOID:9000039	Spinal Cord Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:1001923	varicose ulcer	skos:exactMatch	DOID:9004272	Varicose Ulcer	semapv:ManualMappingCuration	2023-12-04
EFO:1001925	pneumococcal bacteremia	skos:exactMatch	DOID:9001298	pneumococcal bacteremia	semapv:ManualMappingCuration	2023-12-04
EFO:1001926	pathological gambling	skos:exactMatch	DOID:12399	pathological gambling	semapv:ManualMappingCuration	2022-01-24
EFO:1001927	cutaneous squamous cell carcinoma	skos:exactMatch	DOID:3151	skin squamous cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001928	small intestine neuroendocrine tumor	skos:exactMatch	DOID:4434	small intestine neuroendocrine neoplasm	semapv:ManualMappingCuration	2022-01-24
EFO:1001929	selective IgA deficiency disease	skos:exactMatch	DOID:0060025	immunoglobulin alpha deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:1001929	selective IgA deficiency disease	skos:exactMatch	DOID:11701	selective IgA deficiency disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001930	idiopathic osteonecrosis of the femoral head	skos:exactMatch	DOID:9003049	Femur Head Necrosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001931	oropharynx cancer	skos:exactMatch	DOID:8557	oropharynx cancer	semapv:ManualMappingCuration	2022-01-24
EFO:1001932	adult acute megakaryoblastic leukemia	skos:exactMatch	DOID:8761	acute megakaryocytic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001933	adult acute monocytic leukemia	skos:exactMatch	DOID:0080149	adult acute monocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001934	adult acute myeloid leukemia	skos:exactMatch	DOID:9119	acute myeloid leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001935	adult B acute lymphoblastic leukemia	skos:exactMatch	DOID:0060592	B-cell adult acute lymphocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001936	adult T acute lymphoblastic leukemia	skos:exactMatch	DOID:5602	T-cell adult acute lymphocytic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001937	amelanotic melanoma	skos:exactMatch	DOID:4359	amelanotic melanoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001938	B-cell non-Hodgkins lymphoma	skos:exactMatch	DOID:707	B-cell lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001939	Barrett adenocarcinoma	skos:exactMatch	DOID:7941	Barrett's adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001940	basaloid squamous cell carcinoma	skos:exactMatch	DOID:5522	basaloid squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001941	bronchioloalveolar carcinoma	skos:exactMatch	DOID:4926	bronchiolo-alveolar adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001942	bronchogenic carcinoma	skos:exactMatch	DOID:3904	bronchus carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001943	childhood acute megakaryoblastic leukemia	skos:exactMatch	DOID:0080794	childhood acute megakaryoblastic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001944	childhood acute monocytic leukemia	skos:exactMatch	DOID:8864	acute monocytic leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001945	childhood acute myeloid leukemia with maturation	skos:exactMatch	DOID:0070323	childhood acute myeloid leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001946	childhood B acute lymphoblastic leukemia	skos:exactMatch	DOID:0080146	childhood B-cell acute lymphoblastic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001947	childhood T acute lymphoblastic leukemia	skos:exactMatch	DOID:0080145	childhood T-cell acute lymphoblastic leukemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001948	childhood T lymphoblastic lymphoma	skos:exactMatch	DOID:0080148	T-cell childhood lymphoblastic lymphoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001949	colon adenocarcinoma	skos:exactMatch	DOID:234	colon adenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001950	colon carcinoma	skos:exactMatch	DOID:1520	colon carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001951	colorectal carcinoma	skos:exactMatch	DOID:0080199	colorectal carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001951	colorectal carcinoma	skos:exactMatch	DOID:0080200	bilateral renal aplasia	semapv:ManualMappingCuration	2023-12-04
EFO:1001952	endometrial adenosquamous carcinoma	skos:exactMatch	DOID:5631	endometrial adenosquamous carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001953	endometrial endometrioid adenocarcinoma, variant with squamous differentiation	skos:exactMatch	DOID:2870	endometrial adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001954	Epstein-Barr virus-related Burkitts lymphoma	skos:exactMatch	DOID:8584	Burkitt lymphoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001955	erythroleukemia	skos:exactMatch	DOID:0080916	erythroleukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1001956	gallbladder carcinoma	skos:exactMatch	DOID:4948	gallbladder carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001957	hereditary thyroid gland medullary carcinoma	skos:exactMatch	DOID:0050547	familial medullary thyroid carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001958	high grade ovarian serous adenocarcinoma	skos:exactMatch	DOID:5744	ovary serous adenocarcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001959	hilar cholangiocarcinoma	skos:exactMatch	DOID:4927	Klatskin's tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1001960	hypopharyngeal squamous cell carcinoma	skos:exactMatch	DOID:9005472	hypopharyngeal squamous cell carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001961	intrahepatic cholangiocarcinoma	skos:exactMatch	DOID:4928	intrahepatic cholangiocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001962	ovarian cystadenocarcinoma	skos:exactMatch	DOID:3605	ovarian cystadenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001963	ovarian mucinous cystadenocarcinoma	skos:exactMatch	DOID:3604	ovarian mucinous cystadenocarcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001964	pancreatic somatostatinoma	skos:exactMatch	DOID:4432	pancreatic somatostatinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001965	pharyngeal squamous cell carcinoma	skos:exactMatch	DOID:0050921	pharynx squamous cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001966	rectosigmoid adenocarcinoma	skos:exactMatch	DOID:2781	rectosigmoid cancer	semapv:ManualMappingCuration	2023-12-04
EFO:1001967	salivary gland squamous cell carcinoma	skos:exactMatch	DOID:0050904	salivary gland carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001968	soft tissue sarcoma	skos:exactMatch	DOID:1115	sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001969	squamous cell breast carcinoma, acantholytic variant	skos:exactMatch	DOID:7459	acantholytic variant squamous cell breast carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001970	squamous papilloma	skos:exactMatch	DOID:139	squamous cell papilloma	semapv:ManualMappingCuration	2022-01-24
EFO:1001971	thyroid gland sarcoma	skos:exactMatch	DOID:4515	thyroid sarcoma	semapv:ManualMappingCuration	2023-12-04
EFO:1001972	undifferentiated pleomorphic sarcoma	skos:exactMatch	DOID:1907	malignant fibrous histiocytoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001973	ureter urothelial carcinoma	skos:exactMatch	DOID:6888	ureter transitional cell carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001974	uterine leiomyosarcoma	skos:exactMatch	DOID:5289	uterus leiomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001975	vulvar leiomyosarcoma	skos:exactMatch	DOID:5286	vulvar leiomyosarcoma	semapv:ManualMappingCuration	2022-01-24
EFO:1001976	cardioembolic stroke	skos:exactMatch	DOID:9000243	cardioembolic stroke	semapv:ManualMappingCuration	2023-12-04
EFO:1001977	3MC syndrome 2	skos:exactMatch	DOID:0060576	3MC syndrome 2	semapv:ManualMappingCuration	2022-01-24
EFO:1001978	3MC syndrome 1	skos:exactMatch	DOID:0060575	3MC syndrome 1	semapv:ManualMappingCuration	2022-01-24
EFO:1001979	Adrenocorticotropic hormone deficiency	skos:exactMatch	DOID:0080150	adrenocorticotropic hormone deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:1001980	Alpha-methylacyl-CoA racemase deficiency	skos:exactMatch	DOID:0060602	alpha-methylacyl-CoA racemase deficiency	semapv:ManualMappingCuration	2022-01-24
EFO:1001981	Aminoacylase 1 deficiency	skos:exactMatch	DOID:9003016	Aminoacylase 1 Deficiency	semapv:ManualMappingCuration	2023-12-04
EFO:1001982	Antisynthetase syndrome	skos:exactMatch	DOID:0080744	antisynthetase syndrome	semapv:ManualMappingCuration	2023-03-17
EFO:1001983	Autosomal recessive Charcot Marie Tooth disease type 2X	skos:exactMatch	DOID:0110176	Charcot-Marie-Tooth disease axonal type 2X	semapv:ManualMappingCuration	2022-01-24
EFO:1001984	cardiac amyloidosis	skos:exactMatch	DOID:9000299	cardiac amyloidosis	semapv:ManualMappingCuration	2023-12-04
EFO:1001985	congenital fibrosis of the extraocular muscles	skos:exactMatch	DOID:0080143	congenital fibrosis of the extraocular muscles	semapv:ManualMappingCuration	2022-01-24
EFO:1001986	connective tissue disease	skos:exactMatch	DOID:65	connective tissue disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001987	dropped head syndrome	skos:exactMatch	DOID:0060034	dropped head syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1001988	Juvenile Polymyositis	skos:exactMatch	DOID:0080745	polymyositis	semapv:ManualMappingCuration	2023-12-04
EFO:1001989	Monomelic amyotrophy	skos:exactMatch	DOID:9007330	Monomelic Amyotrophy	semapv:ManualMappingCuration	2023-12-04
EFO:1001990	ocular motility disease	skos:exactMatch	DOID:1279	ocular motility disease	semapv:ManualMappingCuration	2022-01-24
EFO:1001991	pneumonitis	skos:exactMatch	DOID:552	pneumonia	semapv:ManualMappingCuration	2023-12-04
EFO:1001992	Scapuloperoneal spinal muscular atrophy	skos:exactMatch	DOID:0111552	scapuloperoneal spinal muscular atrophy	semapv:ManualMappingCuration	2022-01-24
EFO:1001993	scleroderma	skos:exactMatch	DOID:419	scleroderma	semapv:ManualMappingCuration	2022-01-24
EFO:1001994	Scleroderma Polymyositis Overlap Syndrome	skos:exactMatch	DOID:0080745	polymyositis	semapv:ManualMappingCuration	2023-12-04
EFO:1001995	Sclerodermatomyositis	skos:exactMatch	DOID:10223	dermatomyositis	semapv:ManualMappingCuration	2023-12-04
EFO:1001996	Thalassemia	skos:exactMatch	DOID:10241	thalassemia	semapv:ManualMappingCuration	2022-01-24
EFO:1001998	complex regional pain syndrome	skos:exactMatch	DOID:3223	complex regional pain syndrome	semapv:ManualMappingCuration	2022-01-24
EFO:1001999	systemic juvenile idiopathic arthritis	skos:exactMatch	DOID:9002765	Systemic Juvenile Rheumatoid Arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:1002000	Takotsubo cardiomyopathy	skos:exactMatch	DOID:9002399	Takotsubo Cardiomyopathy	semapv:ManualMappingCuration	2023-12-04
EFO:1002001	core binding factor acute myeloid leukemia	skos:exactMatch	DOID:0080796	core binding factor acute myeloid leukemia	semapv:ManualMappingCuration	2023-12-04
EFO:1002002	high altitude pulmonary edema	skos:exactMatch	DOID:9005526	Pulmonary Edema of Mountaineers	semapv:ManualMappingCuration	2023-12-04
EFO:1002003	hypersensitivity reaction disease	skos:exactMatch	DOID:0060056	hypersensitivity reaction disease	semapv:ManualMappingCuration	2022-01-24
EFO:1002004	drug hypersensitivity syndrome	skos:exactMatch	DOID:9007806	Drug Hypersensitivity Syndrome	semapv:ManualMappingCuration	2023-12-04
EFO:1002005	lumbar disc herniation	skos:exactMatch	DOID:9000585	Intervertebral Disc Disease	semapv:ManualMappingCuration	2023-12-04
EFO:1002006	treatment-resistant hypertension	skos:exactMatch	DOID:9006738	Hypertension Resistant to Conventional Therapy	semapv:ManualMappingCuration	2023-12-04
EFO:1002008	atypical teratoid rhabdoid tumor	skos:exactMatch	DOID:2129	atypical teratoid rhabdoid tumor	semapv:ManualMappingCuration	2022-01-24
EFO:1002010	TP53 Positive Breast Carcinoma	skos:exactMatch	DOID:3459	breast carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1002011	adult onset asthma	skos:exactMatch	DOID:2841	asthma	semapv:ManualMappingCuration	2023-12-04
EFO:1002012	ligament rupture	skos:exactMatch	DOID:9007994	ligament rupture	semapv:ManualMappingCuration	2023-12-04
EFO:1002013	alcoholic pancreatitis	skos:exactMatch	DOID:4988	alcoholic pancreatitis	semapv:ManualMappingCuration	2022-01-24
EFO:1002014	melancholia	skos:exactMatch	DOID:1595	melancholic depression	semapv:ManualMappingCuration	2023-12-04
EFO:1002014	melancholia	skos:exactMatch	DOID:2848	melancholia	semapv:ManualMappingCuration	2022-01-24
EFO:1002015	HPV-associated cervical carcinoma	skos:exactMatch	DOID:2893	cervix carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1002016	poorly differentiated follicular thyroid carcinoma	skos:exactMatch	DOID:3962	follicular thyroid carcinoma	semapv:ManualMappingCuration	2023-12-04
EFO:1002017	differentiated thyroid carcinoma	skos:exactMatch	DOID:0080525	differentiated high-grade thyroid carcinoma	semapv:ManualMappingCuration	2022-01-24
EFO:1002018	bronchial disease	skos:exactMatch	DOID:1176	bronchial disease	semapv:ManualMappingCuration	2022-01-24
EFO:1002019	oligoarticular juvenile idiopathic arthritis	skos:exactMatch	DOID:9008276	Juvenile Pauciarticular Chronic Arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:1002020	polyarticular juvenile idiopathic arthritis, rheumatoid factor negative	skos:exactMatch	DOID:676	juvenile rheumatoid arthritis	semapv:ManualMappingCuration	2023-12-04
EFO:1002021	ankle injury	skos:exactMatch	DOID:9001714	Ankle Injuries	semapv:ManualMappingCuration	2023-12-04
EFO:1002022	Herpes simplex infection	skos:exactMatch	DOID:8566	herpes simplex	semapv:ManualMappingCuration	2022-01-24
EFO:1002023	plantar wart	skos:exactMatch	DOID:13775	plantar wart	semapv:ManualMappingCuration	2022-01-24
EFO:1002024	streptococcal pharyngitis	skos:exactMatch	DOID:9000370	streptococcal pharyngitis	semapv:ManualMappingCuration	2023-12-04
EFO:1002025	measles	skos:exactMatch	DOID:8622	measles	semapv:ManualMappingCuration	2022-01-24
EFO:1002026	rubella	skos:exactMatch	DOID:8781	rubella	semapv:ManualMappingCuration	2022-01-24
EFO:1002027	osteomalacia	skos:exactMatch	DOID:10573	osteomalacia	semapv:ManualMappingCuration	2023-12-04
EFO:1002028	cicatricial alopecia	skos:exactMatch	DOID:9007442	Central Centrifugal Cicatricial Alopecia	semapv:ManualMappingCuration	2023-12-04
EFO:1002029	chronic rhinosinusitis with nasal polyps	skos:exactMatch	DOID:9007575	chronic rhinosinusitis with nasal polyps	semapv:ManualMappingCuration	2023-12-04
EFO:1002030	chronic rhinosinusitis without nasal polyps	skos:exactMatch	DOID:9006771	Chronic Rhinosinusitis	semapv:ManualMappingCuration	2023-12-04
EFO:1002031	Hodgkins lymphoma, mixed cellularity	skos:exactMatch	DOID:8654	Hodgkin's lymphoma, mixed cellularity	semapv:ManualMappingCuration	2022-01-24
EFO:1002034	secondary hypertension	skos:exactMatch	DOID:11130	secondary hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:1002039	renal hypertension	skos:exactMatch	DOID:1073	renal hypertension	semapv:ManualMappingCuration	2022-01-24
EFO:1002040	Corneal astigmatism	skos:exactMatch	DOID:11782	astigmatism	semapv:ManualMappingCuration	2023-12-04
EFO:1002046	apocrine sweat gland disease	skos:exactMatch	DOID:1383	sweat gland disease	semapv:ManualMappingCuration	2023-12-04
EFO:1002047	spotted fever	skos:exactMatch	DOID:11104	spotted fever	semapv:ManualMappingCuration	2022-01-24
EFO:1002048	kidney failure	skos:exactMatch	DOID:1074	kidney failure	semapv:ManualMappingCuration	2022-01-24
EFO:1002049	glomerular disease	skos:exactMatch	DOID:9000104	Glomerular Diseases	semapv:ManualMappingCuration	2023-12-04
EFO:1002050	nephritis	skos:exactMatch	DOID:10952	nephritis	semapv:ManualMappingCuration	2022-01-24
EFO:1002051	facial nerve disease	skos:exactMatch	DOID:1756	facial nerve disease	semapv:ManualMappingCuration	2022-01-24
HP:0000011	Neurogenic bladder	skos:exactMatch	DOID:12143	neurogenic bladder	semapv:ManualMappingCuration	2023-03-17
HP:0000175	Cleft palate	skos:exactMatch	DOID:674	cleft palate	semapv:ManualMappingCuration	2023-03-17
HP:0000407	Sensorineural hearing impairment	skos:exactMatch	DOID:10003	sensorineural hearing loss	semapv:ManualMappingCuration	2023-03-17
HP:0000483	Astigmatism	skos:exactMatch	DOID:11782	astigmatism	semapv:ManualMappingCuration	2023-03-17
HP:0000483	Astigmatism	skos:exactMatch	DOID:9835	refractive error	semapv:ManualMappingCuration	2023-03-17
HP:0000545	Myopia	skos:exactMatch	DOID:11830	myopia	semapv:ManualMappingCuration	2023-03-17
HP:0000979	Purpura	skos:exactMatch	DOID:3326	purpura	semapv:ManualMappingCuration	2023-03-17
HP:0000999	Pyoderma	skos:exactMatch	DOID:4223	pyoderma	semapv:ManualMappingCuration	2023-03-17
HP:0001636	Tetralogy of Fallot	skos:exactMatch	DOID:6419	tetralogy of Fallot	semapv:ManualMappingCuration	2023-03-17
HP:0001657	Prolonged QT interval	skos:exactMatch	DOID:2843	long QT syndrome	semapv:ManualMappingCuration	2023-03-17
HP:0001891	Iron deficiency anemia	skos:exactMatch	DOID:11758	iron deficiency anemia	semapv:ManualMappingCuration	2023-03-17
HP:0001915	Aplastic anemia	skos:exactMatch	DOID:12449	aplastic anemia	semapv:ManualMappingCuration	2023-03-17
HP:0001943	Hypoglycemia	skos:exactMatch	DOID:9993	hypoglycemia	semapv:ManualMappingCuration	2023-03-17
HP:0002014	Diarrhea	skos:exactMatch	DOID:13250	diarrhea	semapv:ManualMappingCuration	2023-03-17
HP:0002035	Rectal prolapse	skos:exactMatch	DOID:9307	rectal prolapse	semapv:ManualMappingCuration	2023-03-17
HP:0002110	Bronchiectasis	skos:exactMatch	DOID:9563	bronchiectasis	semapv:ManualMappingCuration	2023-03-17
HP:0002148	Hypophosphatemia	skos:exactMatch	DOID:0050336	hypophosphatemia	semapv:ManualMappingCuration	2023-03-17
HP:0002251	Aganglionic megacolon	skos:exactMatch	DOID:11372	megacolon	semapv:ManualMappingCuration	2023-03-17
HP:0002619	Varicose veins	skos:exactMatch	DOID:799	varicose veins	semapv:ManualMappingCuration	2023-03-17
HP:0002900	Hypokalemia	skos:exactMatch	DOID:4500	hypokalemia	semapv:ManualMappingCuration	2023-03-17
HP:0003072	Hypercalcemia	skos:exactMatch	DOID:12678	hypercalcemia	semapv:ManualMappingCuration	2023-03-17
HP:0003074	Hyperglycemia	skos:exactMatch	DOID:4195	hyperglycemia	semapv:ManualMappingCuration	2023-03-17
HP:0004840	Hypochromic microcytic anemia	skos:exactMatch	DOID:0050642	hypochromic microcytic anemia	semapv:ManualMappingCuration	2023-03-17
HP:0006536	Airway obstruction	skos:exactMatch	DOID:2320	obstructive lung disease	semapv:ManualMappingCuration	2023-03-17
HP:0007313	Cerebral degeneration	skos:exactMatch	DOID:1443	cerebral degeneration	semapv:ManualMappingCuration	2023-03-17
HP:0010865	Oppositional defiant disorder	skos:exactMatch	DOID:0050856	oppositional defiant disorder	semapv:ManualMappingCuration	2023-03-17
HP:0011950	Bronchiolitis	skos:exactMatch	DOID:2942	bronchiolitis	semapv:ManualMappingCuration	2023-03-17
HP:0012115	Hepatitis	skos:exactMatch	DOID:2237	hepatitis	semapv:ManualMappingCuration	2023-03-17
HP:0012234	Agranulocytosis	skos:exactMatch	DOID:12987	agranulocytosis	semapv:ManualMappingCuration	2023-03-17
HP:0030151	Cholangitis	skos:exactMatch	DOID:9446	cholangitis	semapv:ManualMappingCuration	2023-03-17
HP:0100727	Histiocytosis	skos:exactMatch	DOID:3405	histiocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000009	inherited bleeding disorder, platelet-type	skos:exactMatch	DOID:2218	blood platelet disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000023	infantile liver failure	skos:exactMatch	DOID:0080716	infantile liver failure syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0000032	febrile seizures, familial	skos:exactMatch	DOID:0111297	familial febrile seizures	semapv:ManualMappingCuration	2023-03-17
MONDO:0000050	isolated congenital growth hormone deficiency	skos:exactMatch	DOID:0060870	isolated growth hormone deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000062	isolated microphthalmia	skos:exactMatch	DOID:0080637	isolated microphthalmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000079	nephrolithiasis/osteoporosis, hypophosphatemic	skos:exactMatch	DOID:0080655	hypophosphatemic nephrolithiasis/osteoporosis	semapv:ManualMappingCuration	2024-02-18
MONDO:0000087	polymicrogyria	skos:exactMatch	DOID:0080918	polymicrogyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0000127	geleophysic dysplasia	skos:exactMatch	DOID:0111724	geleophysic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000133	immunodeficiency-centromeric instability-facial anomalies syndrome	skos:exactMatch	DOID:0090007	immunodeficiency-centromeric instability-facial anomalies syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000136	keratosis follicularis spinulosa decalvans	skos:exactMatch	DOID:0080753	keratosis follicularis spinulosa decalvans	semapv:ManualMappingCuration	2023-03-17
MONDO:0000141	mosaic variegated aneuploidy syndrome	skos:exactMatch	DOID:0080688	mosaic variegated aneuploidy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000160	epilepsy, familial adult myoclonic	skos:exactMatch	DOID:0111689	familial adult myoclonic epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000171	muscular dystrophy-dystroglycanopathy, type A	skos:exactMatch	DOID:0050560	Walker-Warburg syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000172	muscular dystrophy-dystroglycanopathy, type B	skos:exactMatch	DOID:0112375	muscular dystrophy-dystroglycanopathy type B	semapv:ManualMappingCuration	2023-06-18
MONDO:0000193	cortisone reductase deficiency	skos:exactMatch	DOID:0090139	cortisone reductase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000214	hypermanganesemia with dystonia	skos:exactMatch	DOID:0080535	hypermanganesemia with dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000224	acquired carbohydrate metabolism disease	skos:exactMatch	DOID:0050013	carbohydrate metabolism disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0000236	oropharyngeal anthrax	skos:exactMatch	DOID:0050059	oropharyngeal anthrax	semapv:ManualMappingCuration	2024-04-21
MONDO:0000252	inflammatory diarrhea	skos:exactMatch	DOID:0050132	inflammatory diarrhea	semapv:ManualMappingCuration	2023-03-17
MONDO:0000254	cutaneous mycosis	skos:exactMatch	DOID:0050134	cutaneous mycosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000255	subcutaneous mycosis	skos:exactMatch	DOID:0050135	subcutaneous mycosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000256	systemic mycosis	skos:exactMatch	DOID:0050136	systemic mycosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000257	acute diarrhea	skos:exactMatch	DOID:0050140	acute diarrhea	semapv:ManualMappingCuration	2023-03-17
MONDO:0000262	otomycosis	skos:exactMatch	DOID:0050147	otomycosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000263	laryngotracheitis	skos:exactMatch	DOID:0050148	laryngotracheitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000271	tuberculous salpingitis	skos:exactMatch	DOID:0050166	tuberculous salpingitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000286	Epstein-Barr virus hepatitis	skos:exactMatch	DOID:0050204	Epstein-Barr virus hepatitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000307	parasitic Ichthyosporea infectious disease	skos:exactMatch	DOID:0050291	parasitic Ichthyosporea infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000308	primary systemic mycosis	skos:exactMatch	DOID:0050292	primary systemic mycosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000313	hypophosphatemia	skos:exactMatch	DOID:0050336	hypophosphatemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0000314	primary bacterial infectious disease	skos:exactMatch	DOID:0050338	primary bacterial infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000315	commensal bacterial infectious disease	skos:exactMatch	DOID:0050339	commensal bacterial infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000316	opportunistic bacterial infectious disease	skos:exactMatch	DOID:0050340	opportunistic bacterial infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000320	glandular tularemia	skos:exactMatch	DOID:0050382	glandular tularemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0000327	Buruli ulcer disease	skos:exactMatch	DOID:0050456	Buruli ulcer disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000328	hyperphosphatemia	skos:exactMatch	DOID:0050459	hyperphosphatemia	semapv:ManualMappingCuration	2024-02-18
MONDO:0000334	multinodular goiter	skos:exactMatch	DOID:0050489	multinodular goiter	semapv:ManualMappingCuration	2023-03-17
MONDO:0000341	paralytic poliomyelitis	skos:exactMatch	DOID:0050515	paralytic poliomyelitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000351	disorder of methionine catabolism	skos:exactMatch	DOID:0050544	hypermethioninemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000355	Ullrich congenital muscular dystrophy	skos:exactMatch	DOID:0050558	Ullrich congenital muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000358	orofacial cleft	skos:exactMatch	DOID:0050567	orofacial cleft	semapv:ManualMappingCuration	2023-03-17
MONDO:0000359	spondylocostal dysostosis	skos:exactMatch	DOID:0050568	spondylocostal dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000368	extrapulmonary tuberculosis	skos:exactMatch	DOID:0050598	extrapulmonary tuberculosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000369	abdominal tuberculosis	skos:exactMatch	DOID:0050599	abdominal tuberculosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000371	oral cavity carcinoma in situ	skos:exactMatch	DOID:0050610	oral cavity carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0000372	pharynx carcinoma in situ	skos:exactMatch	DOID:0050611	pharynx carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0000373	gall bladder carcinoma in situ	skos:exactMatch	DOID:0050612	gallbladder carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0000374	bile duct carcinoma in situ	skos:exactMatch	DOID:0050613	bile duct carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0000375	bronchus carcinoma in situ	skos:exactMatch	DOID:0050614	bronchus carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0000376	respiratory system cancer	skos:exactMatch	DOID:0050615	respiratory system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000380	paranasal sinus carcinoma	skos:exactMatch	DOID:0050619	paranasal sinus cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000381	infiltrating renal pelvis transitional cell carcinoma	skos:exactMatch	DOID:0050620	infiltrating renal pelvis transitional cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000382	respiratory system benign neoplasm	skos:exactMatch	DOID:0050621	respiratory system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000383	benign reproductive system neoplasm	skos:exactMatch	DOID:0050622	reproductive organ benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000384	bladder benign neoplasm	skos:exactMatch	DOID:0050623	bladder benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0000385	benign digestive system neoplasm	skos:exactMatch	DOID:0050624	gastrointestinal system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000386	digestive system neuroendocrine tumor, grade 1/2	skos:exactMatch	DOID:0050626	gastrointestinal neuroendocrine tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0000387	hypochromic microcytic anemia	skos:exactMatch	DOID:0050642	hypochromic microcytic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000389	atelosteogenesis	skos:exactMatch	DOID:0050648	atelosteogenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000390	vitelliform macular dystrophy	skos:exactMatch	DOID:0050661	vitelliform macular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000396	spastic cerebral palsy	skos:exactMatch	DOID:0050669	spastic cerebral palsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000397	ataxic cerebral palsy	skos:exactMatch	DOID:0050670	ataxic cerebral palsy	semapv:ManualMappingCuration	2024-04-21
MONDO:0000405	anal canal cancer	skos:exactMatch	DOID:0050688	anal canal cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0000407	malignant pleural solitary fibrous tumor	skos:exactMatch	DOID:0050695	malignant pleural solitary fibrous tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0000411	electroclinical syndrome	skos:exactMatch	DOID:0050701	electroclinical syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000412	neonatal period electroclinical syndrome	skos:exactMatch	DOID:0050702	neonatal period electroclinical syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000413	infancy electroclinical syndrome	skos:exactMatch	DOID:0050703	infancy electroclinical syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000414	childhood electroclinical syndrome	skos:exactMatch	DOID:0050704	childhood electroclinical syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000415	adolescence-adult electroclinical syndrome	skos:exactMatch	DOID:0050705	adolescence-adult electroclinical syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000421	inborn serine deficiency	skos:exactMatch	DOID:0050721	serine deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000424	inborn vitamin B12 deficiency	skos:exactMatch	DOID:0050731	vitamin B12 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000425	X-linked disease	skos:exactMatch	DOID:0050735	X-linked monogenic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000426	autosomal dominant disease	skos:exactMatch	DOID:0050736	autosomal dominant disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000429	autosomal genetic disease	skos:exactMatch	DOID:0050739	autosomal genetic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000430	mature T-cell and NK-cell non-Hodgkin lymphoma	skos:exactMatch	DOID:0050743	mature T-cell and NK-cell lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000430	mature T-cell and NK-cell non-Hodgkin lymphoma	skos:exactMatch	DOID:0050749	peripheral T-cell lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000432	lymphoplasmacytic lymphoma	skos:exactMatch	DOID:0050747	lymphoplasmacytic lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000437	cerebellar ataxia	skos:exactMatch	DOID:0050753	cerebellar ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000440	metabolic acidosis	skos:exactMatch	DOID:0050758	metabolic acidosis	semapv:ManualMappingCuration	2023-11-19
MONDO:0000447	autosomal dominant polycystic liver disease	skos:exactMatch	DOID:0050770	polycystic liver disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000453	short QT syndrome	skos:exactMatch	DOID:0050793	short QT syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000455	cone dystrophy	skos:exactMatch	DOID:0050795	cone dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000456	cerebral creatine deficiency syndrome	skos:exactMatch	DOID:0050798	cerebral creatine deficiency syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000461	nutritional biotin deficiency	skos:exactMatch	DOID:0050810	biotin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000463	Ochoa syndrome	skos:exactMatch	DOID:0050816	urofacial syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000465	atrioventricular block	skos:exactMatch	DOID:0050820	atrioventricular block	semapv:ManualMappingCuration	2023-03-17
MONDO:0000468	third-degree atrioventricular block	skos:exactMatch	DOID:0050823	third-degree atrioventricular block	semapv:ManualMappingCuration	2023-03-17
MONDO:0000469	sinoatrial node disorder	skos:exactMatch	DOID:0050824	sinoatrial node disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000470	endocardium disorder	skos:exactMatch	DOID:0050825	endocardium disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000473	arterial disorder	skos:exactMatch	DOID:0050828	artery disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000474	pericardium disorder	skos:exactMatch	DOID:0050829	pericardium disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000476	generalized dystonia	skos:exactMatch	DOID:0050835	generalized dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000477	focal dystonia	skos:exactMatch	DOID:0050836	focal dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000478	multifocal dystonia	skos:exactMatch	DOID:0050837	multifocal dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000481	cervical dystonia	skos:exactMatch	DOID:0050840	cervical dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000483	oculogyric crisis	skos:exactMatch	DOID:0050842	oculogyric crisis	semapv:ManualMappingCuration	2023-11-19
MONDO:0000485	spasmodic dystonia	skos:exactMatch	DOID:0050844	spasmodic dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000486	craniofacial dystonia	skos:exactMatch	DOID:0050845	cranio-facial dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000489	diabetic encephalopathy	skos:exactMatch	DOID:0050850	diabetic encephalopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000490	glomerulosclerosis	skos:exactMatch	DOID:0050851	glomerulosclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000491	limb ischemia	skos:exactMatch	DOID:0050852	limb ischemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0000496	hemorrhagic cystitis	skos:exactMatch	DOID:0050859	hemorrhagic cystitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000497	pyometritis	skos:exactMatch	DOID:0050862	pyometritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000502	villous adenoma	skos:exactMatch	DOID:0050869	villous adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000503	lung adenocarcinoma in situ	skos:exactMatch	DOID:0050870	pulmonary adenocarcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0000507	inclusion body myopathy with Paget disease of bone and frontotemporal dementia	skos:exactMatch	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000508	syndromic intellectual disability	skos:exactMatch	DOID:0050888	syndromic intellectual disability	semapv:ManualMappingCuration	2023-03-17
MONDO:0000509	non-syndromic intellectual disability	skos:exactMatch	DOID:0050889	non-syndromic intellectual disability	semapv:ManualMappingCuration	2023-03-17
MONDO:0000513	bone ameloblastoma	skos:exactMatch	DOID:0050895	bone ameloblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000514	bone squamous cell carcinoma	skos:exactMatch	DOID:0050896	bone squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000515	bone chondrosarcoma	skos:exactMatch	DOID:0050897	bone chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000517	brain stem medulloblastoma	skos:exactMatch	DOID:0050899	brain stem medulloblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000521	salivary gland carcinoma	skos:exactMatch	DOID:0050904	salivary gland carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000524	mixed extragonadal germ cell cancer	skos:exactMatch	DOID:0050907	mixed extragonadal germ cell cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000527	colon adenoma	skos:exactMatch	DOID:0050912	colon adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000530	rectum adenoma	skos:exactMatch	DOID:0050915	rectal adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000531	bronchus mucoepidermoid carcinoma	skos:exactMatch	DOID:0050916	bronchus mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000532	lung combined type small cell adenocarcinoma	skos:exactMatch	DOID:0050917	lung combined type small cell adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000534	trachea mucoepidermoid carcinoma	skos:exactMatch	DOID:0050919	trachea mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000540	small intestinal neuroendocrine tumor G1	skos:exactMatch	DOID:0050925	small intestine carcinoid neuroendocrine tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0000541	jejunal adenocarcinoma	skos:exactMatch	DOID:0050926	jejunal adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000543	ovarian melanoma	skos:exactMatch	DOID:0050928	ovarian melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000544	mucosal melanoma	skos:exactMatch	DOID:0050929	mucosal melanoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000545	sublingual gland adenoid cystic carcinoma	skos:exactMatch	DOID:0050930	sublingual gland adenoid cystic carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000548	ovarian clear cell cancer	skos:exactMatch	DOID:0050934	ovarian clear cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000549	cervical neuroblastoma	skos:exactMatch	DOID:0050935	cervical neuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000551	retroperitoneal neuroblastoma	skos:exactMatch	DOID:0050937	retroperitoneal neuroblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000553	uterine corpus endometrial carcinoma	skos:exactMatch	DOID:0050939	uterine corpus endometrial carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000554	endocervical adenocarcinoma	skos:exactMatch	DOID:0050940	endocervical adenocarcinoma	semapv:ManualMappingCuration	2023-08-20
MONDO:0000565	infective endocarditis	skos:exactMatch	DOID:0060000	infective endocarditis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000569	autoimmune disorder of endocrine system	skos:exactMatch	DOID:0060005	autoimmune disease of endocrine system	semapv:ManualMappingCuration	2023-03-17
MONDO:0000572	recombinase activating gene 1 deficiency	skos:exactMatch	DOID:0060011	recombinase activating gene 1 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000573	recombinase activating gene 2 deficiency	skos:exactMatch	DOID:0060012	recombinase activating gene 2 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000586	autoimmune disorder of exocrine system	skos:exactMatch	DOID:0060029	autoimmune disease of exocrine system	semapv:ManualMappingCuration	2023-03-17
MONDO:0000587	autoimmune disease of ear, nose and throat	skos:exactMatch	DOID:0060030	autoimmune disease of eyes, ear, nose and throat	semapv:ManualMappingCuration	2023-03-17
MONDO:0000588	autoimmune disorder of gastrointestinal tract	skos:exactMatch	DOID:0060031	autoimmune disease of gastrointestinal tract	semapv:ManualMappingCuration	2023-03-17
MONDO:0000589	autoimmune disorder of musculoskeletal system	skos:exactMatch	DOID:0060032	autoimmune disease of musculoskeletal system	semapv:ManualMappingCuration	2023-03-17
MONDO:0000590	autoimmune disorder of peripheral nervous system	skos:exactMatch	DOID:0060033	autoimmune disease of peripheral nervous system	semapv:ManualMappingCuration	2023-03-17
MONDO:0000591	intrinsic cardiomyopathy	skos:exactMatch	DOID:0060036	intrinsic cardiomyopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000592	specific developmental disorder	skos:exactMatch	DOID:0060038	specific developmental disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0000594	pervasive developmental disorder	skos:exactMatch	DOID:0060040	pervasive developmental disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0000595	sexual and gender identity disorders	skos:exactMatch	DOID:0060043	sexual health disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0000602	autoimmune disorder of blood	skos:exactMatch	DOID:0060050	autoimmune disease of blood	semapv:ManualMappingCuration	2023-03-17
MONDO:0000603	autoimmune disorder of cardiovascular system	skos:exactMatch	DOID:0060051	autoimmune disease of cardiovascular system	semapv:ManualMappingCuration	2023-03-17
MONDO:0000608	familial juvenile hyperuricemic nephropathy	skos:exactMatch	DOID:0060062	familial juvenile hyperuricemic nephropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000611	pre-malignant neoplasm	skos:exactMatch	DOID:0060071	pre-malignant neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000612	lymphatic system cancer	skos:exactMatch	DOID:0060073	lymphatic system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000620	breast benign neoplasm	skos:exactMatch	DOID:0060082	breast benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000621	immune system cancer	skos:exactMatch	DOID:0060083	immune system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000624	benign female reproductive system neoplasm	skos:exactMatch	DOID:0060086	female reproductive organ benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000625	benign male reproductive system neoplasm	skos:exactMatch	DOID:0060087	male reproductive organ benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000626	vestibular gland benign neoplasm	skos:exactMatch	DOID:0060088	vestibular gland benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0000627	benign endocrine neoplasm	skos:exactMatch	DOID:0060089	endocrine organ benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000628	central nervous system organ benign neoplasm	skos:exactMatch	DOID:0060090	central nervous system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000629	cardiovascular organ benign neoplasm	skos:exactMatch	DOID:0060091	cardiovascular organ benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000630	immune system organ benign neoplasm	skos:exactMatch	DOID:0060092	immune system organ benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0000631	bone benign neoplasm	skos:exactMatch	DOID:0060094	bone benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000632	uterine benign neoplasm	skos:exactMatch	DOID:0060095	uterine benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000633	sensory organ benign neoplasm	skos:exactMatch	DOID:0060096	sensory organ benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000634	thoracic benign neoplasm	skos:exactMatch	DOID:0060097	thoracic benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000636	musculoskeletal system benign neoplasm	skos:exactMatch	DOID:0060099	musculoskeletal system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000637	musculoskeletal system cancer	skos:exactMatch	DOID:0060100	musculoskeletal system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000638	benign glioma	skos:exactMatch	DOID:0060101	benign glioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000640	central nervous system primitive neuroectodermal neoplasm	skos:exactMatch	DOID:0060103	central nervous system embryonal tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0000643	vulvar benign neoplasm	skos:exactMatch	DOID:0060109	vulvar benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000644	cervical benign neoplasm	skos:exactMatch	DOID:0060110	cervical benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0000645	fallopian tube benign neoplasm	skos:exactMatch	DOID:0060111	fallopian tube benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0000647	benign vaginal neoplasm	skos:exactMatch	DOID:0060114	vaginal benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000648	nervous system benign neoplasm	skos:exactMatch	DOID:0060115	nervous system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000649	sensory system cancer	skos:exactMatch	DOID:0060116	sensory system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000650	peritoneal benign neoplasm	skos:exactMatch	DOID:0060117	peritoneal benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000652	integumentary system benign neoplasm	skos:exactMatch	DOID:0060121	integumentary system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000653	integumentary system cancer	skos:exactMatch	DOID:0060122	integumentary system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000654	benign connective and soft tissue neoplasm	skos:exactMatch	DOID:0060123	connective tissue benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000661	alexithymia	skos:exactMatch	DOID:0060131	alexithymia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000665	apraxia	skos:exactMatch	DOID:0060135	apraxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000666	associative visual agnosia	skos:exactMatch	DOID:0060136	associative agnosia	semapv:ManualMappingCuration	2024-04-21
MONDO:0000667	auditory agnosia	skos:exactMatch	DOID:0060137	auditory agnosia	semapv:ManualMappingCuration	2024-04-21
MONDO:0000685	visual agnosia	skos:exactMatch	DOID:0060155	visual agnosia	semapv:ManualMappingCuration	2024-04-21
MONDO:0000688	inborn organic aciduria	skos:exactMatch	DOID:0060159	organic acidemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000698	gamma-amino butyric acid metabolism disorder	skos:exactMatch	DOID:0060176	gamma-amino butyric acid metabolism disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0000700	familial hemiplegic migraine	skos:exactMatch	DOID:0060178	familial hemiplegic migraine	semapv:ManualMappingCuration	2023-03-17
MONDO:0000701	ischemic colitis	skos:exactMatch	DOID:0060181	ischemic colitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000708	Crohn jejunoileitis	skos:exactMatch	DOID:0060188	jejunoileitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000709	Crohn ileitis	skos:exactMatch	DOID:0060189	ileitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000710	gastroduodenal Crohn disease	skos:exactMatch	DOID:0060191	gastroduodenal Crohn's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0000715	lymph node adenoid cystic carcinoma	skos:exactMatch	DOID:0060219	lymph node adenoid cystic carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000722	non-syndromic synpolydactyly	skos:exactMatch	DOID:0060242	synpolydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0000723	stutter disorder	skos:exactMatch	DOID:0060243	stuttering	semapv:ManualMappingCuration	2023-11-19
MONDO:0000726	idiopathic scoliosis	skos:exactMatch	DOID:0060250	idiopathic scoliosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000727	scapuloperoneal myopathy	skos:exactMatch	DOID:0060253	scapuloperoneal myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000728	ptosis	skos:exactMatch	DOID:0060260	ptosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000732	combined oxidative phosphorylation deficiency	skos:exactMatch	DOID:0060286	combined oxidative phosphorylation deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000733	cornea plana	skos:exactMatch	DOID:0060287	cornea plana	semapv:ManualMappingCuration	2023-03-17
MONDO:0000734	Ohdo syndrome and variants	skos:exactMatch	DOID:0060289	Ohdo syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000736	dyschromatosis universalis hereditaria	skos:exactMatch	DOID:0060304	dyschromatosis universalis hereditaria	semapv:ManualMappingCuration	2023-03-17
MONDO:0000761	syndrome caused by partial chromosomal deletion	skos:exactMatch	DOID:0060388	chromosomal deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000762	syndrome caused by partial chromosomal duplication	skos:exactMatch	DOID:0060429	chromosomal duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000763	epithelial and subepithelial corneal dystrophy	skos:exactMatch	DOID:0060440	epithelial and subepithelial dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000764	epithelial-stromal TGFBI dystrophy	skos:exactMatch	DOID:0060441	epithelial-stromal TGFBI dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000766	corneal endothelial dystrophy	skos:exactMatch	DOID:0060443	corneal endothelial dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000771	allergic respiratory disease	skos:exactMatch	DOID:0060496	respiratory allergy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000774	autoimmune neuropathy	skos:exactMatch	DOID:0040087	autoimmune peripheral neuropathy	semapv:ManualMappingCuration	2024-04-21
MONDO:0000774	autoimmune neuropathy	skos:exactMatch	DOID:0060499	autoimmune neuropathy	semapv:ManualMappingCuration	2024-04-21
MONDO:0000777	gastrointestinal allergy	skos:exactMatch	DOID:0060502	gastrointestinal allergy	semapv:ManualMappingCuration	2024-04-21
MONDO:0000812	vertebral column disorder	skos:exactMatch	DOID:0060564	spinal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000816	abdominal obesity-metabolic syndrome	skos:exactMatch	DOID:0060611	abdominal obesity-metabolic syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000819	anencephaly	skos:exactMatch	DOID:0060668	anencephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0000820	cerebral cavernous malformation	skos:exactMatch	DOID:0060669	cerebral cavernous malformation	semapv:ManualMappingCuration	2023-03-17
MONDO:0000824	congenital diarrhea	skos:exactMatch	DOID:0060774	congenital diarrhea	semapv:ManualMappingCuration	2023-03-17
MONDO:0000827	salmonellosis	skos:exactMatch	DOID:0060859	salmonellosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000828	juvenile-onset Parkinson disease	skos:exactMatch	DOID:0060893	juvenile-onset Parkinson's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000831	thrombotic disease	skos:exactMatch	DOID:0060903	thrombosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000833	bone remodeling disease	skos:exactMatch	DOID:0080005	bone remodeling disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000836	disease of bone structure	skos:exactMatch	DOID:0080010	bone structure disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000837	bone resorption disease	skos:exactMatch	DOID:0080011	bone resorption disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000845	fibrous dysplasia	skos:exactMatch	DOID:0080031	fibrous dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000858	neuronal intestinal dysplasia	skos:exactMatch	DOID:0080072	intestinal pseudo-obstruction	semapv:ManualMappingCuration	2023-11-19
MONDO:0000863	myopathy, lactic acidosis, and sideroblastic anemia	skos:exactMatch	DOID:0080099	myopathy, lactic acidosis, and sideroblastic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000866	hereditary myoglobinuria	skos:exactMatch	DOID:0080108	myoglobinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0000870	childhood acute lymphoblastic leukemia	skos:exactMatch	DOID:0080144	childhood acute lymphocytic leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000873	lymphoblastic lymphoma	skos:exactMatch	DOID:0080147	lymphoblastic lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000879	cutaneous candidiasis	skos:exactMatch	DOID:0080161	cutaneous candidiasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000890	Zika virus congenital syndrome	skos:exactMatch	DOID:0080180	Zika virus congenital syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0000892	colon medullary carcinoma	skos:exactMatch	DOID:0080183	medullary colon carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000894	mucinous bronchioloalveolar adenocarcinoma	skos:exactMatch	DOID:0080185	mucinous bronchioloalveolar adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000902	agenesis of the corpus callosum with peripheral neuropathy	skos:exactMatch	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0000903	myoclonus-dystonia syndrome	skos:exactMatch	DOID:0090033	myoclonic dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0000904	complex cortical dysplasia with other brain malformations	skos:exactMatch	DOID:0090131	complex cortical dysplasia with other brain malformations	semapv:ManualMappingCuration	2023-03-17
MONDO:0000914	cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1	skos:exactMatch	DOID:0111035	CADASIL 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0000916	intestinal infectious disease	skos:exactMatch	DOID:100	intestinal infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000919	ampulla of vater cancer	skos:exactMatch	DOID:10020	ampulla of Vater cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000920	duodenum cancer	skos:exactMatch	DOID:10021	duodenum cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000921	ampulla of vater neoplasm	skos:exactMatch	DOID:10022	ampulla of Vater benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0000923	interstitial emphysema	skos:exactMatch	DOID:10030	pulmonary interstitial emphysema	semapv:ManualMappingCuration	2023-03-17
MONDO:0000924	compensatory emphysema	skos:exactMatch	DOID:10031	compensatory emphysema	semapv:ManualMappingCuration	2023-03-17
MONDO:0000926	eye accommodation disease	skos:exactMatch	DOID:10034	eye accommodation disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000928	eyelid melanoma	skos:exactMatch	DOID:10040	malignant eyelid melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000931	endometrial disorder	skos:exactMatch	DOID:1005	endometrial disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000934	laryngeal leiomyoma	skos:exactMatch	DOID:10070	larynx leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000935	larynx squamous papilloma	skos:exactMatch	DOID:10071	larynx squamous papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000936	syphilitic meningitis	skos:exactMatch	DOID:10073	syphilitic meningitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000937	syphilitic encephalitis	skos:exactMatch	DOID:10081	syphilitic encephalitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000938	gastric leiomyoma	skos:exactMatch	DOID:10087	gastric leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000944	cerebral artery occlusion	skos:exactMatch	DOID:10127	cerebral artery occlusion	semapv:ManualMappingCuration	2023-03-17
MONDO:0000945	venous insufficiency	skos:exactMatch	DOID:10128	venous insufficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0000947	psychosexual disorder	skos:exactMatch	DOID:10132	psychosexual disorder	semapv:ManualMappingCuration	2024-04-21
MONDO:0000949	conjunctival degeneration	skos:exactMatch	DOID:10139	conjunctival degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0000952	cancer of long bone of lower limb	skos:exactMatch	DOID:10149	long bones of lower limb cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000955	ileum cancer	skos:exactMatch	DOID:10153	ileum cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0000956	small intestine cancer	skos:exactMatch	DOID:10154	small intestine cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0000959	malignant hypertensive renal disease	skos:exactMatch	DOID:10177	malignant hypertensive renal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000962	spindle cell lipoma	skos:exactMatch	DOID:10184	spindle cell lipoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0000963	esophageal lipoma	skos:exactMatch	DOID:10187	esophageal lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000964	skin lipoma	skos:exactMatch	DOID:10188	skin lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000965	liver lipoma	skos:exactMatch	DOID:10190	liver lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000968	kidney lipoma	skos:exactMatch	DOID:10194	kidney lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000969	pleural lipoma	skos:exactMatch	DOID:10195	pleural lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000970	breast lipoma	skos:exactMatch	DOID:10199	breast lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000972	gallbladder lipoma	skos:exactMatch	DOID:10201	gallbladder lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000973	external ear lipoma	skos:exactMatch	DOID:10203	external ear lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000978	extrahepatic bile duct lipoma	skos:exactMatch	DOID:10209	extrahepatic bile duct lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000980	aortic atherosclerosis	skos:exactMatch	DOID:10230	aortic atherosclerosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000981	Histoplasma pericarditis	skos:exactMatch	DOID:10234	histoplasmosis pericarditis	semapv:ManualMappingCuration	2024-04-21
MONDO:0000988	discharging ear	skos:exactMatch	DOID:10261	otorrhea	semapv:ManualMappingCuration	2023-03-17
MONDO:0000992	heart conduction disease	skos:exactMatch	DOID:10273	heart conduction disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0000993	prostate squamous cell carcinoma	skos:exactMatch	DOID:10287	prostate squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0000995	familial periodic paralysis	skos:exactMatch	DOID:1029	familial periodic paralysis	semapv:ManualMappingCuration	2023-03-17
MONDO:0000996	prostate lymphoma	skos:exactMatch	DOID:10290	prostate lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001007	chronic meningitis	skos:exactMatch	DOID:10341	chronic meningitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001014	chronic leukemia	skos:exactMatch	DOID:1036	chronic leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001020	amblyopia	skos:exactMatch	DOID:10376	amblyopia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001023	prolymphocytic leukemia	skos:exactMatch	DOID:1039	prolymphocytic leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001024	pneumonic plague	skos:exactMatch	DOID:10398	pneumonic plague	semapv:ManualMappingCuration	2024-04-21
MONDO:0001028	acute pericementitis	skos:exactMatch	DOID:10423	acute pericementitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001029	Klippel-Feil syndrome	skos:exactMatch	DOID:10426	Klippel-Feil syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001031	purulent acute otitis media	skos:exactMatch	DOID:10435	purulent acute otitis media	semapv:ManualMappingCuration	2024-04-21
MONDO:0001039	tonsillitis	skos:exactMatch	DOID:10456	tonsillitis	semapv:ManualMappingCuration	2023-12-24
MONDO:0001040	nasopharyngitis	skos:exactMatch	DOID:10460	nasopharyngitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001042	patellar tendinitis	skos:exactMatch	DOID:10471	patellar tendinitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001045	intestinal atresia	skos:exactMatch	DOID:10486	intestinal atresia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001046	imperforate anus	skos:exactMatch	DOID:10488	imperforate anus	semapv:ManualMappingCuration	2024-06-23
MONDO:0001051	acute otitis externa	skos:exactMatch	DOID:10518	beach ear	semapv:ManualMappingCuration	2024-04-21
MONDO:0001052	chronic fungal otitis externa	skos:exactMatch	DOID:10519	chronic fungal otitis externa	semapv:ManualMappingCuration	2024-04-21
MONDO:0001056	gastric cancer	skos:exactMatch	DOID:10534	stomach cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001059	gastric lymphoma	skos:exactMatch	DOID:10540	gastric lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001063	cardia cancer	skos:exactMatch	DOID:10548	cardia cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001064	acute eustachian salpingitis	skos:exactMatch	DOID:10550	acute eustachian salpingitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001074	chronic tic disorder	skos:exactMatch	DOID:10600	chronic tic disorder	semapv:ManualMappingCuration	2024-04-21
MONDO:0001078	tropical sprue	skos:exactMatch	DOID:10607	tropical sprue	semapv:ManualMappingCuration	2023-03-17
MONDO:0001080	acute gonococcal cervicitis	skos:exactMatch	DOID:10615	acute gonococcal cervicitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001081	acute cervicitis	skos:exactMatch	DOID:10616	acute cervicitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001082	lymph node cancer	skos:exactMatch	DOID:10619	lymph node cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001083	Fanconi renotubular syndrome	skos:exactMatch	DOID:1062	Fanconi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001084	primary optic atrophy	skos:exactMatch	DOID:10627	primary optic atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001085	interstitial nephritis	skos:exactMatch	DOID:1063	interstitial nephritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001087	schizotypal personality disorder	skos:exactMatch	DOID:10646	schizotypal personality disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001090	acute anterolateral myocardial infarction	skos:exactMatch	DOID:10651	acute anterolateral myocardial infarction	semapv:ManualMappingCuration	2024-04-21
MONDO:0001091	lipoma of colon	skos:exactMatch	DOID:10655	lipoma of colon	semapv:ManualMappingCuration	2024-04-21
MONDO:0001092	colon leiomyoma	skos:exactMatch	DOID:10656	colon leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001093	colonic lymphangioma	skos:exactMatch	DOID:10657	colonic lymphangioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001096	mediastinum ganglioneuroblastoma	skos:exactMatch	DOID:10661	mediastinum ganglioneuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001104	toxic diffuse goiter	skos:exactMatch	DOID:10719	toxic diffuse goiter	semapv:ManualMappingCuration	2023-03-17
MONDO:0001108	broad ligament malignant neoplasm	skos:exactMatch	DOID:10744	broad ligament malignant neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0001110	chronic pyelonephritis	skos:exactMatch	DOID:1076	chronic pyelonephritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001112	bubonic plague	skos:exactMatch	DOID:10773	bubonic plague	semapv:ManualMappingCuration	2024-04-21
MONDO:0001114	bacterial myocarditis	skos:exactMatch	DOID:10779	septic myocarditis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001115	familial polycythemia	skos:exactMatch	DOID:10780	primary polycythemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001117	methemoglobinemia	skos:exactMatch	DOID:10783	methemoglobinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001122	chronic maxillary sinusitis	skos:exactMatch	DOID:10792	chronic maxillary sinusitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001123	chronic sphenoidal sinusitis	skos:exactMatch	DOID:10793	chronic sphenoidal sinusitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001128	nasal cavity cancer	skos:exactMatch	DOID:10811	nasal cavity cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001129	nasal cavity olfactory neuroblastoma	skos:exactMatch	DOID:10812	nasal cavity olfactory neuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001130	nasal cavity lymphoma	skos:exactMatch	DOID:10813	nasal cavity lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001134	essential hypertension	skos:exactMatch	DOID:10825	essential hypertension	semapv:ManualMappingCuration	2023-03-17
MONDO:0001146	fourth cranial nerve palsy	skos:exactMatch	DOID:10869	fourth cranial nerve palsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001147	meningocele	skos:exactMatch	DOID:1088	meningocele	semapv:ManualMappingCuration	2023-03-17
MONDO:0001149	microcephaly	skos:exactMatch	DOID:10907	microcephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0001152	amnestic disorder	skos:exactMatch	DOID:10914	amnestic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001157	dependent personality disorder	skos:exactMatch	DOID:10931	dependent personality disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001160	dissociative disorder	skos:exactMatch	DOID:10935	dissociative disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001161	schizoid personality disorder	skos:exactMatch	DOID:10936	schizoid personality disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001162	impulse control disorder	skos:exactMatch	DOID:10937	impulse control disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001163	paranoid personality disorder	skos:exactMatch	DOID:10938	paranoid personality disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001165	tongue disorder	skos:exactMatch	DOID:10944	tongue disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001169	spastic monoplegia	skos:exactMatch	DOID:10968	spastic monoplegia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001171	acute salpingo-oophoritis	skos:exactMatch	DOID:10971	acute salpingo-oophoritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001172	salpingo-oophoritis	skos:exactMatch	DOID:10972	salpingo-oophoritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001173	acute salpingitis	skos:exactMatch	DOID:10973	acute salpingitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001174	conjunctival vascular disorder	skos:exactMatch	DOID:10989	conjunctival vascular disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001182	idiopathic corneal edema	skos:exactMatch	DOID:11033	idiopathic corneal edema	semapv:ManualMappingCuration	2023-03-17
MONDO:0001184	chronic rapidly progressive glomerulonephritis	skos:exactMatch	DOID:11036	chronic rapidly progressive glomerulonephritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001185	dissociative amnesia	skos:exactMatch	DOID:11037	dissociative amnesia	semapv:ManualMappingCuration	2024-04-21
MONDO:0001187	urinary bladder cancer	skos:exactMatch	DOID:11054	urinary bladder cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001188	esophagus lymphoma	skos:exactMatch	DOID:1106	esophagus lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001192	esophageal melanoma	skos:exactMatch	DOID:1108	esophagus melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001197	qualitative platelet defect	skos:exactMatch	DOID:11125	qualitative platelet defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0001198	acquired thrombocytopenia	skos:exactMatch	DOID:11126	acquired thrombocytopenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001204	esophagus sarcoma	skos:exactMatch	DOID:1114	esophagus sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001212	non-suppurative otitis media	skos:exactMatch	DOID:11180	non-suppurative otitis media	semapv:ManualMappingCuration	2023-03-17
MONDO:0001214	acute conjunctivitis	skos:exactMatch	DOID:11184	acute conjunctivitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001222	congenital T-cell immunodeficiency	skos:exactMatch	DOID:11200	T cell deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0001227	chronic tympanitis	skos:exactMatch	DOID:11217	chronic tympanitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001229	small intestine diverticulitis	skos:exactMatch	DOID:11223	small intestine diverticulitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001230	acute orbital inflammation	skos:exactMatch	DOID:11230	acute orbital inflammation	semapv:ManualMappingCuration	2023-03-17
MONDO:0001235	appendix cancer	skos:exactMatch	DOID:11239	appendix cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001237	appendix lymphoma	skos:exactMatch	DOID:11241	appendix lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001240	neonatal anemia	skos:exactMatch	DOID:11244	neonatal anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001245	microcytic anemia	skos:exactMatch	DOID:11252	microcytic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001251	chronic apical periodontitis	skos:exactMatch	DOID:11269	chronic apical periodontitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001256	arteriovenous hemangioma/malformation	skos:exactMatch	DOID:11294	arteriovenous malformation	semapv:ManualMappingCuration	2023-03-17
MONDO:0001259	pituitary gland infarction	skos:exactMatch	DOID:1130	pituitary infarct	semapv:ManualMappingCuration	2023-03-17
MONDO:0001269	scleral disorder	skos:exactMatch	DOID:11343	scleral disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001275	spinal meningioma	skos:exactMatch	DOID:1138	spinal meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001277	cerebral arteritis	skos:exactMatch	DOID:11390	cerebral arteritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001279	intraspinal meningioma	skos:exactMatch	DOID:1140	spinal canal and spinal cord meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001280	choroiditis	skos:exactMatch	DOID:11406	choroiditis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001282	fallopian tube endometriosis	skos:exactMatch	DOID:11424	fallopian tube endometriosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001284	endometriosis of intestine	skos:exactMatch	DOID:11428	endometriosis of intestine	semapv:ManualMappingCuration	2024-04-21
MONDO:0001285	endometriosis of pelvic peritoneum	skos:exactMatch	DOID:11429	endometriosis of pelvic peritoneum	semapv:ManualMappingCuration	2023-03-17
MONDO:0001288	endometriosis of rectovaginal septum and vagina	skos:exactMatch	DOID:11431	endometriosis of rectovaginal septum and vagina	semapv:ManualMappingCuration	2023-03-17
MONDO:0001290	allergic cutaneous vasculitis	skos:exactMatch	DOID:11450	allergic cutaneous vasculitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001291	brain compression	skos:exactMatch	DOID:11457	brain compression	semapv:ManualMappingCuration	2023-03-17
MONDO:0001294	Horner syndrome	skos:exactMatch	DOID:11486	Horner's syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001296	acquired night blindness	skos:exactMatch	DOID:11491	acquired night blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0001298	congenital mitral valve insufficiency	skos:exactMatch	DOID:11502	mitral valve insufficiency	semapv:ManualMappingCuration	2024-04-21
MONDO:0001299	diabetic autonomic neuropathy	skos:exactMatch	DOID:11503	diabetic autonomic neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001300	autonomic neuropathy	skos:exactMatch	DOID:0060054	autonomic peripheral neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001300	autonomic neuropathy	skos:exactMatch	DOID:11504	autonomic neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001302	hypertensive heart disease	skos:exactMatch	DOID:11516	hypertensive heart disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001308	corneal deposit	skos:exactMatch	DOID:11547	corneal deposit	semapv:ManualMappingCuration	2023-03-17
MONDO:0001309	oculomotor nerve paralysis	skos:exactMatch	DOID:11550	oculomotor nerve paralysis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001314	chondrocalcinosis	skos:exactMatch	DOID:1156	chondrocalcinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001316	streptococcal meningitis	skos:exactMatch	DOID:11574	streptococcal meningitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001318	functional gastric disease	skos:exactMatch	DOID:1159	functional gastric disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001322	pericardium cancer	skos:exactMatch	DOID:116	pericardium cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001325	penile cancer	skos:exactMatch	DOID:11615	penile cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001328	thyroid hormone resistance syndrome	skos:exactMatch	DOID:11633	thyroid hormone resistance syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001330	presbyopia	skos:exactMatch	DOID:11638	presbyopia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001331	conjunctival deposit	skos:exactMatch	DOID:11653	conjunctival deposit	semapv:ManualMappingCuration	2023-03-17
MONDO:0001332	palindromic rheumatism	skos:exactMatch	DOID:1166	palindromic rheumatism	semapv:ManualMappingCuration	2023-03-17
MONDO:0001334	hypertrichosis of eyelid	skos:exactMatch	DOID:11669	hypertrichosis of eyelid	semapv:ManualMappingCuration	2023-03-17
MONDO:0001335	hypotrichosis of eyelid	skos:exactMatch	DOID:11671	hypotrichosis of eyelid	semapv:ManualMappingCuration	2024-04-21
MONDO:0001336	familial hyperlipidemia	skos:exactMatch	DOID:1168	familial hyperlipidemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001340	heart cancer	skos:exactMatch	DOID:117	heart cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001342	dysgammaglobulinemia	skos:exactMatch	DOID:11702	dysgammaglobulinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001347	facioscapulohumeral muscular dystrophy	skos:exactMatch	DOID:11727	facioscapulohumeral muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001350	parametrium malignant neoplasm	skos:exactMatch	DOID:11746	parametrium malignant neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0001351	uterine adnexa cancer	skos:exactMatch	DOID:11747	uterine adnexa cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0001355	ocular siderosis	skos:exactMatch	DOID:11754	siderosis of eye	semapv:ManualMappingCuration	2024-04-21
MONDO:0001357	hypochromic anemia	skos:exactMatch	DOID:11759	hypochromic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001369	chronic laryngitis	skos:exactMatch	DOID:11797	chronic laryngitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001370	pericardial effusion	skos:exactMatch	DOID:118	pericardial effusion	semapv:ManualMappingCuration	2023-03-17
MONDO:0001374	bladder sarcoma	skos:exactMatch	DOID:11812	bladder sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001377	vitreous syneresis	skos:exactMatch	DOID:11816	vitreous syneresis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001378	urachus cancer	skos:exactMatch	DOID:11817	urachus cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001381	bladder lymphoma	skos:exactMatch	DOID:11821	bladder lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001382	hepatorenal syndrome	skos:exactMatch	DOID:11823	hepatorenal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001387	penile sarcoma	skos:exactMatch	DOID:11838	penis sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001388	glans penis cancer	skos:exactMatch	DOID:11839	glans penis cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0001398	ureter benign neoplasm	skos:exactMatch	DOID:11885	ureteral benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0001399	ureter leiomyoma	skos:exactMatch	DOID:11887	ureter leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001400	schwannoma of ureter	skos:exactMatch	DOID:11888	schwannoma of ureter	semapv:ManualMappingCuration	2024-04-21
MONDO:0001402	vaginal cancer	skos:exactMatch	DOID:119	vaginal cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001407	tracheal cancer	skos:exactMatch	DOID:11920	tracheal cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001409	esophagitis	skos:exactMatch	DOID:11963	esophagitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001410	postmenopausal atrophic vaginitis	skos:exactMatch	DOID:11968	postmenopausal atrophic vaginitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001414	osteopoikilosis	skos:exactMatch	DOID:11991	Osteopoikilosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001417	tracheal lymphoma	skos:exactMatch	DOID:12001	tracheal lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001418	trachea sarcoma	skos:exactMatch	DOID:12002	trachea sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001420	trigeminal nerve neoplasm	skos:exactMatch	DOID:1201	trigeminal nerve neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0001421	frontal lobe neoplasm	skos:exactMatch	DOID:12016	frontal lobe neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0001422	primary aldosteronism	skos:exactMatch	DOID:12028	Conn's syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001423	drug-induced mental disorder	skos:exactMatch	DOID:1203	drug-induced mental disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001429	transient arthropathy	skos:exactMatch	DOID:12084	transient arthropathy	semapv:ManualMappingCuration	2024-04-21
MONDO:0001433	vaginal disorder	skos:exactMatch	DOID:121	vaginal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001434	inflammatory spondylopathy	skos:exactMatch	DOID:12105	inflammatory spondylopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001436	hemosiderosis	skos:exactMatch	DOID:12119	hemosiderosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001437	pulmonary alveolar proteinosis	skos:exactMatch	DOID:12120	pulmonary alveolar proteinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001438	postinflammatory pulmonary fibrosis	skos:exactMatch	DOID:12123	postinflammatory pulmonary fibrosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001444	Chagas disease	skos:exactMatch	DOID:12140	Chagas disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001458	ulnar nerve lesion	skos:exactMatch	DOID:12168	ulnar nerve lesion	semapv:ManualMappingCuration	2023-03-17
MONDO:0001459	radial neuropathy	skos:exactMatch	DOID:12171	radial neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001464	sigmoid colon cancer	skos:exactMatch	DOID:12192	sigmoid colon cancer	semapv:ManualMappingCuration	2023-11-19
MONDO:0001468	synovial plica syndrome	skos:exactMatch	DOID:12225	Plica syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0001474	chronic salpingo-oophoritis	skos:exactMatch	DOID:12265	chronic salpingo-oophoritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001475	neutropenia	skos:exactMatch	DOID:1227	neutropenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001476	coloboma	skos:exactMatch	DOID:12270	coloboma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001487	intrahepatic bile duct cancer	skos:exactMatch	DOID:12298	intrahepatic gall duct cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001493	chronic pulmonary heart disease	skos:exactMatch	DOID:12326	chronic pulmonary heart disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001498	varicocele	skos:exactMatch	DOID:12337	varicocele	semapv:ManualMappingCuration	2023-03-17
MONDO:0001499	retroperitoneal lymphoma	skos:exactMatch	DOID:12339	retroperitoneal lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001501	retroperitoneal sarcoma	skos:exactMatch	DOID:12341	retroperitoneal sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001502	retroperitoneum carcinoma	skos:exactMatch	DOID:12342	retroperitoneum carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001506	prostatocystitis	skos:exactMatch	DOID:12355	prostatocystitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001507	viral labyrinthitis	skos:exactMatch	DOID:12357	viral labyrinthitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001515	corneal degeneration	skos:exactMatch	DOID:1237	corneal degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0001519	entropion	skos:exactMatch	DOID:12397	entropion	semapv:ManualMappingCuration	2023-03-17
MONDO:0001528	vulva cancer	skos:exactMatch	DOID:1245	vulva cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001530	secondary hyperparathyroidism of renal origin	skos:exactMatch	DOID:12465	secondary hyperparathyroidism of renal origin	semapv:ManualMappingCuration	2023-03-17
MONDO:0001536	vaginal leiomyoma	skos:exactMatch	DOID:125	vagina leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001538	retinal ischemia	skos:exactMatch	DOID:12510	retinal ischemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0001539	retinal perforation	skos:exactMatch	DOID:12514	retinal perforation	semapv:ManualMappingCuration	2023-03-17
MONDO:0001543	lesion of sciatic nerve	skos:exactMatch	DOID:12528	lesion of sciatic nerve	semapv:ManualMappingCuration	2023-03-17
MONDO:0001549	hemolytic-uremic syndrome	skos:exactMatch	DOID:12554	hemolytic-uremic syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001551	ulceration of vulva	skos:exactMatch	DOID:12566	ulceration of vulva	semapv:ManualMappingCuration	2023-03-17
MONDO:0001554	phacogenic glaucoma	skos:exactMatch	DOID:12571	phacogenic glaucoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001557	olecranon bursitis	skos:exactMatch	DOID:12581	olecranon bursitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001563	vestibulocochlear nerve disorder	skos:exactMatch	DOID:12657	vestibulocochlear nerve disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001566	hypercalcemia disease	skos:exactMatch	DOID:12678	hypercalcemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001567	nephrocalcinosis	skos:exactMatch	DOID:12679	nephrocalcinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001572	leiomyoma	skos:exactMatch	DOID:127	leiomyoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001574	capillary disorder	skos:exactMatch	DOID:1271	capillary disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001575	chronic gonococcal salpingitis	skos:exactMatch	DOID:12718	chronic gonococcal salpingitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001576	telangiectasis	skos:exactMatch	DOID:1272	telangiectasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001580	lacrimal duct cancer	skos:exactMatch	DOID:12756	lacrimal duct cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001583	diabetic polyneuropathy	skos:exactMatch	DOID:12785	diabetic polyneuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001586	mucopolysaccharidosis type 1	skos:exactMatch	DOID:12802	mucopolysaccharidosis I	semapv:ManualMappingCuration	2023-03-17
MONDO:0001592	prolapse of female genital organ	skos:exactMatch	DOID:1284	prolapse of female genital organ	semapv:ManualMappingCuration	2023-03-17
MONDO:0001597	submandibular gland disorder	skos:exactMatch	DOID:12897	submandibular gland disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001604	lagophthalmos	skos:exactMatch	DOID:12959	lagophthalmos	semapv:ManualMappingCuration	2023-03-17
MONDO:0001606	central nervous system leukemia	skos:exactMatch	DOID:12969	central nervous system leukemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0001615	epidemic keratoconjunctivitis	skos:exactMatch	DOID:13014	shipyard eye	semapv:ManualMappingCuration	2024-04-21
MONDO:0001618	balanoposthitis	skos:exactMatch	DOID:13031	balanoposthitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001624	acute sphenoidal sinusitis	skos:exactMatch	DOID:13046	acute sphenoidal sinusitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001627	dementia	skos:exactMatch	DOID:1307	dementia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001628	tinea unguium	skos:exactMatch	DOID:13074	tinea unguium	semapv:ManualMappingCuration	2024-04-21
MONDO:0001634	bladder leiomyoma	skos:exactMatch	DOID:13109	bladder leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001639	deficiency anemia	skos:exactMatch	DOID:13121	deficiency anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001640	gonococcal spondylitis	skos:exactMatch	DOID:13127	gonococcal spondylitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001641	severe pre-eclampsia	skos:exactMatch	DOID:13129	severe pre-eclampsia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001644	acute proliferative glomerulonephritis	skos:exactMatch	DOID:13138	acute proliferative glomerulonephritis	semapv:ManualMappingCuration	2023-11-19
MONDO:0001645	crescentic glomerulonephritis	skos:exactMatch	DOID:13139	crescentic glomerulonephritis	semapv:ManualMappingCuration	2023-11-19
MONDO:0001649	fungal esophagitis	skos:exactMatch	DOID:13147	fungal esophagitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001650	acute cystitis	skos:exactMatch	DOID:13148	acute cystitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001651	scrotum squamous cell carcinoma	skos:exactMatch	DOID:13159	scrotum squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001652	scrotum melanoma	skos:exactMatch	DOID:13160	scrotum melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001657	brain cancer	skos:exactMatch	DOID:1319	brain cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001658	nontoxic goiter	skos:exactMatch	DOID:13195	nontoxic goiter	semapv:ManualMappingCuration	2023-03-17
MONDO:0001672	bronchus cancer	skos:exactMatch	DOID:1325	bronchus cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001673	diarrheal disease	skos:exactMatch	DOID:13250	diarrhea	semapv:ManualMappingCuration	2023-03-17
MONDO:0001674	diverticulitis of colon	skos:exactMatch	DOID:13254	diverticulitis of colon	semapv:ManualMappingCuration	2023-03-17
MONDO:0001676	erythropoietic protoporphyria	skos:exactMatch	DOID:13270	erythropoietic protoporphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0001678	intestinal tuberculosis	skos:exactMatch	DOID:13282	intestinal tuberculosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001680	vaginal mullerian papilloma	skos:exactMatch	DOID:133	vaginal Mullerian papilloma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001684	exocrine pancreatic insufficiency	skos:exactMatch	DOID:13316	exocrine pancreatic insufficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0001697	reading disorder	skos:exactMatch	DOID:13365	reading disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0001699	tinea manuum	skos:exactMatch	DOID:13369	tinea manuum	semapv:ManualMappingCuration	2024-04-21
MONDO:0001700	megaloblastic anemia	skos:exactMatch	DOID:13382	megaloblastic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001701	gastrointestinal anthrax	skos:exactMatch	DOID:13386	gastrointestinal anthrax	semapv:ManualMappingCuration	2024-04-21
MONDO:0001703	color vision disorder	skos:exactMatch	DOID:13399	color blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0001704	vaginal glandular neoplasm	skos:exactMatch	DOID:134	vaginal glandular tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0001705	pure red-cell aplasia	skos:exactMatch	DOID:1340	pure red-cell aplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001706	cerebral sarcoidosis	skos:exactMatch	DOID:13403	neurosarcoidosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001707	cardiac sarcoidosis	skos:exactMatch	DOID:13405	cardiac sarcoidosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001709	hypercalcemic sarcoidosis	skos:exactMatch	DOID:13407	hypercalcemic sarcoidosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001713	inherited aplastic anemia	skos:exactMatch	DOID:1342	congenital hypoplastic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001718	scleritis	skos:exactMatch	DOID:13452	scleritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001719	gonococcal bursitis	skos:exactMatch	DOID:13453	gonococcal bursitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001720	gonococcal synovitis	skos:exactMatch	DOID:13454	gonococcal synovitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001721	urethral intrinsic sphincter deficiency	skos:exactMatch	DOID:13461	urethral intrinsic sphincter deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0001724	supraglottis cancer	skos:exactMatch	DOID:13476	supraglottis cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001730	urethral syndrome	skos:exactMatch	DOID:13498	urethral syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001734	tuberous sclerosis	skos:exactMatch	DOID:13515	tuberous sclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001740	cornea squamous cell carcinoma	skos:exactMatch	DOID:13538	cornea squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001743	paranasal sinus lymphoma	skos:exactMatch	DOID:1355	paranasal sinus lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001744	angle-closure glaucoma	skos:exactMatch	DOID:13550	angle-closure glaucoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001747	tibial collateral ligament bursitis	skos:exactMatch	DOID:13566	tibial collateral ligament bursitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001748	maxillary sinus carcinoma	skos:exactMatch	DOID:1357	maxillary sinus cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001749	cortical senile cataract	skos:exactMatch	DOID:13574	cortical senile cataract	semapv:ManualMappingCuration	2023-11-19
MONDO:0001750	non-renal secondary hyperparathyroidism	skos:exactMatch	DOID:13575	non-renal secondary hyperparathyroidism	semapv:ManualMappingCuration	2023-03-17
MONDO:0001751	cholestasis	skos:exactMatch	DOID:13580	cholestasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001758	paranasal sinus sarcoma	skos:exactMatch	DOID:1362	paranasal sinus sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001760	photokeratitis	skos:exactMatch	DOID:13626	photokeratitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001763	ethmoid sinus cancer	skos:exactMatch	DOID:1363	ethmoid sinus cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001764	ethmoidal sinus neoplasm	skos:exactMatch	DOID:1364	ethmoidal sinus benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0001770	gastrin secretion abnormality	skos:exactMatch	DOID:13656	gastrin secretion abnormality	semapv:ManualMappingCuration	2023-03-17
MONDO:0001776	prostate calculus	skos:exactMatch	DOID:13689	prostate calculus	semapv:ManualMappingCuration	2024-04-21
MONDO:0001777	acute gonococcal cystitis	skos:exactMatch	DOID:13690	acute gonococcal cystitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001779	vaginal squamous papilloma	skos:exactMatch	DOID:137	vaginal squamous papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001780	premature ejaculation	skos:exactMatch	DOID:13709	premature ejaculation	semapv:ManualMappingCuration	2023-03-17
MONDO:0001784	malignant renovascular hypertension	skos:exactMatch	DOID:13730	malignant renovascular hypertension	semapv:ManualMappingCuration	2023-03-17
MONDO:0001785	malignant secondary hypertension	skos:exactMatch	DOID:13731	malignant secondary hypertension	semapv:ManualMappingCuration	2023-03-17
MONDO:0001790	spinal cord lipoma	skos:exactMatch	DOID:13743	spinal cord lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001798	hypermobility syndrome	skos:exactMatch	DOID:13781	hypermobility syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001806	vaginal squamous tumor	skos:exactMatch	DOID:138	vaginal squamous tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0001812	parasitic eyelid infestation	skos:exactMatch	DOID:13823	parasitic eyelid infestation	semapv:ManualMappingCuration	2023-03-17
MONDO:0001815	extrapyramidal and movement disease	skos:exactMatch	DOID:13839	extrapyramidal and movement disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001816	scleroperikeratitis	skos:exactMatch	DOID:13861	scleroperikeratitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001817	acute closed-angle glaucoma	skos:exactMatch	DOID:13862	acute closed-angle glaucoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001822	hypolipoproteinemia	skos:exactMatch	DOID:1387	hypolipoproteinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001823	sick sinus syndrome	skos:exactMatch	DOID:13884	sick sinus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001828	acquired color blindness	skos:exactMatch	DOID:13912	acquired color blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0001829	lumbosacral plexus lesion	skos:exactMatch	DOID:13913	lumbosacral plexus lesion	semapv:ManualMappingCuration	2023-03-17
MONDO:0001832	bacterial esophagitis	skos:exactMatch	DOID:13921	bacterial esophagitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001834	visual pathway disorder	skos:exactMatch	DOID:1393	visual pathway disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001835	facial paralysis	skos:exactMatch	DOID:13934	facial paralysis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001836	amenorrhea	skos:exactMatch	DOID:13938	amenorrhea	semapv:ManualMappingCuration	2023-11-19
MONDO:0001837	acute gonococcal salpingitis	skos:exactMatch	DOID:13942	acute gonococcal salpingitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001838	acute gonococcal prostatitis	skos:exactMatch	DOID:13943	acute gonococcal prostatitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001841	uterine corpus epithelioid leiomyoma	skos:exactMatch	DOID:13951	uterine corpus epithelioid leiomyoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001847	nuclear senile cataract	skos:exactMatch	DOID:13963	nuclear senile cataract	semapv:ManualMappingCuration	2023-03-17
MONDO:0001852	small intestine lymphoma	skos:exactMatch	DOID:13996	small intestine lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0001858	Tietze syndrome	skos:exactMatch	DOID:14021	Tietze's syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0001859	algoneurodystrophy	skos:exactMatch	DOID:14022	algoneurodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001876	renal artery atheroma	skos:exactMatch	DOID:14092	renal artery atheroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001878	acquired hypertrophic pyloric stenosis	skos:exactMatch	DOID:14099	acquired gastric outlet stenosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001879	anus cancer	skos:exactMatch	DOID:14110	anus cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0001884	abducens nerve neoplasm	skos:exactMatch	DOID:14125	abducens nerve neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0001888	anus lymphoma	skos:exactMatch	DOID:14139	anus lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001892	spinal cord lymphoma	skos:exactMatch	DOID:14150	spinal cord lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001893	spinal cord melanoma	skos:exactMatch	DOID:14151	spinal cord melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001894	spinal cord sarcoma	skos:exactMatch	DOID:14152	spinal cord sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001896	obstructive hydrocephalus	skos:exactMatch	DOID:14159	obstructive hydrocephalus	semapv:ManualMappingCuration	2023-03-17
MONDO:0001898	optic choroid disorder	skos:exactMatch	DOID:1417	choroid disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001902	congenital agammaglobulinemia	skos:exactMatch	DOID:14177	congenital hypogammaglobulinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0001903	calcific tendinitis	skos:exactMatch	DOID:14181	calcific tendinitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001907	adult dermatomyositis	skos:exactMatch	DOID:14202	adult dermatomyositis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001909	renal tubular acidosis	skos:exactMatch	DOID:14219	renal tubular acidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001917	chronic perichondritis of pinna	skos:exactMatch	DOID:14243	chronic perichondritis of pinna	semapv:ManualMappingCuration	2024-04-21
MONDO:0001920	chronic purulent otitis media	skos:exactMatch	DOID:14247	chronic purulent otitis media	semapv:ManualMappingCuration	2024-04-21
MONDO:0001926	ureteral disorder	skos:exactMatch	DOID:1426	ureteral disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001927	pulmonary valve insufficiency	skos:exactMatch	DOID:14265	pulmonary valve insufficiency	semapv:ManualMappingCuration	2024-06-23
MONDO:0001930	acute cholangitis	skos:exactMatch	DOID:14271	acute cholangitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0001933	endocrine pancreas disorder	skos:exactMatch	DOID:1428	endocrine pancreas disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0001938	vulvar dystrophy	skos:exactMatch	DOID:14292	vulvar dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0001941	blindness (disorder)	skos:exactMatch	DOID:1432	blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0001949	acute thyroiditis	skos:exactMatch	DOID:14353	acute thyroiditis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001955	protozoal dysentery	skos:exactMatch	DOID:14397	protozoal dysentery	semapv:ManualMappingCuration	2023-03-17
MONDO:0001966	chronic closed-angle glaucoma	skos:exactMatch	DOID:14445	chronic closed-angle glaucoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001967	gonadal dysgenesis	skos:exactMatch	DOID:14447	gonadal dysgenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001977	ureteral lymphoma	skos:exactMatch	DOID:14489	ureteral lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0001989	atrophic glossitis	skos:exactMatch	DOID:1453	atrophic glossitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0001991	malignant cardiac germ cell tumor	skos:exactMatch	DOID:14535	malignant cardiac germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0001999	primary pulmonary hypertension	skos:exactMatch	DOID:14557	primary pulmonary hypertension	semapv:ManualMappingCuration	2023-03-17
MONDO:0002000	anaerobic meningitis	skos:exactMatch	DOID:14559	anaerobic meningitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002004	atheroembolism of kidney	skos:exactMatch	DOID:1460	atheroembolism of kidney	semapv:ManualMappingCuration	2024-04-21
MONDO:0002009	major depressive disorder	skos:exactMatch	DOID:1470	major depressive disorder	semapv:ManualMappingCuration	2024-08-18
MONDO:0002012	methylmalonic acidemia	skos:exactMatch	DOID:14749	methylmalonic acidemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0002013	lymphangioma	skos:exactMatch	DOID:1475	lymphangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002014	autosomal recessive Ehlers-Danlos syndrome, vascular type	skos:exactMatch	DOID:14759	autosomal recessive type IV Ehlers-Danlos syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0002017	olivopontocerebellar atrophy	skos:exactMatch	DOID:14784	olivopontocerebellar atrophy	semapv:ManualMappingCuration	2023-11-19
MONDO:0002025	psychiatric disorder	skos:exactMatch	DOID:150	disease of mental health	semapv:ManualMappingCuration	2023-03-17
MONDO:0002026	candidiasis	skos:exactMatch	DOID:1508	candidiasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002028	personality disorder	skos:exactMatch	DOID:1510	personality disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002029	chronic gonorrhea of cervix	skos:exactMatch	DOID:1512	chronic gonorrhea of cervix	semapv:ManualMappingCuration	2024-04-21
MONDO:0002030	chronic cervicitis	skos:exactMatch	DOID:1513	chronic cervicitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002031	cecal disorder	skos:exactMatch	DOID:1518	cecal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002033	cecum cancer	skos:exactMatch	DOID:1521	cecum cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002034	cecum lymphoma	skos:exactMatch	DOID:1522	cecum lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002035	colon lymphoma	skos:exactMatch	DOID:1523	colon lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002036	penile disorder	skos:exactMatch	DOID:1529	penile disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002037	pleural disorder	skos:exactMatch	DOID:1532	pleural disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002038	head and neck carcinoma	skos:exactMatch	DOID:1542	head and neck carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002039	cognitive disorder	skos:exactMatch	DOID:1561	cognitive disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002040	dermatomycosis	skos:exactMatch	DOID:1563	dermatomycosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002041	fungal infectious disease	skos:exactMatch	DOID:1564	fungal infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002043	ectropion	skos:exactMatch	DOID:1570	ectropion	semapv:ManualMappingCuration	2023-03-17
MONDO:0002045	communicating hydrocephalus	skos:exactMatch	DOID:1573	communicating hydrocephalus	semapv:ManualMappingCuration	2023-03-17
MONDO:0002046	alcohol abuse	skos:exactMatch	DOID:1574	alcohol use disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002050	depressive disorder	skos:exactMatch	DOID:1596	depressive disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002052	lymphadenitis	skos:exactMatch	DOID:1602	lymphadenitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002057	breast leiomyoma	skos:exactMatch	DOID:1623	breast leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002058	breast adenoma	skos:exactMatch	DOID:1625	breast adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002060	intraductal papilloma	skos:exactMatch	DOID:1627	intraductal papilloma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002061	intraductal papillary breast neoplasm	skos:exactMatch	DOID:1628	intraductal papillary breast neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002070	ventricular septal defect	skos:exactMatch	DOID:1657	ventricular septal defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0002071	supratentorial cancer	skos:exactMatch	DOID:1659	supratentorial cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002073	malignant pineal area germ cell neoplasm	skos:exactMatch	DOID:1660	malignant pineal area germ cell neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002076	pneumothorax	skos:exactMatch	DOID:1673	pneumothorax	semapv:ManualMappingCuration	2023-03-17
MONDO:0002078	heart septal defect	skos:exactMatch	DOID:1681	heart septal defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0002083	Richter syndrome	skos:exactMatch	DOID:1703	Richter's syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0002087	peritoneum cancer	skos:exactMatch	DOID:1725	peritoneum cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002089	retinal vascular occlusion	skos:exactMatch	DOID:1729	retinal vascular occlusion	semapv:ManualMappingCuration	2023-03-17
MONDO:0002090	eccrine sweat gland neoplasm	skos:exactMatch	DOID:173	eccrine sweat gland neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002092	small intestine leiomyoma	skos:exactMatch	DOID:1738	small intestine leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002093	acanthoma	skos:exactMatch	DOID:174	acanthoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002095	vascular cancer	skos:exactMatch	DOID:175	vascular cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002100	cardiovascular cancer	skos:exactMatch	DOID:176	cardiovascular cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002101	facial nerve neoplasm	skos:exactMatch	DOID:1760	facial nerve neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002102	cheilitis	skos:exactMatch	DOID:1762	cheilitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002108	thyroid cancer	skos:exactMatch	DOID:1781	thyroid cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002112	benign peritoneal mesothelioma	skos:exactMatch	DOID:1789	benign peritoneal mesothelioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002113	peritoneal carcinoma	skos:exactMatch	DOID:1791	peritoneal carcinoma	semapv:ManualMappingCuration	2023-08-20
MONDO:0002114	pancreas lymphoma	skos:exactMatch	DOID:1792	pancreas lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002116	malignant exocrine pancreas neoplasm	skos:exactMatch	DOID:1795	malignant exocrine pancreas neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002117	pancreas sarcoma	skos:exactMatch	DOID:1796	pancreas sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002120	neuroendocrine carcinoma	skos:exactMatch	DOID:1800	neuroendocrine carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002122	neuritis	skos:exactMatch	DOID:1803	neuritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002123	calcinosis	skos:exactMatch	DOID:182	calcinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002132	skull cancer	skos:exactMatch	DOID:1863	skull cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002133	chronic rheumatic pericarditis	skos:exactMatch	DOID:1869	chronic rheumatic pericarditis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002134	physiological sexual disorder	skos:exactMatch	DOID:1876	sexual dysfunction	semapv:ManualMappingCuration	2023-03-17
MONDO:0002135	optic nerve disorder	skos:exactMatch	DOID:1891	optic nerve disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002137	noninfectious dermatoses of eyelid	skos:exactMatch	DOID:1894	noninfectious dermatoses of eyelid	semapv:ManualMappingCuration	2024-04-21
MONDO:0002138	allergic contact dermatitis of eyelid	skos:exactMatch	DOID:1895	allergic contact dermatitis of eyelid	semapv:ManualMappingCuration	2024-04-21
MONDO:0002140	vagina sarcoma	skos:exactMatch	DOID:1901	vagina sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002143	vaginal yolk sac tumor	skos:exactMatch	DOID:1910	vaginal yolk sac tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002145	disorder of sexual differentiation	skos:exactMatch	DOID:1923	disorder of sexual development	semapv:ManualMappingCuration	2023-03-17
MONDO:0002146	hypogonadism	skos:exactMatch	DOID:1924	hypogonadism	semapv:ManualMappingCuration	2023-03-17
MONDO:0002149	reproductive system cancer	skos:exactMatch	DOID:193	reproductive organ cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002150	hypothalamic disorder	skos:exactMatch	DOID:1931	hypothalamic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002158	fallopian tube cancer	skos:exactMatch	DOID:1964	fallopian tube cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002159	fallopian tube leiomyosarcoma	skos:exactMatch	DOID:1965	fallopian tube leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002162	fallopian tube adenosarcoma	skos:exactMatch	DOID:1973	fallopian tube adenosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002163	thymus lipoma	skos:exactMatch	DOID:1975	thymus lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002165	rectal neoplasm	skos:exactMatch	DOID:1984	rectal benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002166	rectum lymphoma	skos:exactMatch	DOID:1988	rectum lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002167	rectum malignant melanoma	skos:exactMatch	DOID:1992	rectum malignant melanoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002168	rectum sarcoma	skos:exactMatch	DOID:1995	rectum sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002170	chronic eustachian salpingitis	skos:exactMatch	DOID:1999	chronic eustachian salpingitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002171	giant cell tumor	skos:exactMatch	DOID:200	benign giant cell tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002172	otosalpingitis	skos:exactMatch	DOID:2000	otosalpingitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002175	degeneration of macula and posterior pole	skos:exactMatch	DOID:2007	degeneration of macula and posterior pole	semapv:ManualMappingCuration	2023-03-17
MONDO:0002177	hyperinsulinism	skos:exactMatch	DOID:2018	hyperinsulinism	semapv:ManualMappingCuration	2023-03-17
MONDO:0002178	placenta cancer	skos:exactMatch	DOID:2021	placenta cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002181	exostosis	skos:exactMatch	DOID:203	exostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002182	communication disorder	skos:exactMatch	DOID:2033	communication disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002185	hyperostosis	skos:exactMatch	DOID:205	hyperostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002186	acute maxillary sinusitis	skos:exactMatch	DOID:2050	acute maxillary sinusitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002187	vulvar disease	skos:exactMatch	DOID:2059	vulvar disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002190	vulvar syringoma	skos:exactMatch	DOID:2064	vulvar syringoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002191	syringoma	skos:exactMatch	DOID:2065	syringoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002192	vulvar angiokeratoma	skos:exactMatch	DOID:2066	vulvar angiokeratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002193	Bartholin gland benign neoplasm	skos:exactMatch	DOID:2068	Bartholin's gland benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002194	vestibular papilloma	skos:exactMatch	DOID:2071	vulvar squamous papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002195	vulvar squamous neoplasm	skos:exactMatch	DOID:2072	vulvar squamous tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002198	vulvar glandular neoplasm	skos:exactMatch	DOID:2076	vulvar glandular tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002201	vulvar trichoepithelioma	skos:exactMatch	DOID:2080	vulvar trichoepithelioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002203	constipation disorder	skos:exactMatch	DOID:2089	constipation	semapv:ManualMappingCuration	2023-03-17
MONDO:0002204	transient arthritis	skos:exactMatch	DOID:2092	transient arthritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002205	vulvar melanoma	skos:exactMatch	DOID:2093	vulvar melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002206	sweat gland cancer	skos:exactMatch	DOID:2095	sweat gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002207	vulval Paget disease	skos:exactMatch	DOID:2097	vulval Paget's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0002211	B cell deficiency	skos:exactMatch	DOID:2115	B cell deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0002214	brain germinoma	skos:exactMatch	DOID:2127	brain germinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002216	brain sarcoma	skos:exactMatch	DOID:2132	brain sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002217	central nervous system sarcoma	skos:exactMatch	DOID:2133	central nervous system sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002218	temporal lobe cancer	skos:exactMatch	DOID:2135	temporal lobe neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002220	tooth hard tissue disease	skos:exactMatch	DOID:214	teeth hard tissue disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002221	urethral urothelial papilloma	skos:exactMatch	DOID:2140	urethral urothelial papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002222	urethra leiomyoma	skos:exactMatch	DOID:2142	urethra leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002223	ovarian malignant mesothelioma	skos:exactMatch	DOID:2143	ovarian malignant mesothelioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002225	ovarian sarcoma	skos:exactMatch	DOID:2146	ovary sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002226	tuberculous oophoritis	skos:exactMatch	DOID:2148	tuberculous oophoritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002227	ovarian lymphoma	skos:exactMatch	DOID:2150	ovarian lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002229	ovarian epithelial tumor	skos:exactMatch	DOID:2152	ovary epithelial cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002230	ovarian Wilms tumor	skos:exactMatch	DOID:2153	ovarian Wilms' cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002232	nasal cavity disorder	skos:exactMatch	DOID:2163	nasal cavity disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002233	enamel caries	skos:exactMatch	DOID:217	enamel caries	semapv:ManualMappingCuration	2023-03-17
MONDO:0002234	vaginitis	skos:exactMatch	DOID:2170	vaginitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002236	ocular cancer	skos:exactMatch	DOID:2174	ocular cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002238	ascending colon cancer	skos:exactMatch	DOID:218	ascending colon cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002240	acute perichondritis of pinna	skos:exactMatch	DOID:221	acute perichondritis of pinna	semapv:ManualMappingCuration	2024-04-21
MONDO:0002243	hemorrhagic disease	skos:exactMatch	DOID:2213	hemorrhagic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002246	perichondritis of auricle	skos:exactMatch	DOID:222	perichondritis of auricle	semapv:ManualMappingCuration	2023-03-17
MONDO:0002249	thrombocytosis disease	skos:exactMatch	DOID:2228	thrombocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002253	spondylosis	skos:exactMatch	DOID:2247	spondylosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002254	syndromic disease	skos:exactMatch	DOID:225	syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0002256	cervix disorder	skos:exactMatch	DOID:2253	cervix disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002257	ankylosis	skos:exactMatch	DOID:227	ankylosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002258	pharyngitis	skos:exactMatch	DOID:2275	pharyngitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002259	gonadal disorder	skos:exactMatch	DOID:2277	gonadal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002260	hidradenitis	skos:exactMatch	DOID:2282	hidradenitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002262	capillary lymphangioma	skos:exactMatch	DOID:2286	capillary lymphangioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002265	stereotypic movement disorder	skos:exactMatch	DOID:2303	stereotypic movement disorder	semapv:ManualMappingCuration	2023-11-19
MONDO:0002266	malt worker's lung	skos:exactMatch	DOID:2314	malt worker's lung	semapv:ManualMappingCuration	2024-04-21
MONDO:0002270	viral gastritis	skos:exactMatch	DOID:2327	viral gastritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002273	plasma protein metabolism disease	skos:exactMatch	DOID:2345	plasma protein metabolism disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002277	arteriosclerosis disorder	skos:exactMatch	DOID:2348	arteriosclerotic cardiovascular disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002277	arteriosclerosis disorder	skos:exactMatch	DOID:2349	arteriosclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002278	benign colon neoplasm	skos:exactMatch	DOID:235	colonic benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002279	iron metabolism disease	skos:exactMatch	DOID:2351	iron metabolism disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002280	anemia	skos:exactMatch	DOID:2355	anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0002281	macrocytic anemia	skos:exactMatch	DOID:2361	macrocytic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0002282	West Nile fever	skos:exactMatch	DOID:2366	West Nile fever	semapv:ManualMappingCuration	2023-03-17
MONDO:0002283	neuroaxonal dystrophy	skos:exactMatch	DOID:2367	neuroaxonal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002286	renal artery disease	skos:exactMatch	DOID:2388	renal artery disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002289	iris disorder	skos:exactMatch	DOID:240	iris disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002291	cutaneous granular cell tumor	skos:exactMatch	DOID:2410	skin granular cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002295	skin glomus tumor	skos:exactMatch	DOID:2430	skin glomus tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002297	epidermal appendage tumor	skos:exactMatch	DOID:2433	epidermal appendage tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002300	dermis tumor	skos:exactMatch	DOID:2438	dermis tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002304	protein S deficiency	skos:exactMatch	DOID:2451	protein S deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0002307	blepharoconjunctivitis	skos:exactMatch	DOID:2456	blepharoconjunctivitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002311	retinal vascular disorder	skos:exactMatch	DOID:2462	retinal vascular disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002312	opportunistic mycosis	skos:exactMatch	DOID:2473	opportunistic mycosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002314	chronic conjunctivitis	skos:exactMatch	DOID:2475	chronic conjunctivitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002316	motor peripheral neuropathy	skos:exactMatch	DOID:2477	motor peripheral neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002317	central nervous system origin vertigo	skos:exactMatch	DOID:2479	central nervous system origin vertigo	semapv:ManualMappingCuration	2023-03-17
MONDO:0002318	trachea leiomyoma	skos:exactMatch	DOID:248	trachea leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002319	phosphorus metabolism disease	skos:exactMatch	DOID:2485	phosphorus metabolism disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002320	congenital nervous system disorder	skos:exactMatch	DOID:2490	congenital nervous system abnormality	semapv:ManualMappingCuration	2023-03-17
MONDO:0002321	sensory peripheral neuropathy	skos:exactMatch	DOID:2491	sensory peripheral neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002326	alcohol-induced mental disorder	skos:exactMatch	DOID:251	alcohol-induced mental disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002328	intracranial hemangioma	skos:exactMatch	DOID:2517	intracranial structure hemangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002331	nephrosis	skos:exactMatch	DOID:2527	nephrosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002333	splenic abscess	skos:exactMatch	DOID:2530	splenic abscess	semapv:ManualMappingCuration	2024-04-21
MONDO:0002334	hematopoietic and lymphoid system neoplasm	skos:exactMatch	DOID:2531	hematologic cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002337	intra-abdominal hemangioma	skos:exactMatch	DOID:254	hemangioma of intra-abdominal structure	semapv:ManualMappingCuration	2023-03-17
MONDO:0002341	granulomatous angiitis	skos:exactMatch	DOID:2555	granulomatous angiitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002342	chondromalacia	skos:exactMatch	DOID:2557	chondromalacia	semapv:ManualMappingCuration	2023-03-17
MONDO:0002343	splenic hemangioma	skos:exactMatch	DOID:256	hemangioma of spleen	semapv:ManualMappingCuration	2024-04-21
MONDO:0002345	cervicitis	skos:exactMatch	DOID:2568	cervicitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002350	familial nephrotic syndrome	skos:exactMatch	DOID:2590	familial nephrotic syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0002351	glottis cancer	skos:exactMatch	DOID:2595	glottis cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002353	glottis neoplasm	skos:exactMatch	DOID:2597	glottis neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002354	benign laryngeal neoplasm	skos:exactMatch	DOID:2598	laryngeal benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002355	glottis carcinoma	skos:exactMatch	DOID:2599	glottis carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002358	laryngeal carcinoma	skos:exactMatch	DOID:2600	laryngeal carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002359	periosteal chondroma	skos:exactMatch	DOID:2601	juxtacortical chondroma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002360	chondroma	skos:exactMatch	DOID:2602	chondroma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002363	papilloma	skos:exactMatch	DOID:2615	papilloma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002365	kidney hemangiopericytoma	skos:exactMatch	DOID:262	kidney hemangiopericytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002366	autonomic nervous system neoplasm	skos:exactMatch	DOID:2621	autonomic nervous system neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002367	kidney cancer	skos:exactMatch	DOID:263	kidney cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002368	papillary serous cystadenocarcinoma	skos:exactMatch	DOID:2632	papillary serous adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002369	cystadenoma	skos:exactMatch	DOID:2634	cystadenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002372	ovarian monodermal and highly specialized teratoma	skos:exactMatch	DOID:2641	ovarian germ cell monodermal and highly specialized teratoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002373	benign mesothelioma	skos:exactMatch	DOID:2645	benign mesothelioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002375	sebaceous adenoma	skos:exactMatch	DOID:2648	sebaceous adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002376	spleen angiosarcoma	skos:exactMatch	DOID:265	spleen angiosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002379	cystic teratoma	skos:exactMatch	DOID:2660	cystic teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002380	myoepithelial tumor	skos:exactMatch	DOID:2661	myoepithelioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002387	liver angiosarcoma	skos:exactMatch	DOID:268	liver angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002395	renal adenoma	skos:exactMatch	DOID:2697	renal adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002397	liver sarcoma	skos:exactMatch	DOID:270	liver sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002398	mucinous adenofibroma	skos:exactMatch	DOID:2700	mucinous adenofibroma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002401	malignant tenosynovial giant cell tumor	skos:exactMatch	DOID:2704	malignant giant cell tumor of the tendon sheath	semapv:ManualMappingCuration	2024-04-21
MONDO:0002402	malignant giant cell tumor	skos:exactMatch	DOID:2705	malignant giant cell tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002403	synovium cancer	skos:exactMatch	DOID:2706	synovium cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002404	liver hemangioma	skos:exactMatch	DOID:271	hemangioma of liver	semapv:ManualMappingCuration	2023-03-17
MONDO:0002405	hepatic vascular disorder	skos:exactMatch	DOID:272	hepatic vascular disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002406	dermatitis	skos:exactMatch	DOID:2723	dermatitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002407	capillary hemangioma	skos:exactMatch	DOID:2725	capillary hemangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002408	hereditary hyperbilirubinemia	skos:exactMatch	DOID:2741	bilirubin metabolic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002412	disorder of glycogen metabolism	skos:exactMatch	DOID:0050728	glycogen metabolism disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002412	disorder of glycogen metabolism	skos:exactMatch	DOID:2747	glycogen storage disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002413	glycogen storage disease I	skos:exactMatch	DOID:0081329	glycogen storage disease I	semapv:ManualMappingCuration	2023-05-21
MONDO:0002414	gastric hemangioma	skos:exactMatch	DOID:275	gastric hemangioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002415	bone carcinoma	skos:exactMatch	DOID:2762	bone carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002416	ethmoid sinus squamous cell carcinoma	skos:exactMatch	DOID:2763	ethmoid sinus squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002418	ethmoid sinus adenocarcinoma	skos:exactMatch	DOID:2766	ethmoid sinus adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002419	transient tic disorder	skos:exactMatch	DOID:2768	transient tic disorder	semapv:ManualMappingCuration	2024-04-21
MONDO:0002420	tic disorder	skos:exactMatch	DOID:2769	tic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002422	adamantinoma	skos:exactMatch	DOID:2775	long bone adamantinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002422	adamantinoma	skos:exactMatch	DOID:2776	adamantinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002423	rectosigmoid junction neoplasm	skos:exactMatch	DOID:2780	rectosigmoid junction neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002424	rectosigmoid carcinoma	skos:exactMatch	DOID:2781	rectosigmoid cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002425	rectosigmoid junction cancer	skos:exactMatch	DOID:2782	rectosigmoid junction cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002426	lung sarcoma	skos:exactMatch	DOID:2784	lung sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002427	cerebellar disorder	skos:exactMatch	DOID:2786	cerebellar disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002428	protozoa infectious disease	skos:exactMatch	DOID:2789	parasitic protozoa infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002429	idiopathic interstitial pneumonia	skos:exactMatch	DOID:2797	idiopathic interstitial pneumonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0002432	malignant neoplasm of acoustic nerve	skos:exactMatch	DOID:2814	malignant neoplasm of acoustic nerve	semapv:ManualMappingCuration	2024-04-21
MONDO:0002434	oculomotor nerve cancer	skos:exactMatch	DOID:2816	malignant oculomotor nerve tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002435	oculomotor nerve neoplasm	skos:exactMatch	DOID:2817	cranial nerve III tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002436	nasal disorder	skos:exactMatch	DOID:2825	nose disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002438	acquired polycythemia	skos:exactMatch	DOID:2834	acquired polycythemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0002441	Jervell and Lange-Nielsen syndrome	skos:exactMatch	DOID:2842	Jervell-Lange Nielsen syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0002443	bruxism	skos:exactMatch	DOID:2846	bruxism	semapv:ManualMappingCuration	2023-11-19
MONDO:0002448	laryngeal sarcoma	skos:exactMatch	DOID:2877	larynx sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002450	prostatic adenoma	skos:exactMatch	DOID:2883	prostatic adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002451	benign prostate phyllodes tumor	skos:exactMatch	DOID:2885	benign prostate phyllodes tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002452	prostate leiomyoma	skos:exactMatch	DOID:2887	prostate leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002453	retrocochlear disease	skos:exactMatch	DOID:2889	retrocochlear disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002457	Treacher-Collins syndrome	skos:exactMatch	DOID:2908	Treacher Collins syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0002459	type IV hypersensitivity disease	skos:exactMatch	DOID:2916	hypersensitivity reaction type IV disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002460	lacrimal system cancer	skos:exactMatch	DOID:292	lacrimal system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002462	glomerulonephritis	skos:exactMatch	DOID:2921	glomerulonephritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002463	lacrimal gland carcinoma	skos:exactMatch	DOID:293	lacrimal gland carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002464	lacrimal gland cancer	skos:exactMatch	DOID:294	lacrimal gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002465	bronchiolitis	skos:exactMatch	DOID:2942	bronchiolitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002466	eye carcinoma	skos:exactMatch	DOID:295	eye carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002468	hyperimmunoglobulin syndrome	skos:exactMatch	DOID:2959	hyperimmunoglobulin syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0002469	lacrimal gland carcinoma ex pleomorphic adenoma	skos:exactMatch	DOID:296	mixed lacrimal gland cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002470	photosensitive trichothiodystrophy	skos:exactMatch	DOID:2960	photosensitive trichothiodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002471	bursitis	skos:exactMatch	DOID:2965	bursitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002474	primary hyperoxaluria	skos:exactMatch	DOID:2977	primary hyperoxaluria	semapv:ManualMappingCuration	2023-03-17
MONDO:0002475	lacrimal gland adenocarcinoma	skos:exactMatch	DOID:298	lacrimal gland adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002477	prostate neuroendocrine neoplasm	skos:exactMatch	DOID:2992	prostate neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002478	mixed germ cell-sex cord-stromal tumor	skos:exactMatch	DOID:2996	mixed germ cell-sex cord neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002480	endometrioid tumor	skos:exactMatch	DOID:3001	female reproductive endometrioid cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002481	ovarian neuroendocrine neoplasm	skos:exactMatch	DOID:3002	ovary neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002482	nipple neoplasm	skos:exactMatch	DOID:3003	nipple benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002483	breast myoepithelial tumor	skos:exactMatch	DOID:3004	breast myoepithelial neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002485	breast neuroendocrine neoplasm	skos:exactMatch	DOID:3009	breast neuroendocrine neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002486	lobular neoplasia	skos:exactMatch	DOID:3010	lobular neoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0002487	breast granular cell tumor	skos:exactMatch	DOID:3011	breast granular cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002488	intraductal breast neoplasm	skos:exactMatch	DOID:3013	intraductal breast benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002490	breast sarcoma	skos:exactMatch	DOID:3017	breast sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002491	substance abuse	skos:exactMatch	DOID:302	substance abuse	semapv:ManualMappingCuration	2023-03-17
MONDO:0002492	acute kidney failure	skos:exactMatch	DOID:3021	acute kidney failure	semapv:ManualMappingCuration	2023-03-17
MONDO:0002493	prostatic acinar adenocarcinoma	skos:exactMatch	DOID:3024	prostatic acinar adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002494	substance-related disorder	skos:exactMatch	DOID:303	substance-related disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002495	colon signet ring cell adenocarcinoma	skos:exactMatch	DOID:3033	colon signet ring adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002503	adult astrocytic tumor	skos:exactMatch	DOID:3076	adult astrocytic tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002505	childhood astrocytic tumor	skos:exactMatch	DOID:3079	childhood astrocytic tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002507	gingival overgrowth	skos:exactMatch	DOID:3086	gingival overgrowth	semapv:ManualMappingCuration	2023-03-17
MONDO:0002508	gingivitis	skos:exactMatch	DOID:3087	gingivitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002512	papillary adenocarcinoma	skos:exactMatch	DOID:3112	papillary adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002513	kidney benign neoplasm	skos:exactMatch	DOID:3116	kidney benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002516	digestive system cancer	skos:exactMatch	DOID:3119	gastrointestinal system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002518	gallbladder papillary neoplasm	skos:exactMatch	DOID:3120	gallbladder papillomatosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002520	hepatic porphyria	skos:exactMatch	DOID:3133	acute porphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0002523	cutaneous mucinosis	skos:exactMatch	DOID:3141	mucinoses	semapv:ManualMappingCuration	2023-03-17
MONDO:0002525	inherited lipid metabolism disorder	skos:exactMatch	DOID:3146	lipid metabolism disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0002527	keratoacanthoma	skos:exactMatch	DOID:3149	keratoacanthoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002528	synovium neoplasm	skos:exactMatch	DOID:315	synovium neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002529	skin squamous cell carcinoma	skos:exactMatch	DOID:3151	skin squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002532	squamous cell neoplasm	skos:exactMatch	DOID:3168	squamous cell neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002533	papillary adenoma	skos:exactMatch	DOID:3172	papillary adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002534	fallopian tube papilloma	skos:exactMatch	DOID:3173	fallopian tube serous papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002536	skin papilloma	skos:exactMatch	DOID:3178	skin papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002537	inverted papilloma	skos:exactMatch	DOID:3179	inverted papilloma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002540	childhood oligodendroglioma	skos:exactMatch	DOID:3183	childhood oligodendroglioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002541	spinal cord oligodendroglioma	skos:exactMatch	DOID:3184	spinal cord oligodendroglioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002542	spinal cord glioma	skos:exactMatch	DOID:3185	spinal cord glioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002543	adult oligodendroglioma	skos:exactMatch	DOID:3186	adult oligodendroglioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002544	brain oligodendroglioma	skos:exactMatch	DOID:3187	brain oligodendroglioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002547	nerve sheath neoplasm	skos:exactMatch	DOID:3193	peripheral nerve sheath neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002548	cellular schwannoma	skos:exactMatch	DOID:3196	cellular schwannoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002555	trigeminal schwannoma	skos:exactMatch	DOID:3202	neurilemmoma of the fifth cranial nerve	semapv:ManualMappingCuration	2024-04-21
MONDO:0002558	melanotic neurilemmoma	skos:exactMatch	DOID:3205	melanotic neurilemmoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002561	lysosomal storage disease	skos:exactMatch	DOID:3211	lysosomal storage disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002562	demyelinating disease	skos:exactMatch	DOID:3213	demyelinating disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002564	jejunal neoplasm	skos:exactMatch	DOID:3218	jejunal neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002567	tracheal disorder	skos:exactMatch	DOID:3225	tracheal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002574	prostate embryonal rhabdomyosarcoma	skos:exactMatch	DOID:3251	prostate embryonal rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002576	embryonal extrahepatic bile duct rhabdomyosarcoma	skos:exactMatch	DOID:3253	embryonal extrahepatic bile duct rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002577	extrahepatic bile duct rhabdomyosarcoma	skos:exactMatch	DOID:3254	bile duct rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002579	orbit embryonal rhabdomyosarcoma	skos:exactMatch	DOID:3258	orbit embryonal rhabdomyosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002580	orbit rhabdomyosarcoma	skos:exactMatch	DOID:3259	orbit rhabdomyosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002581	spindle cell rhabdomyosarcoma	skos:exactMatch	DOID:3260	spindle cell rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002583	mucinous ovarian cystadenoma	skos:exactMatch	DOID:3267	mucinous ovarian cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002586	thymus cancer	skos:exactMatch	DOID:3277	thymus cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002588	thymoma type A	skos:exactMatch	DOID:3279	spindle cell thymoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002592	invasive malignant thymoma	skos:exactMatch	DOID:3283	invasive malignant thymoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002597	notochordal tumor	skos:exactMatch	DOID:3303	notochordal cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002598	germinoma	skos:exactMatch	DOID:3304	germinoma	semapv:ManualMappingCuration	2023-08-20
MONDO:0002601	teratoma	skos:exactMatch	DOID:3307	teratoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002603	angiomyolipoma	skos:exactMatch	DOID:3314	angiomyolipoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002604	pericytic neoplasm	skos:exactMatch	DOID:3316	perivascular tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002605	hepatic angiomyolipoma	skos:exactMatch	DOID:3317	hepatic angiomyolipoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002606	epithelioid type angiomyolipoma	skos:exactMatch	DOID:3318	epithelioid type angiomyolipoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002610	purpura	skos:exactMatch	DOID:3326	purpura	semapv:ManualMappingCuration	2023-03-17
MONDO:0002612	frontal lobe epilepsy	skos:exactMatch	DOID:3331	frontal lobe epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002614	bone inflammation disease	skos:exactMatch	DOID:3342	bone inflammation disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002615	xanthomatosis	skos:exactMatch	DOID:3345	xanthomatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002616	mesenchymal cell neoplasm	skos:exactMatch	DOID:3350	mesenchymal cell neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002617	bone angiosarcoma	skos:exactMatch	DOID:3351	bone angioendothelial sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002618	undifferentiated high grade pleomorphic sarcoma of bone	skos:exactMatch	DOID:3352	malignant fibrous histiocytoma of bone	semapv:ManualMappingCuration	2023-03-17
MONDO:0002619	bone fibrosarcoma	skos:exactMatch	DOID:3354	fibrosarcoma of bone	semapv:ManualMappingCuration	2023-03-17
MONDO:0002621	extraosseous osteosarcoma	skos:exactMatch	DOID:3357	extraosseous osteosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002623	pediatric osteosarcoma	skos:exactMatch	DOID:3361	childhood osteosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002624	bone leiomyosarcoma	skos:exactMatch	DOID:3367	bone leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002625	Ewing sarcoma of bone	skos:exactMatch	DOID:3368	Ewing sarcoma of bone	semapv:ManualMappingCuration	2024-04-21
MONDO:0002627	chondroblastic osteosarcoma	skos:exactMatch	DOID:3372	chondroblastic osteosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002628	peripheral osteosarcoma	skos:exactMatch	DOID:3374	peripheral osteosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002629	bone osteosarcoma	skos:exactMatch	DOID:3376	bone osteosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002630	small cell osteogenic sarcoma	skos:exactMatch	DOID:3377	small cell osteogenic sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002631	conventional osteosarcoma	skos:exactMatch	DOID:3378	conventional central osteosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002631	conventional osteosarcoma	skos:exactMatch	DOID:7602	conventional osteosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002633	cranial nerve neoplasm	skos:exactMatch	DOID:338	cranial nerve neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002634	liposarcoma of bone	skos:exactMatch	DOID:3381	liposarcoma of bone	semapv:ManualMappingCuration	2024-04-21
MONDO:0002635	periodontal disorder	skos:exactMatch	DOID:3388	periodontal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002642	trochlear nerve neoplasm	skos:exactMatch	DOID:3421	trochlear nerve neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002645	cerebritis	skos:exactMatch	DOID:3431	cerebritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002646	viral laryngitis	skos:exactMatch	DOID:3436	viral laryngitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002647	laryngitis	skos:exactMatch	DOID:3437	laryngitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002648	mammary Paget disease	skos:exactMatch	DOID:3443	mammary Paget's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0002649	scrotum Paget disease	skos:exactMatch	DOID:3444	scrotum Paget's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0002650	scrotal carcinoma	skos:exactMatch	DOID:3445	scrotal carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002651	anal Paget disease	skos:exactMatch	DOID:3446	anal Paget's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0002652	anus adenocarcinoma	skos:exactMatch	DOID:3447	anus adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002653	Paget disease of the penis	skos:exactMatch	DOID:3448	penis Paget's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0002654	uterine disorder	skos:exactMatch	DOID:345	uterine disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002655	cutaneous Paget disease	skos:exactMatch	DOID:3450	cutaneous Paget's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0002661	uveal disorder	skos:exactMatch	DOID:3480	uveal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002664	extrahepatic bile duct signet ring cell carcinoma	skos:exactMatch	DOID:3494	bile duct signet ring cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002665	extrahepatic bile duct adenocarcinoma	skos:exactMatch	DOID:3495	extrahepatic bile duct adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002666	pancreatic signet ring cell adenocarcinoma	skos:exactMatch	DOID:3497	pancreatic signet ring cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002667	gallbladder signet ring cell adenocarcinoma	skos:exactMatch	DOID:3499	gallbladder signet ring cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002671	signet ring cell breast carcinoma	skos:exactMatch	DOID:3503	breast signet ring cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002672	acinar prostate adenocarcinoma, signet ring variant	skos:exactMatch	DOID:3504	prostate signet ring cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002674	stricture or kinking of ureter	skos:exactMatch	DOID:3508	stricture or kinking of ureter	semapv:ManualMappingCuration	2023-03-17
MONDO:0002676	adult fibrosarcoma	skos:exactMatch	DOID:3516	adult fibrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002677	conventional fibrosarcoma	skos:exactMatch	DOID:3517	conventional fibrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002678	pediatric fibrosarcoma	skos:exactMatch	DOID:3520	childhood fibrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002679	cerebral infarction	skos:exactMatch	DOID:3526	cerebral infarction	semapv:ManualMappingCuration	2023-03-17
MONDO:0002683	adult choroid plexus neoplasm	skos:exactMatch	DOID:3542	adult choroid plexus cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002684	atypical choroid plexus papilloma	skos:exactMatch	DOID:3544	atypical choroid plexus papilloma	semapv:ManualMappingCuration	2023-08-20
MONDO:0002685	childhood choroid plexus carcinoma	skos:exactMatch	DOID:3545	childhood choroid plexus cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002691	liver cancer	skos:exactMatch	DOID:3571	liver cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002697	ovarian gonadoblastoma	skos:exactMatch	DOID:3578	ovarian gonadoblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002698	testicular gonadoblastoma	skos:exactMatch	DOID:3579	testicular gonadoblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002703	appendix mucinous cystadenocarcinoma	skos:exactMatch	DOID:3607	appendix mucinous cystadenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002705	breast mucinous cystadenocarcinoma	skos:exactMatch	DOID:3609	breast mucinous cystadenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002706	cervix endometriosis	skos:exactMatch	DOID:361	cervix endometriosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002708	retinitis	skos:exactMatch	DOID:3612	retinitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002710	infiltrating angiolipoma	skos:exactMatch	DOID:3615	infiltrating angiolipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002715	uterine cancer	skos:exactMatch	DOID:363	uterine cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002716	childhood spinal cord tumor	skos:exactMatch	DOID:3637	childhood spinal cord tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002718	central nervous system teratoma	skos:exactMatch	DOID:3640	central nervous system teratoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002720	sella turcica neoplasm	skos:exactMatch	DOID:3643	sella turcica neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002721	necrosis of pituitary	skos:exactMatch	DOID:3646	necrosis of pituitary	semapv:ManualMappingCuration	2023-03-17
MONDO:0002722	olfactory nerve neoplasm	skos:exactMatch	DOID:8256	olfactory neural tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002727	olfactory nerve disorder	skos:exactMatch	DOID:367	olfactory nerve disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002730	childhood kidney neoplasm	skos:exactMatch	DOID:3675	childhood kidney cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002731	cerebral hemisphere cancer	skos:exactMatch	DOID:368	cerebrum cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002732	lung benign neoplasm	skos:exactMatch	DOID:3683	lung benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002734	anal mucinous adenocarcinoma	skos:exactMatch	DOID:3691	anal colloid adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002735	anal canal adenocarcinoma	skos:exactMatch	DOID:3692	anal canal adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002736	ampulla of vater mucinous adenocarcinoma	skos:exactMatch	DOID:3693	ampulla of Vater mucinous adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002738	acute transudative otitis media	skos:exactMatch	DOID:3697	acute transudative otitis media	semapv:ManualMappingCuration	2024-04-21
MONDO:0002739	extrahepatic bile duct mucinous adenocarcinoma	skos:exactMatch	DOID:3698	bile duct mucinous adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002740	uterine ligament mucinous adenocarcinoma	skos:exactMatch	DOID:3699	uterine ligament mucinous adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002741	uterine ligament adenocarcinoma	skos:exactMatch	DOID:3700	uterine ligament adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002742	cervical mucinous adenocarcinoma	skos:exactMatch	DOID:3701	cervical mucinous adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002744	fallopian tube mucinous adenocarcinoma	skos:exactMatch	DOID:3704	fallopian tube mucinous adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002745	fallopian tube mucinous tumor	skos:exactMatch	DOID:3705	fallopian tube mucinous tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002746	fallopian tube adenocarcinoma	skos:exactMatch	DOID:3706	fallopian tube adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002748	rectum mucinous adenocarcinoma	skos:exactMatch	DOID:3709	rectum mucinous adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002749	extracranial neuroblastoma	skos:exactMatch	DOID:371	extracranial neuroblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002758	vulva verrucous carcinoma	skos:exactMatch	DOID:3740	vulva verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002759	bladder verrucous carcinoma	skos:exactMatch	DOID:3741	bladder verrucous squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002761	cervical verrucous carcinoma	skos:exactMatch	DOID:3743	cervical verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002762	esophagus verrucous carcinoma	skos:exactMatch	DOID:3747	esophagus verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002763	urethral verrucous carcinoma	skos:exactMatch	DOID:3749	urethral verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002764	urethra squamous cell carcinoma	skos:exactMatch	DOID:3750	urethra squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002765	plantar verrucous skin carcinoma	skos:exactMatch	DOID:3751	plantar verrucous skin carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002766	larynx verrucous carcinoma	skos:exactMatch	DOID:3752	larynx verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002772	intraventricular meningioma	skos:exactMatch	DOID:3772	intraventricular meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002775	anovulation	skos:exactMatch	DOID:3781	anovulation	semapv:ManualMappingCuration	2023-03-17
MONDO:0002779	central nervous system chondroma	skos:exactMatch	DOID:3813	central nervous system chondroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002785	skull base neoplasm	skos:exactMatch	DOID:3842	skull base cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002786	diencephalic cancer	skos:exactMatch	DOID:3843	diencephalic neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002794	adult medulloblastoma	skos:exactMatch	DOID:3864	adult medulloblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002795	adult central nervous system primitive neuroectodermal neoplasm	skos:exactMatch	DOID:3865	adult central nervous system embryonal tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0002797	childhood medulloblastoma	skos:exactMatch	DOID:3869	childhood medulloblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002798	childhood central nervous system primitive neuroectodermal neoplasm	skos:exactMatch	DOID:3870	childhood central nervous system embryonal tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002805	hidradenoma	skos:exactMatch	DOID:3896	hidradenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002808	pancreatic serous cystadenoma	skos:exactMatch	DOID:3917	pancreatic serous cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002809	pancreatic cystadenoma	skos:exactMatch	DOID:3918	pancreatic cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002810	pancreatic serous cystic neoplasm	skos:exactMatch	DOID:3919	pancreatic serous cystic neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002814	adrenal carcinoma	skos:exactMatch	DOID:3950	adrenal carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002815	acute myocarditis	skos:exactMatch	DOID:3951	acute myocarditis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002816	adrenal cortex disorder	skos:exactMatch	DOID:3952	adrenal cortex disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002817	adrenal gland cancer	skos:exactMatch	DOID:3953	adrenal gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002822	trabecular adenocarcinoma	skos:exactMatch	DOID:3965	Merkel cell carcinoma	semapv:ManualMappingCuration	2023-11-19
MONDO:0002824	extrinsic cardiomyopathy	skos:exactMatch	DOID:3978	extrinsic cardiomyopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002828	Bartholin gland transitional cell carcinoma	skos:exactMatch	DOID:3998	Bartholin's gland transitional cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002833	fallopian tube transitional cell carcinoma	skos:exactMatch	DOID:4008	fallopian tube transitional cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002834	primary prostate urothelial carcinoma	skos:exactMatch	DOID:4011	prostate transitional cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002836	urethra transitional cell carcinoma	skos:exactMatch	DOID:4013	urethra transitional cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002837	sarcomatoid transitional cell carcinoma	skos:exactMatch	DOID:4014	sarcomatoid transitional cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002842	bacterial gastritis	skos:exactMatch	DOID:4033	bacterial gastritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002843	fungal gastritis	skos:exactMatch	DOID:4034	fungal gastritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002847	skeletal muscle cancer	skos:exactMatch	DOID:4043	skeletal muscle cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002848	skeletal muscle neoplasm	skos:exactMatch	DOID:4044	skeletal muscle neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0002849	liver rhabdomyosarcoma	skos:exactMatch	DOID:4047	liver rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002850	central nervous system rhabdomyosarcoma	skos:exactMatch	DOID:4048	central nervous system rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002851	mediastinum rhabdomyosarcoma	skos:exactMatch	DOID:4049	mediastinum rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002852	mediastinum sarcoma	skos:exactMatch	DOID:4050	mediastinum sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002853	rectum rhabdomyosarcoma	skos:exactMatch	DOID:4053	rectum rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002854	prostate sarcoma	skos:exactMatch	DOID:4054	prostate sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002855	ectomesenchymoma	skos:exactMatch	DOID:4055	ectomesenchymoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002856	gallbladder rhabdomyosarcoma	skos:exactMatch	DOID:4057	gallbladder rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002857	gallbladder sarcoma	skos:exactMatch	DOID:4058	gallbladder sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002858	ovary rhabdomyosarcoma	skos:exactMatch	DOID:4059	ovary rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002859	breast rhabdomyosarcoma	skos:exactMatch	DOID:4060	breast rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002860	testis rhabdomyosarcoma	skos:exactMatch	DOID:4061	testis rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002861	testis sarcoma	skos:exactMatch	DOID:4062	testis sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002862	bile duct sarcoma	skos:exactMatch	DOID:4064	bile duct sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002863	rhabdomyosarcoma with mixed embryonal and alveolar features	skos:exactMatch	DOID:4065	mixed type rhabdomyosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002864	anus rhabdomyosarcoma	skos:exactMatch	DOID:4066	anus rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002865	anus sarcoma	skos:exactMatch	DOID:4067	anus sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002866	duodenal disorder	skos:exactMatch	DOID:4072	duodenum disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002867	pancreatic cystadenocarcinoma	skos:exactMatch	DOID:4073	pancreatic cystadenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002870	tricuspid valve insufficiency	skos:exactMatch	DOID:4080	tricuspid valve insufficiency	semapv:ManualMappingCuration	2024-04-21
MONDO:0002871	testicular trophoblastic tumor	skos:exactMatch	DOID:4084	testicular trophoblastic tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002872	trophoblastic neoplasm	skos:exactMatch	DOID:4085	trophoblastic neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002874	testicular pure germ cell tumor	skos:exactMatch	DOID:4087	testicular pure germ cell tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002875	parasitic ectoparasitic infectious disease	skos:exactMatch	DOID:4110	parasitic ectoparasitic infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002876	cervical adenosarcoma	skos:exactMatch	DOID:4111	cervical adenosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002877	cervical carcinosarcoma	skos:exactMatch	DOID:4112	cervical carcinosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002878	uterine corpus adenosarcoma	skos:exactMatch	DOID:4113	uterine corpus adenosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002879	uterine body mixed cancer	skos:exactMatch	DOID:4114	uterine body mixed cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002880	ovarian adenosarcoma	skos:exactMatch	DOID:4115	ovarian mesodermal adenosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002881	vaginal adenosarcoma	skos:exactMatch	DOID:4117	vaginal adenosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002882	colon neuroendocrine neoplasm	skos:exactMatch	DOID:4118	colon neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002883	intestinal neuroendocrine neoplasm	skos:exactMatch	DOID:4119	intestinal neuroendocrine benign tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0002884	nail disorder	skos:exactMatch	DOID:4123	nail disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002886	common bile duct disorder	skos:exactMatch	DOID:4137	common bile duct disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002887	bile duct disorder	skos:exactMatch	DOID:4138	bile duct disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002898	skin cancer	skos:exactMatch	DOID:4159	skin cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002900	cerebral neuroblastoma	skos:exactMatch	DOID:0080905	central nervous system neuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002900	cerebral neuroblastoma	skos:exactMatch	DOID:4164	cerebral neuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002901	blood group incompatibility	skos:exactMatch	DOID:4176	blood group incompatibility	semapv:ManualMappingCuration	2023-03-17
MONDO:0002907	intracranial thrombosis	skos:exactMatch	DOID:4193	intracranial thrombosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002912	brainstem cancer	skos:exactMatch	DOID:4203	brain stem cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002913	cerebellar neoplasm	skos:exactMatch	DOID:4205	cerebellum cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002914	childhood brain stem neoplasm	skos:exactMatch	DOID:4206	childhood brain stem neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002915	childhood infratentorial neoplasm	skos:exactMatch	DOID:4207	childhood infratentorial neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0002917	disorder of pilosebaceous unit	skos:exactMatch	DOID:421	hair disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002921	congenital structural myopathy	skos:exactMatch	DOID:422	congenital structural myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002923	uterine corpus endometrial stromal sarcoma	skos:exactMatch	DOID:4227	uterine corpus endometrial stromal sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002924	smooth muscle cancer	skos:exactMatch	DOID:4230	smooth muscle cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002927	spindle cell sarcoma	skos:exactMatch	DOID:4235	spindle cell sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002928	carcinosarcoma	skos:exactMatch	DOID:4236	carcinosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002930	kidney sarcoma	skos:exactMatch	DOID:4242	kidney sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002933	osteosclerosis	skos:exactMatch	DOID:4254	osteosclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0002935	penis basal cell carcinoma	skos:exactMatch	DOID:4277	penis basal cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002936	scrotum basal cell carcinoma	skos:exactMatch	DOID:4278	scrotum basal cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002943	external ear basal cell carcinoma	skos:exactMatch	DOID:4287	external ear basal cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002944	external ear carcinoma	skos:exactMatch	DOID:4288	external ear carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002951	skin adenoid basal cell carcinoma	skos:exactMatch	DOID:4294	adenoid basal cell carcinoma	semapv:ManualMappingCuration	2024-02-18
MONDO:0002955	vulva basal cell carcinoma	skos:exactMatch	DOID:4301	vulva basal cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002959	radiculopathy	skos:exactMatch	DOID:4306	radiculopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0002962	epidermolytic acanthoma	skos:exactMatch	DOID:4323	epidermolytic acanthoma	semapv:ManualMappingCuration	2023-11-19
MONDO:0002966	splenic manifestation of prolymphocytic leukemia	skos:exactMatch	DOID:4334	splenic manifestation of prolymphocytic leukemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0002967	dermatophytosis of scalp or beard	skos:exactMatch	DOID:4337	tinea capitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0002969	ciliary body cancer	skos:exactMatch	DOID:4352	ciliary body cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0002970	ciliary body disorder	skos:exactMatch	DOID:4353	ciliary body disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0002973	epithelioid cell melanoma	skos:exactMatch	DOID:4360	epithelioid cell melanoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002974	cervical cancer	skos:exactMatch	DOID:4362	cervical cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0002975	malignant breast melanoma	skos:exactMatch	DOID:4364	malignant breast melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002977	autoimmune disorder of the nervous system	skos:exactMatch	DOID:438	autoimmune disease of the nervous system	semapv:ManualMappingCuration	2023-03-17
MONDO:0002979	papillary squamous carcinoma	skos:exactMatch	DOID:4385	papillary squamous carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002981	peripheral primitive neuroectodermal tumor of bone	skos:exactMatch	DOID:4388	bone peripheral neuroepithelioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0002989	benign fibrous histiocytoma	skos:exactMatch	DOID:4415	fibrous histiocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002996	cavernous sinus meningioma	skos:exactMatch	DOID:4435	cavernous sinus meningioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002998	skull base meningioma	skos:exactMatch	DOID:4437	skull base meningioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0002999	central nervous system germinoma	skos:exactMatch	DOID:4438	central nervous system germinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003000	central nervous system germ cell tumor	skos:exactMatch	DOID:4439	central nervous system germ cell tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003001	seminoma	skos:exactMatch	DOID:4440	seminoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003002	dysgerminoma	skos:exactMatch	DOID:4441	dysgerminoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003003	cervical alveolar soft part sarcoma	skos:exactMatch	DOID:4442	cervical alveolar soft part sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003005	macular retinal edema	skos:exactMatch	DOID:4449	macular retinal edema	semapv:ManualMappingCuration	2023-03-17
MONDO:0003007	childhood kidney cell carcinoma	skos:exactMatch	DOID:4454	childhood kidney cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003008	hereditary renal cell carcinoma	skos:exactMatch	DOID:4455	hereditary renal cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003017	malignant peritoneal solitary fibrous tumor	skos:exactMatch	DOID:4490	malignant peritoneal solitary fibrous tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003019	potassium deficiency disease	skos:exactMatch	DOID:4500	hypokalemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0003021	central nervous system angiosarcoma	skos:exactMatch	DOID:4504	central nervous system angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003022	pediatric angiosarcoma	skos:exactMatch	DOID:4505	childhood angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003023	aorta angiosarcoma	skos:exactMatch	DOID:4510	aorta angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003024	breast angiosarcoma	skos:exactMatch	DOID:4511	breast angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003026	gallbladder angiosarcoma	skos:exactMatch	DOID:4513	gallbladder angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003027	thyroid gland angiosarcoma	skos:exactMatch	DOID:4514	thyroid angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003028	thyroid sarcoma	skos:exactMatch	DOID:4515	thyroid sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003029	skin angiosarcoma	skos:exactMatch	DOID:4517	skin angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003030	endometrioid stromal sarcoma of the cervix	skos:exactMatch	DOID:4520	cervical endometrial stromal sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003031	endometrioid stromal and related neoplasms of the cervix	skos:exactMatch	DOID:4521	cervix endometrial stromal tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003033	prostate angiosarcoma	skos:exactMatch	DOID:4524	prostate angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003034	mediastinum angiosarcoma	skos:exactMatch	DOID:4525	mediastinum angiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003035	ovarian angiosarcoma	skos:exactMatch	DOID:4527	ovarian angiosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003036	mucoepidermoid carcinoma	skos:exactMatch	DOID:4531	mucoepidermoid carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003037	hypotrichosis	skos:exactMatch	DOID:4535	hypotrichosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003041	pediatric mesenchymal chondrosarcoma	skos:exactMatch	DOID:4546	childhood mesenchymal chondrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003042	adult mesenchymal chondrosarcoma	skos:exactMatch	DOID:4547	adult mesenchymal chondrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003047	thymic large cell neuroendocrine carcinoma	skos:exactMatch	DOID:4553	thymus large cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003049	ovarian large-cell neuroendocrine carcinoma	skos:exactMatch	DOID:4555	ovarian large-cell neuroendocrine carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003053	choroid plexus meningioma	skos:exactMatch	DOID:4584	choroid plexus meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003054	benign meningioma	skos:exactMatch	DOID:4587	benign meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003057	pediatric meningioma	skos:exactMatch	DOID:4593	childhood meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003059	bile duct cancer	skos:exactMatch	DOID:4606	bile duct cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003060	biliary tract cancer	skos:exactMatch	DOID:4607	biliary tract cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003061	benign muscle neoplasm	skos:exactMatch	DOID:2691	myoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003061	benign muscle neoplasm	skos:exactMatch	DOID:461	muscle benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003064	inverted transitional cell papilloma	skos:exactMatch	DOID:4630	inverted transitional papilloma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003066	submandibular adenitis	skos:exactMatch	DOID:4636	submandibular adenitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003067	cervical lymphadenitis	skos:exactMatch	DOID:4637	cervical adenitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003073	trilateral retinoblastoma	skos:exactMatch	DOID:4647	trilateral retinoblastoma	semapv:ManualMappingCuration	2023-11-19
MONDO:0003076	unilateral retinoblastoma	skos:exactMatch	DOID:4651	unilateral retinoblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003081	thalamic disorder	skos:exactMatch	DOID:4662	thalamic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003086	thymic mucoepidermoid carcinoma	skos:exactMatch	DOID:4678	thymus mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003087	mucoepidermoid breast carcinoma	skos:exactMatch	DOID:4679	breast mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003089	extrahepatic bile duct mucoepidermoid carcinoma	skos:exactMatch	DOID:4681	bile duct mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003090	extrahepatic bile duct carcinoma	skos:exactMatch	DOID:4682	extrahepatic bile duct carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003091	cutaneous mucoepidermoid carcinoma	skos:exactMatch	DOID:4683	cutaneous mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003092	lacrimal gland mucoepidermoid carcinoma	skos:exactMatch	DOID:4685	lacrimal gland mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003093	mucoepidermoid esophageal carcinoma	skos:exactMatch	DOID:4686	mucoepidermoid esophageal carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003095	laryngeal mucoepidermoid carcinoma	skos:exactMatch	DOID:4688	laryngeal mucoepidermoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003097	childhood mediastinal neurogenic neoplasm	skos:exactMatch	DOID:4690	childhood mediastinal neurogenic tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003098	mediastinal neural neoplasm	skos:exactMatch	DOID:4691	malignant mediastinal neurogenic neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003100	nerve plexus neoplasm	skos:exactMatch	DOID:4693	nerve plexus neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003103	nerve root neoplasm	skos:exactMatch	DOID:4698	nerve root neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003104	epicardium cancer	skos:exactMatch	DOID:4699	epicardium cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0003107	infratentorial cancer	skos:exactMatch	DOID:4706	infratentorial cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003110	skin hemangioma	skos:exactMatch	DOID:471	skin hemangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003111	gastric neuroendocrine neoplasm	skos:exactMatch	DOID:4715	gastric neuroendocrine neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003112	malignant gastric germ cell tumor	skos:exactMatch	DOID:4716	malignant gastric germ cell tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003113	extragonadal germ cell cancer	skos:exactMatch	DOID:4717	extragonadal germ cell cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003120	mixed testicular germ cell cancer	skos:exactMatch	DOID:4743	mixed testicular germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003122	striatonigral degeneration	skos:exactMatch	DOID:4751	striatonigral degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0003124	testicular Leydig cell tumor	skos:exactMatch	DOID:4756	testicular Leydig cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003125	testicular sex cord-stromal neoplasm	skos:exactMatch	DOID:4757	testicular sex cord-stromal neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003126	breast hemangioma	skos:exactMatch	DOID:476	breast hemangioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003134	proliferative glomerulonephritis	skos:exactMatch	DOID:4778	proliferative glomerulonephritis	semapv:ManualMappingCuration	2023-11-19
MONDO:0003142	intracranial primitive neuroectodermal tumor	skos:exactMatch	DOID:4788	intracranial primitive neuroectodermal tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003143	angiokeratoma	skos:exactMatch	DOID:479	angiokeratoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003145	supratentorial primitive neuroectodermal tumor	skos:exactMatch	DOID:4791	supratentorial primitive neuroectodermal tumor	semapv:ManualMappingCuration	2023-11-19
MONDO:0003153	adult brainstem glioma	skos:exactMatch	DOID:4813	adult brain stem glioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003154	hemangioma of peripheral nerve	skos:exactMatch	DOID:482	hemangioma of peripheral nerve	semapv:ManualMappingCuration	2024-04-21
MONDO:0003157	disappearing bone disease	skos:exactMatch	DOID:4837	Gorham's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003158	malignant myoepithelioma	skos:exactMatch	DOID:4838	myoepithelial carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003159	vascular hemostatic disease	skos:exactMatch	DOID:484	vascular hemostatic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003164	cauda equina neoplasm	skos:exactMatch	DOID:4847	cauda equina neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003165	cerebellar astrocytoma	skos:exactMatch	DOID:4848	cerebellar astrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003168	cerebellar pilocytic astrocytoma	skos:exactMatch	DOID:4853	pilocytic astrocytoma of cerebellum	semapv:ManualMappingCuration	2023-03-17
MONDO:0003169	diencephalic astrocytomas	skos:exactMatch	DOID:4855	diencephalic astrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003171	pineal gland astrocytoma	skos:exactMatch	DOID:4858	pineal gland astrocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003173	brain stem astrocytic neoplasm	skos:exactMatch	DOID:4860	brain stem astrocytic neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003175	salivary gland adenoid cystic carcinoma	skos:exactMatch	DOID:4866	salivary gland adenoid cystic carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003177	prostate adenoid cystic carcinoma	skos:exactMatch	DOID:4868	prostate adenoid cystic carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003180	cutaneous adenocystic carcinoma	skos:exactMatch	DOID:4871	cutaneous adenocystic carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003181	lung adenoid cystic carcinoma	skos:exactMatch	DOID:4872	lung adenoid cystic carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003182	anterior horn disorder	skos:exactMatch	DOID:4873	anterior horn cell disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003186	esophageal adenoid cystic carcinoma	skos:exactMatch	DOID:4878	esophageal adenoid cystic carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003187	Bartholin gland adenoid cystic carcinoma	skos:exactMatch	DOID:4879	Bartholin's gland adenoid cystic carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003189	middle ear adenocarcinoma	skos:exactMatch	DOID:4892	middle ear adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003190	middle ear carcinoma	skos:exactMatch	DOID:4893	middle ear carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003193	bile duct adenocarcinoma	skos:exactMatch	DOID:4896	bile duct adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003194	hemangioma of lung	skos:exactMatch	DOID:490	hemangioma of lung	semapv:ManualMappingCuration	2023-03-17
MONDO:0003195	peritoneal serous adenocarcinoma	skos:exactMatch	DOID:4901	peritoneal serous adenocarcinoma	semapv:ManualMappingCuration	2023-08-20
MONDO:0003196	appendix carcinoma	skos:exactMatch	DOID:4902	appendix carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003197	granular cell carcinoma	skos:exactMatch	DOID:4903	granular cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003199	anal carcinoma	skos:exactMatch	DOID:4908	anal carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003200	urethra adenocarcinoma	skos:exactMatch	DOID:4910	urethra adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003204	villous adenocarcinoma	skos:exactMatch	DOID:4917	villous adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003205	renal pelvis adenocarcinoma	skos:exactMatch	DOID:4918	renal pelvis adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003206	acquired hemangioma	skos:exactMatch	DOID:492	acquired hemangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003209	thymus gland adenocarcinoma	skos:exactMatch	DOID:4923	thymus adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003211	nasal cavity adenocarcinoma	skos:exactMatch	DOID:4930	nasal cavity adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003212	nasal cavity carcinoma	skos:exactMatch	DOID:4931	nasal cavity carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003214	apocrine adenocarcinoma	skos:exactMatch	DOID:4933	apocrine carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003215	apocrine sweat gland cancer	skos:exactMatch	DOID:4934	apocrine sweat gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003216	ureter adenocarcinoma	skos:exactMatch	DOID:4938	ureter adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003218	adenocarcinoma in situ	skos:exactMatch	DOID:4943	adenocarcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0003219	gastroesophageal junction adenocarcinoma	skos:exactMatch	DOID:4944	gastroesophageal junction adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003222	central nervous system melanocytic neoplasm	skos:exactMatch	DOID:4955	central nervous system melanocytic neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003223	meninges hemangiopericytoma	skos:exactMatch	DOID:4957	meninges hemangiopericytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003225	bone marrow disorder	skos:exactMatch	DOID:4961	bone marrow disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003234	optic nerve astrocytoma	skos:exactMatch	DOID:4991	optic nerve astrocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003236	atypical polypoid adenomyoma	skos:exactMatch	DOID:4993	atypical polypoid adenomyoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003237	adenomyoma of uterine corpus	skos:exactMatch	DOID:4994	adenomyoma of uterine corpus	semapv:ManualMappingCuration	2023-03-17
MONDO:0003241	central nervous system hemangioma	skos:exactMatch	DOID:501	central nervous system hemangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003243	hepatocellular clear cell carcinoma	skos:exactMatch	DOID:5016	hepatocellular clear cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003244	central nervous system mesenchymal non-meningothelial tumor	skos:exactMatch	DOID:502	central nervous system mesenchymal non-meningothelial tumor	semapv:ManualMappingCuration	2023-09-24
MONDO:0003248	adult pineal parenchymal tumor	skos:exactMatch	DOID:5031	adult pineal parenchymal tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003249	pineal gland cancer	skos:exactMatch	DOID:5032	pineal gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003250	benign granular cell tumor	skos:exactMatch	DOID:5039	myoblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003251	esophageal granular cell tumor	skos:exactMatch	DOID:5040	malignant granular cell esophageal tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003252	granular cell cancer	skos:exactMatch	DOID:5042	malignant granular cell myoblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003253	vulvar granular cell tumor	skos:exactMatch	DOID:5043	vulvar granular cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003254	cardiac granular cell neoplasm	skos:exactMatch	DOID:5044	cardiac granular cell neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003255	mediastinal granular cell myoblastoma	skos:exactMatch	DOID:5046	mediastinal granular cell myoblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003257	posterior pituitary gland neoplasm	skos:exactMatch	DOID:5048	posterior pituitary gland neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003260	adult cerebellar neoplasm	skos:exactMatch	DOID:5056	adult cerebellar neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003263	childhood cerebellar neoplasm	skos:exactMatch	DOID:5059	childhood cerebellar neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003265	adjustment disorder	skos:exactMatch	DOID:507	adjustment disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0003268	mixed glioma	skos:exactMatch	DOID:5076	mixed glioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003274	thoracic cancer	skos:exactMatch	DOID:5093	thoracic cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003275	middle ear cancer	skos:exactMatch	DOID:5099	middle ear cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003276	middle ear disorder	skos:exactMatch	DOID:5100	middle ear disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003277	malignant ear neoplasm	skos:exactMatch	DOID:5101	ear cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003278	inner ear cancer	skos:exactMatch	DOID:5102	inner ear cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0003281	ovarian cystic teratoma	skos:exactMatch	DOID:5118	ovarian cystic teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003284	mediastinum leiomyoma	skos:exactMatch	DOID:5123	mediastinum leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003285	fallopian tube leiomyoma	skos:exactMatch	DOID:5124	fallopian tube leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003286	extrahepatic bile duct leiomyoma	skos:exactMatch	DOID:5125	extrahepatic bile duct leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003287	central nervous system leiomyoma	skos:exactMatch	DOID:5126	central nervous system leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003291	leiomyoma cutis	skos:exactMatch	DOID:5132	leiomyoma cutis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003292	anus leiomyoma	skos:exactMatch	DOID:5134	anus leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003293	lung leiomyoma	skos:exactMatch	DOID:5136	lung leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003294	pericardium leiomyoma	skos:exactMatch	DOID:5137	pericardium leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003295	leiomyomatosis	skos:exactMatch	DOID:5138	leiomyomatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003297	gallbladder leiomyoma	skos:exactMatch	DOID:5140	gallbladder leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003298	vulvar leiomyoma	skos:exactMatch	DOID:5142	vulvar leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003299	colorectal leiomyoma	skos:exactMatch	DOID:5143	large bowel leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003300	appendix leiomyoma	skos:exactMatch	DOID:5146	appendix leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003312	ovarian endometrioid stromal and related neoplasms	skos:exactMatch	DOID:5169	ovarian endometrioid stromal sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003313	endometrioid stromal sarcoma of the vagina	skos:exactMatch	DOID:5170	vaginal endometrial stromal sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003314	endometrioid stromal and related neoplasms of the vagina	skos:exactMatch	DOID:5171	vaginal endometrial stromal tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003315	endometrium carcinoma in situ	skos:exactMatch	DOID:5172	endometrium carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0003319	scrotum neoplasm	skos:exactMatch	DOID:518	scrotum neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003321	hereditary Wilms tumor	skos:exactMatch	DOID:5183	hereditary Wilms' tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003327	peripheral ganglioneuroblastoma	skos:exactMatch	DOID:5195	peripheral nervous system ganglioneuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003331	ovarian monodermal teratoma	skos:exactMatch	DOID:5207	monodermal teratoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003332	malignant struma ovarii	skos:exactMatch	DOID:5208	malignant struma ovarii	semapv:ManualMappingCuration	2024-04-21
MONDO:0003333	benign struma ovarii	skos:exactMatch	DOID:5209	benign struma ovarii	semapv:ManualMappingCuration	2024-04-21
MONDO:0003334	demyelinating polyneuropathy	skos:exactMatch	DOID:5214	demyelinating polyneuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0003335	chronic polyneuropathy	skos:exactMatch	DOID:5221	chronic polyneuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0003337	acute hemorrhagic encephalitis	skos:exactMatch	DOID:5224	acute hemorrhagic encephalitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003340	malignant glomus tumor	skos:exactMatch	DOID:5233	glomangiosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003342	benign perivascular tumor	skos:exactMatch	DOID:5238	benign perivascular tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003343	retinal hemangioblastoma	skos:exactMatch	DOID:5240	retinal hemangioblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003346	central nervous system vasculitis	skos:exactMatch	DOID:525	central nervous system vasculitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003349	central nervous system leiomyosarcoma	skos:exactMatch	DOID:5254	central nervous system leiomyosarcoma	semapv:ManualMappingCuration	2023-09-24
MONDO:0003350	granular cell leiomyosarcoma	skos:exactMatch	DOID:5258	granular cell leiomyosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003351	colon leiomyosarcoma	skos:exactMatch	DOID:5259	colon leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003352	colon sarcoma	skos:exactMatch	DOID:5260	colon sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003353	heart leiomyosarcoma	skos:exactMatch	DOID:5261	heart leiomyosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003354	heart sarcoma	skos:exactMatch	DOID:5262	heart sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003357	lung leiomyosarcoma	skos:exactMatch	DOID:5265	lung leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003358	anus leiomyosarcoma	skos:exactMatch	DOID:5267	anus leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003360	small intestine leiomyosarcoma	skos:exactMatch	DOID:5271	small intestine leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003361	small intestinal sarcoma	skos:exactMatch	DOID:5272	small intestinal sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003362	cutaneous leiomyosarcoma	skos:exactMatch	DOID:5273	cutaneous leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003363	malignant dermis tumor	skos:exactMatch	DOID:5274	malignant dermis tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003364	gallbladder leiomyosarcoma	skos:exactMatch	DOID:5275	gallbladder leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003365	esophagus leiomyosarcoma	skos:exactMatch	DOID:5276	esophagus leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003366	hydrarthrosis	skos:exactMatch	DOID:528	hydrarthrosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003367	gastric leiomyosarcoma	skos:exactMatch	DOID:5280	gastric leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003368	prostate leiomyosarcoma	skos:exactMatch	DOID:5282	prostate leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003369	vagina leiomyosarcoma	skos:exactMatch	DOID:5283	vagina leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003370	retroperitoneal leiomyosarcoma	skos:exactMatch	DOID:5284	retroperitoneal leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003371	breast leiomyosarcoma	skos:exactMatch	DOID:5285	breast leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003373	kidney leiomyosarcoma	skos:exactMatch	DOID:5287	kidney leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003374	laryngeal leiomyosarcoma	skos:exactMatch	DOID:5288	larynx leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003376	mediastinum leiomyosarcoma	skos:exactMatch	DOID:5292	mediastinum leiomyosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003377	extrahepatic bile duct leiomyosarcoma	skos:exactMatch	DOID:5293	extrahepatic bile duct leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003378	liver leiomyosarcoma	skos:exactMatch	DOID:5296	liver leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003379	rectum leiomyosarcoma	skos:exactMatch	DOID:5297	rectum leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003383	fallopian tube clear cell adenocarcinoma	skos:exactMatch	DOID:5301	fallopian tube clear cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003384	uterine ligament clear cell adenocarcinoma	skos:exactMatch	DOID:5302	uterine ligament clear cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003386	bladder clear cell adenocarcinoma	skos:exactMatch	DOID:5306	bladder clear cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003387	urethra clear cell adenocarcinoma	skos:exactMatch	DOID:5307	urethra clear cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003388	ampulla of vater clear cell adenocarcinoma	skos:exactMatch	DOID:5308	ampulla of Vater clear cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003391	vulvar alveolar soft part sarcoma	skos:exactMatch	DOID:5313	vulvar alveolar soft part sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003392	fallopian tube germ cell tumor	skos:exactMatch	DOID:5324	fallopian tube germ cell cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0003393	thymus gland disorder	skos:exactMatch	DOID:533	thymus gland disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003395	testicular granulosa cell tumor	skos:exactMatch	DOID:5331	testicular granulosa cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003396	epulis	skos:exactMatch	DOID:5337	epulis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003399	pineal region yolk sac tumor	skos:exactMatch	DOID:5341	pineal region yolk sac tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003400	childhood endodermal sinus tumor	skos:exactMatch	DOID:5342	childhood endodermal sinus tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003401	central nervous system endodermal sinus tumor	skos:exactMatch	DOID:5343	central nervous system endodermal sinus tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003403	testicular non-seminomatous germ cell cancer	skos:exactMatch	DOID:5345	testicular non-seminomatous germ cell cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003404	adult yolk sac tumor	skos:exactMatch	DOID:5348	adult endodermal sinus tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003405	adult central nervous system germ cell tumor	skos:exactMatch	DOID:5349	central nervous system adult germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003406	sleep-wake disorder	skos:exactMatch	DOID:535	sleep disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0003408	ovarian primitive germ cell tumor	skos:exactMatch	DOID:5351	ovarian primitive germ cell tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003409	colonic disorder	skos:exactMatch	DOID:5353	colonic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003410	Wolffian duct adenocarcinoma	skos:exactMatch	DOID:5368	Wolffian duct adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003411	breast hemangiopericytoma	skos:exactMatch	DOID:5370	breast hemangiopericytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003412	retroperitoneal hemangiopericytoma	skos:exactMatch	DOID:5373	retroperitoneal hemangiopericytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003413	hair follicle neoplasm	skos:exactMatch	DOID:5375	hair follicle neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003419	Bartholin gland adenoma	skos:exactMatch	DOID:5382	Bartholin's gland adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003420	bile duct cystadenoma	skos:exactMatch	DOID:5384	bile duct cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003422	lung adenoma	skos:exactMatch	DOID:5386	lung adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003423	middle ear adenoma	skos:exactMatch	DOID:5387	middle ear adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003425	ophthalmoplegia	skos:exactMatch	DOID:539	ophthalmoplegia	semapv:ManualMappingCuration	2023-11-19
MONDO:0003427	bronchus adenoma	skos:exactMatch	DOID:5391	bronchus adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003428	brain hemangioma	skos:exactMatch	DOID:5393	brain angioma	semapv:ManualMappingCuration	2023-11-19
MONDO:0003429	functioning pituitary gland adenoma	skos:exactMatch	DOID:5395	functioning pituitary adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003430	prolactin producing pituitary tumor	skos:exactMatch	DOID:5396	prolactin producing pituitary tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003431	lipoadenoma	skos:exactMatch	DOID:5398	lipoadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003434	vaginal adenoma	skos:exactMatch	DOID:5402	vaginal adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003438	combined small cell lung carcinoma	skos:exactMatch	DOID:5421	lung combined type small cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003439	urinary bladder villous adenoma	skos:exactMatch	DOID:5427	urinary bladder villous adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003441	dystonic disorder	skos:exactMatch	DOID:543	dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0003442	bladder papillary urothelial neoplasm	skos:exactMatch	DOID:5432	bladder papillary transitional cell neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003443	papillary urothelial neoplasm	skos:exactMatch	DOID:5433	urinary tract papillary transitional cell benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003444	intrahepatic bile duct adenoma	skos:exactMatch	DOID:5437	intrahepatic bile duct adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003445	extrahepatic bile duct adenoma	skos:exactMatch	DOID:5438	extrahepatic bile duct adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003446	papillary hidradenoma	skos:exactMatch	DOID:5439	papillary hidradenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003448	benign spiradenoma	skos:exactMatch	DOID:5444	spiradenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003450	eccrine papillary adenoma	skos:exactMatch	DOID:5446	eccrine papillary adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003453	conjunctival intraepithelial neoplasm	skos:exactMatch	DOID:5465	conjunctival intraepithelial neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003454	conjunctival cancer	skos:exactMatch	DOID:5467	conjunctival cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003455	bile duct papillary neoplasm	skos:exactMatch	DOID:5468	biliary papillomatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003458	uterine corpus adenofibroma	skos:exactMatch	DOID:5475	uterine corpus adenofibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003461	fallopian tube serous adenofibroma	skos:exactMatch	DOID:5478	fallopian tube adenofibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003464	cystadenofibroma	skos:exactMatch	DOID:5482	cystadenofibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003466	spindle cell synovial sarcoma	skos:exactMatch	DOID:5487	spindle cell synovial sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003467	mediastinum synovial sarcoma	skos:exactMatch	DOID:5488	mediastinum synovial sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003468	biphasic synovial sarcoma	skos:exactMatch	DOID:5492	biphasic synovial sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003472	lice infestation	skos:exactMatch	DOID:5502	lice infestation	semapv:ManualMappingCuration	2023-03-17
MONDO:0003473	spinal cord ependymoma	skos:exactMatch	DOID:5503	spinal cord ependymoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003477	brain stem ependymoma	skos:exactMatch	DOID:5508	brain stem ependymoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003478	childhood ependymoma	skos:exactMatch	DOID:5509	childhood ependymoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003480	pineal region dysgerminoma	skos:exactMatch	DOID:5510	pineal dysgerminoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003482	Pediculus humanus corporis infestation	skos:exactMatch	DOID:5513	Pediculus humanus corporis infestation	semapv:ManualMappingCuration	2024-04-21
MONDO:0003490	ampulla of vater squamous cell carcinoma	skos:exactMatch	DOID:5527	ampulla of Vater squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003492	lacrimal gland squamous cell carcinoma	skos:exactMatch	DOID:5529	lacrimal gland squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003495	ovarian squamous cell neoplasm	skos:exactMatch	DOID:5532	ovarian squamous cell neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003497	renal pelvis squamous cell carcinoma	skos:exactMatch	DOID:5534	renal pelvis squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003500	squamous cell bile duct carcinoma	skos:exactMatch	DOID:5537	squamous cell bile duct carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003501	external ear squamous cell carcinoma	skos:exactMatch	DOID:5538	external ear squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003502	ureter squamous cell carcinoma	skos:exactMatch	DOID:5539	ureter squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003503	fallopian tube squamous cell carcinoma	skos:exactMatch	DOID:5540	fallopian tube squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003504	anal canal neuroendocrine neoplasm	skos:exactMatch	DOID:5545	anal neuroendocrine tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003506	pulmonary artery choriocarcinoma	skos:exactMatch	DOID:5547	pulmonary artery choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003509	pineal region choriocarcinoma	skos:exactMatch	DOID:5553	pineal region choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003510	malignant testicular germ cell tumor	skos:exactMatch	DOID:5556	testicular malignant germ cell cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003512	mediastinal mesenchymal tumor	skos:exactMatch	DOID:5560	mediastinal mesenchymal tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003513	gastric teratoma	skos:exactMatch	DOID:5561	gastric teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003514	malignant teratoma	skos:exactMatch	DOID:5563	malignant teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003515	fallopian tube teratoma	skos:exactMatch	DOID:5564	fallopian tube teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003516	adult teratoma	skos:exactMatch	DOID:5565	adult teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003518	mediastinum teratoma	skos:exactMatch	DOID:5568	mediastinum teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003519	malignant syringoma	skos:exactMatch	DOID:5569	malignant syringoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003523	gastrin-producing neuroendocrine tumor	skos:exactMatch	DOID:5577	gastrinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003524	gastric gastrin-producing neuroendocrine tumor	skos:exactMatch	DOID:5579	gastric gastrinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003525	pancreatic gastrin-producing neuroendocrine tumor	skos:exactMatch	DOID:5580	pancreatic gastrinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003529	acute pyelonephritis	skos:exactMatch	DOID:559	acute pyelonephritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003531	papillary eccrine carcinoma	skos:exactMatch	DOID:5591	eccrine papillary adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003532	breast papillary carcinoma	skos:exactMatch	DOID:5592	breast papillary carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003534	papillary thymic adenocarcinoma	skos:exactMatch	DOID:5595	papillary thymic adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003535	fallopian tube papillary adenocarcinoma	skos:exactMatch	DOID:5597	fallopian tube papillary adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003541	adult acute lymphoblastic leukemia	skos:exactMatch	DOID:5604	adult acute lymphocytic leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0003544	spinal cord cancer	skos:exactMatch	DOID:5612	spinal cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003546	third cranial nerve disorder	skos:exactMatch	DOID:562	third cranial nerve disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003548	adenosquamous breast carcinoma	skos:exactMatch	DOID:5623	adenosquamous breast carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003549	adenosquamous bile duct carcinoma	skos:exactMatch	DOID:5624	adenosquamous bile duct carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003550	esophageal adenosquamous carcinoma	skos:exactMatch	DOID:5625	esophageal adenosquamous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003551	thymic adenosquamous carcinoma	skos:exactMatch	DOID:5626	thymus adenosquamous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003553	ampulla of vater adenosquamous carcinoma	skos:exactMatch	DOID:5628	ampulla of Vater adenosquamous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003554	adenosquamous colon carcinoma	skos:exactMatch	DOID:5629	adenosquamous colon carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003555	Bartholin gland adenosquamous carcinoma	skos:exactMatch	DOID:5630	Bartholin's gland adenosquamous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003558	adenosquamous prostate carcinoma	skos:exactMatch	DOID:5634	adenosquamous prostate carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003561	malignant giant cell tumor of soft parts	skos:exactMatch	DOID:5638	malignant giant cell tumor of soft parts	semapv:ManualMappingCuration	2023-03-17
MONDO:0003565	urethral villous adenoma	skos:exactMatch	DOID:5643	urethral villous adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003569	cranial nerve neuropathy	skos:exactMatch	DOID:5656	cranial nerve disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003572	nasopharyngeal type undifferentiated carcinoma	skos:exactMatch	DOID:5660	lymphoepithelioma-like carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003574	external ear cancer	skos:exactMatch	DOID:5665	external ear cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0003578	extragonadal nonseminomatous germ cell tumor	skos:exactMatch	DOID:5677	malignant extragonadal nonseminomatous germ cell tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003582	hereditary breast ovarian cancer syndrome	skos:exactMatch	DOID:5683	hereditary breast ovarian cancer syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0003585	adult liposarcoma	skos:exactMatch	DOID:5693	adult liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003586	esophagus liposarcoma	skos:exactMatch	DOID:5694	esophagus liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003587	pediatric liposarcoma	skos:exactMatch	DOID:5695	childhood liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003588	larynx liposarcoma	skos:exactMatch	DOID:5696	larynx liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003589	liposarcoma of the ovary	skos:exactMatch	DOID:5697	liposarcoma of the ovary	semapv:ManualMappingCuration	2024-04-21
MONDO:0003591	kidney liposarcoma	skos:exactMatch	DOID:5699	kidney liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003592	gastric liposarcoma	skos:exactMatch	DOID:5700	gastric liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003593	breast liposarcoma	skos:exactMatch	DOID:5701	breast liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003594	mixed liposarcoma	skos:exactMatch	DOID:5703	mixed liposarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003596	spindle cell liposarcoma	skos:exactMatch	DOID:5705	spindle cell liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003599	vulvar liposarcoma	skos:exactMatch	DOID:5711	vulvar liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003600	cutaneous liposarcoma	skos:exactMatch	DOID:5712	cutaneous liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003601	mediastinum liposarcoma	skos:exactMatch	DOID:5713	mediastinum liposarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003604	functioning pituitary gland neoplasm	skos:exactMatch	DOID:5716	hormone producing pituitary cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003606	adrenal medulla cancer	skos:exactMatch	DOID:5719	adrenal medulla cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003607	neuritis of upper limb	skos:exactMatch	DOID:572	mononeuritis of upper limb and mononeuritis multiplex	semapv:ManualMappingCuration	2023-03-17
MONDO:0003608	optic atrophy	skos:exactMatch	DOID:5723	optic atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0003611	uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease	skos:exactMatch	DOID:5726	uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0003612	uterine ligament cancer	skos:exactMatch	DOID:5727	uterine ligament cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0003617	chronic salpingitis	skos:exactMatch	DOID:5731	chronic salpingitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003619	salpingitis	skos:exactMatch	DOID:5733	salpingitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003624	acinic cell breast carcinoma	skos:exactMatch	DOID:5743	acinic cell breast carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003626	uterine ligament serous adenocarcinoma	skos:exactMatch	DOID:5747	uterine ligament serous adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003627	rheumatic pulmonary valve disease	skos:exactMatch	DOID:5748	rheumatic pulmonary valve disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0003630	pancreatic serous cystadenocarcinoma	skos:exactMatch	DOID:5751	pancreatic serous cystadenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003631	cervical serous adenocarcinoma	skos:exactMatch	DOID:5752	cervical serous adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003632	endocervicitis	skos:exactMatch	DOID:5757	endocervicitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003633	malignant mesenchymoma	skos:exactMatch	DOID:5758	malignant mesenchymoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003635	sebaceous breast carcinoma	skos:exactMatch	DOID:5760	sebaceous breast carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003636	vulvar sebaceous carcinoma	skos:exactMatch	DOID:5761	vulvar sebaceous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003638	lung meningioma	skos:exactMatch	DOID:5764	lung meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003641	central nervous system hematopoietic neoplasm	skos:exactMatch	DOID:5772	central nervous system hematologic cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003644	cavernous hemangioma of colon	skos:exactMatch	DOID:5775	cavernous hemangioma of colon	semapv:ManualMappingCuration	2024-04-21
MONDO:0003646	rectum neuroendocrine neoplasm	skos:exactMatch	DOID:5777	rectum neuroendocrine neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003649	esophageal neuroendocrine tumor	skos:exactMatch	DOID:5784	esophageal neuroendocrine tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003654	childhood parosteal osteosarcoma	skos:exactMatch	DOID:5809	childhood parosteal osteogenic sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003656	hemoglobinuria	skos:exactMatch	DOID:582	hemoglobinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0003659	pediatric lymphoma	skos:exactMatch	DOID:5823	childhood lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003660	adult lymphoma	skos:exactMatch	DOID:5825	adult lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003661	breast lymphoma	skos:exactMatch	DOID:5826	breast lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003663	uterine ligament endometrioid adenocarcinoma	skos:exactMatch	DOID:5829	uterine ligament endometrioid adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003666	fallopian tube endometrioid adenocarcinoma	skos:exactMatch	DOID:5831	fallopian tube endometrioid adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003668	extragonadal seminoma	skos:exactMatch	DOID:5838	extragonadal seminoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003680	periosteal chondrosarcoma	skos:exactMatch	DOID:5859	periosteal chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003680	periosteal chondrosarcoma	skos:exactMatch	DOID:5866	juxtacortical chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003681	myxoid chondrosarcoma	skos:exactMatch	DOID:5861	myxoid chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003684	clear cell chondrosarcoma	skos:exactMatch	DOID:5867	clear cell chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003685	retroperitoneal germ cell neoplasm	skos:exactMatch	DOID:5874	retroperitoneal germ cell neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003686	apocrine sweat gland neoplasm	skos:exactMatch	DOID:5876	apocrine sweat gland neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003687	endocardium cancer	skos:exactMatch	DOID:5877	endocardium cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0003688	well differentiated papillary mesothelioma	skos:exactMatch	DOID:5884	benign intermediate mesothelioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003689	familial hemolytic anemia	skos:exactMatch	DOID:589	congenital hemolytic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0003690	adult anaplastic ependymoma	skos:exactMatch	DOID:5890	malignant adult ependymoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003691	childhood malignant mesenchymoma	skos:exactMatch	DOID:5893	childhood malignant mesenchymoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003692	adult malignant mesenchymoma	skos:exactMatch	DOID:5894	adult malignant mesenchymoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003697	non-invasive verrucous carcinoma of the penis	skos:exactMatch	DOID:5907	penis non-invasive verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003698	penis verrucous carcinoma	skos:exactMatch	DOID:5908	penis verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003700	brachial plexus neoplasm	skos:exactMatch	DOID:5913	brachial plexus neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003704	uterine corpus diffuse leiomyomatosis	skos:exactMatch	DOID:5916	uterine corpus leiomyomatosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003704	uterine corpus diffuse leiomyomatosis	skos:exactMatch	DOID:5917	uterine corpus diffuse leiomyomatosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003710	ovarian mixed germ cell neoplasm	skos:exactMatch	DOID:5936	ovarian mixed germ cell neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003714	bladder urachal squamous cell carcinoma	skos:exactMatch	DOID:5957	bladder urachal squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003715	bladder urachal carcinoma	skos:exactMatch	DOID:5958	bladder urachal carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003716	renal pelvis papillary urothelial carcinoma	skos:exactMatch	DOID:5973	kidney pelvis papillary carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003717	renal pelvis papillary tumor	skos:exactMatch	DOID:5975	renal pelvis papillary tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003719	renal pelvis neoplasm	skos:exactMatch	DOID:5977	renal pelvis benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003720	kidney fibrosarcoma	skos:exactMatch	DOID:5982	kidney fibrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003721	kidney osteogenic sarcoma	skos:exactMatch	DOID:5983	kidney osteogenic sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003724	non-proliferative fibrocystic change of the breast	skos:exactMatch	DOID:5997	non-proliferative fibrocystic change of the breast	semapv:ManualMappingCuration	2023-03-17
MONDO:0003728	breast fibrosarcoma	skos:exactMatch	DOID:6001	breast fibrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003731	adult central nervous system teratoma	skos:exactMatch	DOID:6015	adult central nervous system teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003734	adult central nervous system immature teratoma	skos:exactMatch	DOID:6018	adult central nervous system immature teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003735	central nervous system immature teratoma	skos:exactMatch	DOID:6019	central nervous system immature teratoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003739	selective immunoglobulin deficiency disease	skos:exactMatch	DOID:6025	selective immunoglobulin deficiency disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003741	juvenile type testicular granulosa cell tumor	skos:exactMatch	DOID:6032	juvenile type testicular granulosa cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003742	heart fibrosarcoma	skos:exactMatch	DOID:6033	heart fibrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003743	heart malignant hemangiopericytoma	skos:exactMatch	DOID:6034	heart malignant hemangiopericytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003744	spindle cell intraocular melanoma	skos:exactMatch	DOID:6037	spindle cell intraocular melanoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003745	choroid spindle cell melanoma	skos:exactMatch	DOID:6041	choroid spindle cell melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003746	ciliary body spindle cell melanoma	skos:exactMatch	DOID:6043	ciliary body spindle cell melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003750	childhood central nervous system germ cell tumor	skos:exactMatch	DOID:6052	central nervous system childhood germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003751	childhood germ cell tumor	skos:exactMatch	DOID:6053	childhood germ cell cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003755	urinary tract non-invasive transitional cell neoplasm	skos:exactMatch	DOID:6065	urinary tract non-invasive transitional cell neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003756	ovarian mucinous neoplasm	skos:exactMatch	DOID:6067	ovarian mucinous neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003758	childhood testicular germ cell tumor	skos:exactMatch	DOID:6082	childhood testicular germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003759	childhood ovarian yolk sac tumor	skos:exactMatch	DOID:6083	childhood ovarian endodermal sinus tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003760	pediatric ovarian germ cell tumor	skos:exactMatch	DOID:6084	childhood ovarian germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003761	leptomeningeal melanoma	skos:exactMatch	DOID:6085	meningeal melanoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003762	malignant leptomeningeal tumor	skos:exactMatch	DOID:6086	malignant leptomeningeal neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003764	pediatric leptomeningeal melanoma	skos:exactMatch	DOID:6089	childhood leptomeningeal melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003766	thalamic cancer	skos:exactMatch	DOID:6098	thalamic neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0003769	herpetic gastritis	skos:exactMatch	DOID:6102	herpetic gastritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003772	cerebral meningioma	skos:exactMatch	DOID:6112	cerebral meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003776	renal pelvis inverted papilloma	skos:exactMatch	DOID:6118	renal pelvis inverted papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003777	renal pelvis urothelial papilloma	skos:exactMatch	DOID:6119	renal pelvis urothelial papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003778	inborn error of immunity	skos:exactMatch	DOID:612	primary immunodeficiency disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003783	lymphopenia	skos:exactMatch	DOID:614	lymphopenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0003784	nasal cavity carcinoma in situ	skos:exactMatch	DOID:6148	nasal cavity carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0003786	childhood testicular choriocarcinoma	skos:exactMatch	DOID:6160	childhood choriocarcinoma of the testis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003787	childhood testicular mixed germ cell cancer	skos:exactMatch	DOID:6161	childhood testicular mixed germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0003788	childhood embryonal testis carcinoma	skos:exactMatch	DOID:6162	childhood embryonal testis carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003789	hereditary papillary renal cell carcinoma	skos:exactMatch	DOID:6163	familial renal papillary carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003796	rectum Kaposi sarcoma	skos:exactMatch	DOID:6190	rectum Kaposi's sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003801	corneal intraepithelial neoplasm	skos:exactMatch	DOID:6198	corneal intraepithelial neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003802	cornea cancer	skos:exactMatch	DOID:6199	cornea cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0003805	malignant pericardial mesothelioma	skos:exactMatch	DOID:6201	pericardial mesothelioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003808	mediastinal extraskeletal osteosarcoma	skos:exactMatch	DOID:6208	mediastinal osteogenic sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003809	malignant mediastinum hemangiopericytoma	skos:exactMatch	DOID:6209	malignant mediastinum hemangiopericytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003812	ovarian endometrial cancer	skos:exactMatch	DOID:6212	ovarian endometrial cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0003813	ovarian papillary tumor	skos:exactMatch	DOID:6214	ovarian papillary neoplasm	semapv:ManualMappingCuration	2023-11-19
MONDO:0003816	articular cartilage disorder	skos:exactMatch	DOID:6227	articular cartilage disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003819	childhood teratoma of the ovary	skos:exactMatch	DOID:6230	childhood teratoma of the ovary	semapv:ManualMappingCuration	2024-04-21
MONDO:0003821	ovarian biphasic or triphasic teratoma	skos:exactMatch	DOID:6232	ovarian biphasic or triphasic teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003822	non-invasive bladder papillary urothelial neoplasm	skos:exactMatch	DOID:6239	non-invasive bladder papillary urothelial neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003824	hereditary kidney oncocytoma	skos:exactMatch	DOID:6244	familial renal oncocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003825	kidney oncocytoma	skos:exactMatch	DOID:6245	renal oncocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003826	mediastinum seminoma	skos:exactMatch	DOID:6249	mediastinum seminoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003827	transient hypogammaglobulinemia	skos:exactMatch	DOID:625	transient hypogammaglobulinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0003828	growth hormone-producing pituitary gland carcinoma	skos:exactMatch	DOID:6256	malignant growth hormone secreting neoplasm of pituitary	semapv:ManualMappingCuration	2024-04-21
MONDO:0003832	complement deficiency	skos:exactMatch	DOID:626	complement deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0003835	gastric cardia adenocarcinoma	skos:exactMatch	DOID:6271	gastric cardia adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003837	TSH producing pituitary tumor	skos:exactMatch	DOID:6275	TSH producing pituitary tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0003840	epicardium lipoma	skos:exactMatch	DOID:6284	epicardium lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003841	heart lipoma	skos:exactMatch	DOID:6285	heart lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003842	childhood cerebellar astrocytic neoplasm	skos:exactMatch	DOID:6286	childhood cerebellar astrocytic neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0003843	cerebral hemisphere lipoma	skos:exactMatch	DOID:6291	cerebral hemisphere lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003844	central nervous system lipoma	skos:exactMatch	DOID:6293	central nervous system lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003846	viral esophagitis	skos:exactMatch	DOID:6297	viral esophagitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0003853	Bartholin gland adenocarcinoma	skos:exactMatch	DOID:6316	Bartholin's gland adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003856	adult malignant hemangiopericytoma	skos:exactMatch	DOID:6332	adult malignant hemangiopericytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003861	vulvar eccrine adenocarcinoma	skos:exactMatch	DOID:6339	vulvar eccrine adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003865	acral lentiginous melanoma	skos:exactMatch	DOID:6367	acral lentiginous melanoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003866	liver extraskeletal osteosarcoma	skos:exactMatch	DOID:6370	hepatic osteogenic sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003869	childhood brain stem glioma	skos:exactMatch	DOID:6383	childhood brain stem glioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003870	childhood brainstem astrocytoma	skos:exactMatch	DOID:6386	childhood brainstem astrocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003874	ovarian serous surface papillary adenocarcinoma	skos:exactMatch	DOID:6408	ovary papillary carcinoma	semapv:ManualMappingCuration	2023-11-19
MONDO:0003876	eyelid carcinoma	skos:exactMatch	DOID:6425	eyelid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003878	malignant choroid melanoma	skos:exactMatch	DOID:6438	malignant choroid melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003881	vulvar apocrine adenocarcinoma	skos:exactMatch	DOID:6448	vulvar apocrine adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003882	central nervous system fibrosarcoma	skos:exactMatch	DOID:6451	central nervous system fibrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003884	lipoma of the rectum	skos:exactMatch	DOID:6459	rectal lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003885	colorectal lipoma	skos:exactMatch	DOID:6460	large intestine lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003886	mucinous cystadenofibroma	skos:exactMatch	DOID:6468	mucinous cystadenofibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003887	ovarian mucinous adenofibroma	skos:exactMatch	DOID:6469	ovarian mucinous adenofibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003890	infiltrating bladder urothelial carcinoma	skos:exactMatch	DOID:6477	invasive bladder transitional cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003891	bladder signet ring cell adenocarcinoma	skos:exactMatch	DOID:6481	bladder signet ring cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003892	acinar lung adenocarcinoma	skos:exactMatch	DOID:6482	lung acinar adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003896	breast capillary hemangioma	skos:exactMatch	DOID:6491	breast capillary hemangioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003897	breast epithelioid hemangioma	skos:exactMatch	DOID:6492	breast epithelioid hemangioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003898	pediatric myxoid chondrosarcoma	skos:exactMatch	DOID:6494	childhood myxoid chondrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003899	adult myxoid chondrosarcoma	skos:exactMatch	DOID:6495	adult myxoid chondrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003901	cerebellar hemangioblastoma	skos:exactMatch	DOID:6500	cerebellar angioblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003902	brain stem hemangioblastoma	skos:exactMatch	DOID:6501	brain stem angioblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003909	Bartholin gland adenomyoma	skos:exactMatch	DOID:6518	Bartholin's gland adenomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003911	ciliary body mixed cell melanoma	skos:exactMatch	DOID:6523	ciliary body mixed cell melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003912	malignant ciliary body melanoma	skos:exactMatch	DOID:6524	malignant ciliary body melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003913	choroid mixed cell melanoma	skos:exactMatch	DOID:6525	choroid mixed cell melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003915	cortical thymoma	skos:exactMatch	DOID:6530	thymoma type B2	semapv:ManualMappingCuration	2023-03-17
MONDO:0003916	overnutrition	skos:exactMatch	DOID:654	overnutrition	semapv:ManualMappingCuration	2023-03-17
MONDO:0003917	heart lymphoma	skos:exactMatch	DOID:6547	heart lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003922	ovarian clear cell malignant adenofibroma	skos:exactMatch	DOID:6554	ovarian clear cell malignant adenofibroma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003923	ethmoid sinus Schneiderian papilloma	skos:exactMatch	DOID:6559	ethmoid sinus Schneiderian papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003925	ethmoid sinus inverted papilloma	skos:exactMatch	DOID:6562	ethmoid sinus inverted papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003926	neurilemmoma of the pleura	skos:exactMatch	DOID:6564	neurilemmoma of the pleura	semapv:ManualMappingCuration	2024-04-21
MONDO:0003930	non-invasive bladder urothelial carcinoma	skos:exactMatch	DOID:6571	non-invasive bladder urothelial carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003931	childhood optic tract astrocytoma	skos:exactMatch	DOID:6575	childhood optic tract astrocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003932	childhood optic nerve glioma	skos:exactMatch	DOID:6576	childhood optic nerve glioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003934	breast apocrine carcinoma	skos:exactMatch	DOID:6581	breast apocrine carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003936	invasive tubular breast carcinoma	skos:exactMatch	DOID:6587	breast tubular carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003937	spondylitis	skos:exactMatch	DOID:6590	spondylitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0003939	muscle tissue disorder	skos:exactMatch	DOID:0080000	muscular disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003939	muscle tissue disorder	skos:exactMatch	DOID:66	muscle tissue disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0003944	endobronchial leiomyoma	skos:exactMatch	DOID:6608	endobronchial leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003945	bone epithelioid hemangioma	skos:exactMatch	DOID:6610	bone epithelioid hemangioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003946	vaginal villous adenoma	skos:exactMatch	DOID:6613	vaginal villous adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003947	hyper-IgM syndrome	skos:exactMatch	DOID:0080544	hyper IgM syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0003948	cerebral hemangioma	skos:exactMatch	DOID:6621	cerebral angioma	semapv:ManualMappingCuration	2023-11-19
MONDO:0003950	nipple carcinoma	skos:exactMatch	DOID:6629	nipple carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003951	scrotal hemangioma	skos:exactMatch	DOID:663	scrotal angioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003952	adult central nervous system choriocarcinoma	skos:exactMatch	DOID:6634	adult central nervous system choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003953	pediatric CNS choriocarcinoma	skos:exactMatch	DOID:6639	childhood CNS choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003954	angiokeratoma of Fordyce	skos:exactMatch	DOID:664	angiokeratoma of Fordyce	semapv:ManualMappingCuration	2024-04-21
MONDO:0003957	adult pineoblastoma	skos:exactMatch	DOID:6648	adult pineoblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003958	childhood central nervous system immature teratoma	skos:exactMatch	DOID:6654	childhood central nervous system immature teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003959	breast large cell neuroendocrine carcinoma	skos:exactMatch	DOID:6657	breast large cell neuroendocrine carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003960	pulmonary large cell neuroendocrine carcinoma	skos:exactMatch	DOID:6658	pulmonary large cell neuroendocrine carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003976	malignant type AB thymoma	skos:exactMatch	DOID:6723	malignant type AB thymoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003978	colon small cell neuroendocrine carcinoma	skos:exactMatch	DOID:6727	colon small cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003979	intrahepatic bile duct cystadenoma	skos:exactMatch	DOID:6733	intrahepatic bile duct cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003982	bilateral breast carcinoma	skos:exactMatch	DOID:6741	bilateral breast cancer	semapv:ManualMappingCuration	2023-11-19
MONDO:0003987	lung lymphoma	skos:exactMatch	DOID:6760	lung lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0003990	malignant breast myoepithelioma	skos:exactMatch	DOID:6776	breast myoepithelial carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0003997	colon Kaposi sarcoma	skos:exactMatch	DOID:6804	colon Kaposi sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004000	childhood pilocytic astrocytoma	skos:exactMatch	DOID:6812	childhood pilocytic astrocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004001	compartment syndrome	skos:exactMatch	DOID:682	compartment syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0004004	motor nerve neuritis	skos:exactMatch	DOID:683	motor neuritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004007	breast intraductal proliferative lesion	skos:exactMatch	DOID:6839	breast intraductal proliferative lesion	semapv:ManualMappingCuration	2023-03-17
MONDO:0004009	kidney pelvis sarcomatoid transitional cell carcinoma	skos:exactMatch	DOID:6844	kidney pelvis sarcomatoid transitional cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004015	pineal region teratoma	skos:exactMatch	DOID:6856	pineal region teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004021	mediastinal malignant lymphoma	skos:exactMatch	DOID:6868	mediastinal malignant lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004024	spinal cord neuroblastoma	skos:exactMatch	DOID:6871	spinal cord neuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004028	small intestinal fibrosarcoma	skos:exactMatch	DOID:6880	small bowel fibrosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004030	ureter transitional cell carcinoma	skos:exactMatch	DOID:6888	ureter transitional cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004034	eye lymphoma	skos:exactMatch	DOID:6903	eye lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004037	retinal edema	skos:exactMatch	DOID:6929	retinal edema	semapv:ManualMappingCuration	2023-03-17
MONDO:0004040	urinary bladder inverted papilloma	skos:exactMatch	DOID:6932	urinary bladder inverted papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004041	urothelial papilloma	skos:exactMatch	DOID:6933	bladder transitional cell papilloma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004042	urethra inverted papilloma	skos:exactMatch	DOID:6934	urethra inverted papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004043	ureter inverted papilloma	skos:exactMatch	DOID:6935	ureter inverted papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004044	ureter urothelial papilloma	skos:exactMatch	DOID:6936	ureter urothelial papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004046	childhood brain meningioma	skos:exactMatch	DOID:6939	childhood brain meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004048	immature gastric teratoma	skos:exactMatch	DOID:6948	malignant gastric teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004050	telangiectatic osteogenic sarcoma	skos:exactMatch	DOID:6951	telangiectatic osteogenic sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004056	bladder papillary urothelial carcinoma	skos:exactMatch	DOID:6975	bladder urothelial papillary carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004064	iris melanoma	skos:exactMatch	DOID:6994	malignant iris melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004067	gallbladder mucinous adenocarcinoma	skos:exactMatch	DOID:6998	gallbladder mucinous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004069	inborn mitochondrial metabolism disorder	skos:exactMatch	DOID:700	mitochondrial metabolism disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004071	childhood cerebral astrocytoma	skos:exactMatch	DOID:7007	childhood cerebral astrocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004075	infiltrating lipoma	skos:exactMatch	DOID:7014	infiltrating lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004076	tendon sheath lipoma	skos:exactMatch	DOID:7016	tendon sheath lipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004080	glottis squamous cell carcinoma	skos:exactMatch	DOID:7031	glottis squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004081	extrahepatic bile duct clear cell adenocarcinoma	skos:exactMatch	DOID:7032	bile duct clear cell adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004082	childhood immature teratoma of ovary	skos:exactMatch	DOID:7037	childhood immature teratoma of ovary	semapv:ManualMappingCuration	2024-04-21
MONDO:0004085	choroid epithelioid cell melanoma	skos:exactMatch	DOID:7041	choroid epithelioid cell melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004086	ciliary body epithelioid cell melanoma	skos:exactMatch	DOID:7042	ciliary body epithelioid cell melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004087	basaloid large cell lung carcinoma	skos:exactMatch	DOID:7045	basaloid lung carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004088	cervical basaloid carcinoma	skos:exactMatch	DOID:7046	cervical basaloid squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004089	basaloid carcinoma of the penis	skos:exactMatch	DOID:7047	penis basaloid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004090	vulvar basaloid squamous cell carcinoma	skos:exactMatch	DOID:7048	vulvar basaloid squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004091	skin basaloid carcinoma	skos:exactMatch	DOID:7049	basaloid squamous cell skin carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004092	thymic basaloid carcinoma	skos:exactMatch	DOID:7050	thymus basaloid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004093	esophageal basaloid carcinoma	skos:exactMatch	DOID:7051	esophageal basaloid squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004095	B-cell neoplasm	skos:exactMatch	DOID:707	B-cell lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004099	adult cystic teratoma	skos:exactMatch	DOID:7079	adult cystic teratoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004104	splenic manifestation of hairy cell leukemia	skos:exactMatch	DOID:709	splenic manifestation of hairy cell leukemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004105	childhood epithelioid sarcoma	skos:exactMatch	DOID:7095	childhood epithelioid sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004107	splenic manifestation of leukemia	skos:exactMatch	DOID:710	splenic manifestation of leukemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004110	refractory hairy cell leukemia	skos:exactMatch	DOID:711	refractory hairy cell leukemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004111	refractory hematologic cancer	skos:exactMatch	DOID:712	refractory hematologic cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004116	esophageal small cell neuroendocrine carcinoma	skos:exactMatch	DOID:7134	esophagus small cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004117	ampulla of vater small cell neuroendocrine carcinoma	skos:exactMatch	DOID:7136	ampulla of Vater small cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004120	Bartholin gland small cell carcinoma	skos:exactMatch	DOID:7140	Bartholin's gland small cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004125	rectum leiomyoma	skos:exactMatch	DOID:7160	rectal leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004126	thyroiditis	skos:exactMatch	DOID:7166	thyroiditis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004130	anus basaloid carcinoma	skos:exactMatch	DOID:7174	anus basaloid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004131	anal verrucous carcinoma	skos:exactMatch	DOID:7175	anal Buschke-Lowenstein tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004132	anal canal squamous cell carcinoma	skos:exactMatch	DOID:7177	anal canal squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004139	normocytic anemia	skos:exactMatch	DOID:720	normocytic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004148	gallbladder papillary neoplasm with an associated invasive carcinoma	skos:exactMatch	DOID:7221	gallbladder papillary carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004151	spinal meninges cancer	skos:exactMatch	DOID:7224	spinal meninges cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004153	childhood central nervous system embryonal carcinoma	skos:exactMatch	DOID:7231	childhood CNS embryonal cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004155	adult central nervous system embryonal carcinoma	skos:exactMatch	DOID:7233	adult central nervous system embryonal carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004156	pancreatic mucinous cystadenocarcinoma	skos:exactMatch	DOID:7234	mucinous cystadenocarcinoma of pancreas	semapv:ManualMappingCuration	2024-04-21
MONDO:0004163	bladder urachal urothelial carcinoma	skos:exactMatch	DOID:7244	bladder urachal urothelial carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004166	hereditary fallopian tube carcinoma	skos:exactMatch	DOID:7266	familiar fallopian tube carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004168	cribriform variant testicular seminoma	skos:exactMatch	DOID:7269	cribriform variant testicular seminoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004169	premenstrual tension	skos:exactMatch	DOID:727	premenstrual tension	semapv:ManualMappingCuration	2023-03-17
MONDO:0004176	childhood extraosseous osteosarcoma	skos:exactMatch	DOID:7297	childhood extraosseous osteosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004177	benign urethral neoplasm	skos:exactMatch	DOID:730	urethral benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0004180	benign urinary system neoplasm	skos:exactMatch	DOID:731	urinary system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0004183	axonal neuropathy	skos:exactMatch	DOID:7319	axonal neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0004185	ovarian serous cystadenofibroma	skos:exactMatch	DOID:7320	ovarian serous cystadenofibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004187	nodular fasciitis	skos:exactMatch	DOID:7327	pseudosarcomatous fibromatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004188	iris spindle cell melanoma	skos:exactMatch	DOID:7328	iris spindle cell melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004189	esophageal tuberculosis	skos:exactMatch	DOID:7332	esophageal tuberculosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004192	urethra cancer	skos:exactMatch	DOID:734	urethra cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004193	pediatric ovarian dysgerminoma	skos:exactMatch	DOID:7340	childhood ovarian dysgerminoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004196	rectal sarcomatoid carcinoma	skos:exactMatch	DOID:7356	rectum sarcomatoid carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004197	male urethral cancer	skos:exactMatch	DOID:736	male urethral cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004199	vulvar keratinizing squamous cell carcinoma	skos:exactMatch	DOID:7363	vulvar keratinizing squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004202	adrenal medulla carcinoma	skos:exactMatch	DOID:7379	adrenal medulla carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004204	squamous cell skin papilloma	skos:exactMatch	DOID:7380	squamous cell papilloma of skin	semapv:ManualMappingCuration	2024-04-21
MONDO:0004207	pulmonary artery leiomyosarcoma	skos:exactMatch	DOID:7389	pulmonary artery leiomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004215	cutaneous anthrax	skos:exactMatch	DOID:7426	cutaneous anthrax	semapv:ManualMappingCuration	2024-04-21
MONDO:0004216	pineal region germinoma	skos:exactMatch	DOID:7428	pineal region germinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004217	childhood brain germinoma	skos:exactMatch	DOID:7429	childhood brain germinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004221	uterine corpus perivascular epithelioid cell tumor	skos:exactMatch	DOID:7437	uterus perivascular epithelioid cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004222	ovarian clear cell cystadenocarcinoma	skos:exactMatch	DOID:7438	ovarian clear cell cystadenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004223	polyp of middle ear	skos:exactMatch	DOID:7439	polyp of middle ear	semapv:ManualMappingCuration	2024-04-21
MONDO:0004231	spindle cell variant squamous cell breast carcinoma	skos:exactMatch	DOID:7460	spindle cell variant squamous cell breast carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004233	childhood pleomorphic rhabdomyosarcoma	skos:exactMatch	DOID:7463	childhood pleomorphic rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004235	diverticulitis	skos:exactMatch	DOID:7475	diverticulitis	semapv:ManualMappingCuration	2024-02-18
MONDO:0004239	cervical keratinizing squamous cell carcinoma	skos:exactMatch	DOID:7483	cervical keratinizing squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004245	ependymal tumor of brain	skos:exactMatch	DOID:7497	brain ependymoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004247	peptic ulcer disease	skos:exactMatch	DOID:750	peptic ulcer disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004250	extrahepatic bile duct papillary adenoma	skos:exactMatch	DOID:7503	extrahepatic bile duct papillary adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004251	small intestine neoplasm	skos:exactMatch	DOID:7505	small intestine benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0004255	Wolffian adnexal tumor	skos:exactMatch	DOID:7514	Wolffian adnexal neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0004257	childhood central nervous system mixed germ cell tumor	skos:exactMatch	DOID:7516	childhood central nervous system mixed germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004259	endocervical carcinoma	skos:exactMatch	DOID:7519	endocervical carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004263	pediatric infratentorial ependymoblastoma	skos:exactMatch	DOID:7522	childhood infratentorial embryonal tumor with multilayered rosettes, C19MC-altered	semapv:ManualMappingCuration	2023-03-17
MONDO:0004265	acute endometritis	skos:exactMatch	DOID:7528	acute endometritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004270	breast ductal adenoma	skos:exactMatch	DOID:7538	breast ductal adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004272	urinary bladder tuberculosis	skos:exactMatch	DOID:754	bladder tuberculosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004281	vulvar eccrine porocarcinoma	skos:exactMatch	DOID:7565	vulvar eccrine porocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004289	glottis verrucous carcinoma	skos:exactMatch	DOID:7583	glottis verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004292	supraglottis verrucous carcinoma	skos:exactMatch	DOID:7586	supraglottis verrucous carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004293	supraglottis squamous cell carcinoma	skos:exactMatch	DOID:7587	supraglottis squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004294	gestational ovarian choriocarcinoma	skos:exactMatch	DOID:7591	gestational ovarian choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004295	asbestos-related lung carcinoma	skos:exactMatch	DOID:7596	asbestos-related lung carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004301	fibrosarcomatous osteosarcoma	skos:exactMatch	DOID:7603	fibrosarcomatous osteosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004305	parathyroid oncocytic adenoma	skos:exactMatch	DOID:7611	parathyroid oncocytic adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004308	meningeal sarcoma	skos:exactMatch	DOID:7614	meninges sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004310	adult embryonal tumor with multilayered rosettes, c19mc-altered	skos:exactMatch	DOID:7631	adult embryonal tumor with multilayered rosettes, C19MC-altered	semapv:ManualMappingCuration	2024-04-21
MONDO:0004312	suprasellar meningioma	skos:exactMatch	DOID:7634	suprasellar meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004314	malignant cutaneous granular cell skin tumor	skos:exactMatch	DOID:7639	malignant granular cell skin tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004320	adult infiltrating astrocytic neoplasm	skos:exactMatch	DOID:7656	adult infiltrating astrocytic neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0004321	endometrial mixed adenocarcinoma	skos:exactMatch	DOID:7664	endometrial mixed adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004322	non-gestational ovarian choriocarcinoma	skos:exactMatch	DOID:7665	non-gestational ovarian choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004323	muscular atrophy	skos:exactMatch	DOID:767	muscular atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0004324	testicular fibroma	skos:exactMatch	DOID:7675	testicular fibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004328	maxillary sinus adenocarcinoma	skos:exactMatch	DOID:7684	maxillary sinus adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004330	leptomeningeal sarcoma	skos:exactMatch	DOID:7689	leptomeninges sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004331	bladder urachal adenocarcinoma	skos:exactMatch	DOID:7694	bladder urachal adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004333	pancreatic ACTH-producing neuroendocrine tumor	skos:exactMatch	DOID:7697	pancreatic ACTH hormone producing tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004334	non-functional pancreatic neuroendocrine tumor	skos:exactMatch	DOID:7698	non-functioning pancreatic endocrine tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004336	rectal signet ring cell adenocarcinoma	skos:exactMatch	DOID:7707	rectum signet ring adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004338	retinal cell cancer	skos:exactMatch	DOID:771	retinal cell cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004343	pancreatic acinar cell cystadenocarcinoma	skos:exactMatch	DOID:7729	acinar cell cystadenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004346	signet ring cell intrahepatic cholangiocarcinoma	skos:exactMatch	DOID:7733	signet ring cell intrahepatic cholangiocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004348	retinal telangiectasia	skos:exactMatch	DOID:7736	retinal telangiectasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004349	retina lymphoma	skos:exactMatch	DOID:774	retina lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004355	childhood leukemia	skos:exactMatch	DOID:7757	childhood leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004357	carcinoma of supraglottis	skos:exactMatch	DOID:7763	carcinoma of supraglottis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004359	delusional disorder	skos:exactMatch	DOID:778	delusional disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0004360	breast extraskeletal osteosarcoma	skos:exactMatch	DOID:7787	breast osteosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004361	adult spinal cord ependymoma	skos:exactMatch	DOID:7788	adult spinal cord ependymoma	semapv:ManualMappingCuration	2023-11-19
MONDO:0004363	adult spinal cord glioblastoma	skos:exactMatch	DOID:7806	adult spinal cord glioblastoma multiforme	semapv:ManualMappingCuration	2024-04-21
MONDO:0004374	adult extraskeletal osteosarcoma	skos:exactMatch	DOID:7827	adult extraosseous osteosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004378	pediatric cerebral ependymoblastoma	skos:exactMatch	DOID:7841	childhood embryonal tumor with multilayered rosettes, C19MC-altered	semapv:ManualMappingCuration	2024-04-21
MONDO:0004379	female breast carcinoma	skos:exactMatch	DOID:0050671	female breast cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004379	female breast carcinoma	skos:exactMatch	DOID:7843	female breast carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004380	dendritic cell sarcoma	skos:exactMatch	DOID:7849	dendritic cell sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004383	adult central nervous system germinoma	skos:exactMatch	DOID:7867	adult central nervous system germinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004384	maxillary sinus inverted papilloma	skos:exactMatch	DOID:7868	maxillary sinus inverted papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004386	uterine corpus atypical polypoid adenomyoma	skos:exactMatch	DOID:7878	uterine corpus atypical polypoid adenomyoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004389	mite infestation	skos:exactMatch	DOID:7894	mite infestation	semapv:ManualMappingCuration	2023-03-17
MONDO:0004392	intracranial extraskeletal myxoid chondrosarcoma	skos:exactMatch	DOID:7903	intracranial chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004394	maxillary sinus squamous cell carcinoma	skos:exactMatch	DOID:7910	maxillary sinus squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004398	mediastinal schwannoma	skos:exactMatch	DOID:6175	mediastinal neurilemmoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004398	mediastinal schwannoma	skos:exactMatch	DOID:7922	benign mediastinal neurilemmoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004401	testis refractory cancer	skos:exactMatch	DOID:7928	testis refractory cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004404	refractory precursor T-lymphoblastic lymphoma/leukemia	skos:exactMatch	DOID:7936	refractory T lymphoblastic leukemia/lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004406	adult central nervous system mixed germ cell tumor	skos:exactMatch	DOID:7945	adult central nervous system mixed germ cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004410	sarcomatoid penile squamous cell carcinoma	skos:exactMatch	DOID:7958	sarcomatoid penile squamous cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004411	duodenal gastrin-producing neuroendocrine tumor	skos:exactMatch	DOID:7959	duodenal gastrinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004423	central nervous system extraskeletal osteosarcoma	skos:exactMatch	DOID:7994	central nervous system osteosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004427	supraglottis neoplasm	skos:exactMatch	DOID:8002	supraglottis neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0004429	skin meningioma	skos:exactMatch	DOID:8006	skin meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004433	papillary carcinoma of the penis	skos:exactMatch	DOID:8013	penis papillary carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004435	liver fibrosarcoma	skos:exactMatch	DOID:8022	liver fibrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004436	ovarian myxoid liposarcoma	skos:exactMatch	DOID:8023	myxoid liposarcoma of the ovary	semapv:ManualMappingCuration	2024-04-21
MONDO:0004440	pineal region meningioma	skos:exactMatch	DOID:8031	pineal region meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004441	childhood ovarian embryonal carcinoma	skos:exactMatch	DOID:8036	childhood ovarian embryonal carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004450	carotid artery occlusion	skos:exactMatch	DOID:807	carotid artery occlusion	semapv:ManualMappingCuration	2023-11-19
MONDO:0004452	childhood central nervous system germinoma	skos:exactMatch	DOID:8078	childhood central nervous system germinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004456	cocaine abuse	skos:exactMatch	DOID:809	cocaine abuse	semapv:ManualMappingCuration	2024-04-21
MONDO:0004457	maxillary sinus Schneiderian papilloma	skos:exactMatch	DOID:8093	maxillary sinus Schneiderian papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004458	bladder mixed adenocarcinoma	skos:exactMatch	DOID:8096	bladder mixed adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004459	bladder hepatoid adenocarcinoma	skos:exactMatch	DOID:8097	bladder hepatoid adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004461	vaginal tubulovillous adenoma	skos:exactMatch	DOID:8104	vaginal tubulovillous adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004462	extrahepatic bile duct cystadenoma	skos:exactMatch	DOID:8105	extrahepatic bile duct cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004468	anal canal Paget disease	skos:exactMatch	DOID:8119	anal canal Paget's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0004474	gallbladder lymphoma	skos:exactMatch	DOID:8135	gallbladder lymphoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004477	adrenal gland ganglioneuroblastoma	skos:exactMatch	DOID:8140	adrenal gland ganglioneuroblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004479	malignant childhood germ cell neoplasm	skos:exactMatch	DOID:8149	malignant childhood germ cell neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0004483	thyroid gland oncocytic adenoma	skos:exactMatch	DOID:8162	thyroid Hurthle cell adenoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004484	gallbladder melanoma	skos:exactMatch	DOID:8167	gallbladder melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004489	fallopian tube gestational choriocarcinoma	skos:exactMatch	DOID:8186	fallopian tube gestational choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004491	uterine corpus choriocarcinoma	skos:exactMatch	DOID:8187	gestational uterine corpus choriocarcinoma	semapv:ManualMappingCuration	2024-05-19
MONDO:0004491	uterine corpus choriocarcinoma	skos:exactMatch	DOID:8188	uterine corpus choriocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004492	mediastinitis	skos:exactMatch	DOID:819	mediastinitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004497	tertiary syphilis	skos:exactMatch	DOID:8200	tertiary syphilis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004501	fallopian tube cystadenofibroma	skos:exactMatch	DOID:8211	fallopian tube cystadenofibroma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004504	penile urethral cancer	skos:exactMatch	DOID:8223	penile urethral cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004513	adult pleomorphic rhabdomyosarcoma	skos:exactMatch	DOID:8251	adult pleomorphic rhabdomyosarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004514	chronic rhinitis	skos:exactMatch	DOID:8252	chronic rhinitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004517	ureter tuberculosis	skos:exactMatch	DOID:827	ureter tuberculosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004519	synovial angioma	skos:exactMatch	DOID:8274	synovial angioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004521	adult epithelioid sarcoma	skos:exactMatch	DOID:8282	adult epithelioid sarcoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004526	mixed endometrial stromal and smooth muscle tumor	skos:exactMatch	DOID:8302	mixed endometrial stromal and smooth muscle tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0004528	lymph node palisaded myofibroblastoma	skos:exactMatch	DOID:8304	lymph node palisaded myofibroblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004532	auditory system cancer	skos:exactMatch	DOID:833	auditory system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004534	microglandular adenosis of breast	skos:exactMatch	DOID:8335	microglandular adenosis of breast	semapv:ManualMappingCuration	2024-04-21
MONDO:0004535	childhood choriocarcinoma of the ovary	skos:exactMatch	DOID:8336	childhood choriocarcinoma of the ovary	semapv:ManualMappingCuration	2024-04-21
MONDO:0004539	aortic malignant tumor	skos:exactMatch	DOID:8352	aortic malignant tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004545	adult malignant schwannoma	skos:exactMatch	DOID:8369	adult malignant schwannoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004548	adult type testicular granulosa cell tumor	skos:exactMatch	DOID:8394	adult type testicular granulosa cell tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004550	malignant cornea melanoma	skos:exactMatch	DOID:8400	malignant cornea melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004554	childhood kidney angiomyolipoma	skos:exactMatch	DOID:8410	childhood kidney angiomyolipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004555	kidney angiomyolipoma	skos:exactMatch	DOID:8411	kidney angiomyolipoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004557	congenital fibrosarcoma	skos:exactMatch	DOID:8418	congenital fibrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004561	retinal melanoma	skos:exactMatch	DOID:8427	retinal melanoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004565	intestinal obstruction	skos:exactMatch	DOID:8437	intestinal obstruction	semapv:ManualMappingCuration	2023-03-17
MONDO:0004566	postgastrectomy syndrome	skos:exactMatch	DOID:8439	postgastrectomy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0004567	ileus	skos:exactMatch	DOID:8440	ileus	semapv:ManualMappingCuration	2023-03-17
MONDO:0004569	brachial plexus neuropathy from injury	skos:exactMatch	DOID:8443	brachial plexus lesion	semapv:ManualMappingCuration	2023-03-17
MONDO:0004571	intestinal impaction	skos:exactMatch	DOID:8448	intestinal impaction	semapv:ManualMappingCuration	2023-03-17
MONDO:0004573	ariboflavinosis	skos:exactMatch	DOID:8454	riboflavin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0004577	corneal ulcer	skos:exactMatch	DOID:8463	corneal ulcer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004579	retinoschisis	skos:exactMatch	DOID:8465	retinoschisis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004580	retinal degeneration	skos:exactMatch	DOID:8466	retinal degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0004582	rheumatic myocarditis	skos:exactMatch	DOID:8481	rheumatic myocarditis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004583	transient retinal arterial occlusion	skos:exactMatch	DOID:8482	transient retinal arterial occlusion	semapv:ManualMappingCuration	2024-04-21
MONDO:0004586	rheumatoid lung disease	skos:exactMatch	DOID:849	rheumatoid arthritis interstitial lung disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004587	hereditary night blindness	skos:exactMatch	DOID:8498	hereditary night blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0004588	night blindness	skos:exactMatch	DOID:8499	night blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0004593	Bartholin duct cyst	skos:exactMatch	DOID:851	Bartholin's duct cyst	semapv:ManualMappingCuration	2023-03-17
MONDO:0004596	cor pulmonale	skos:exactMatch	DOID:8515	Cor pulmonale	semapv:ManualMappingCuration	2023-03-17
MONDO:0004598	acute cor pulmonale	skos:exactMatch	DOID:8514	acute pulmonary heart disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0004598	acute cor pulmonale	skos:exactMatch	DOID:8517	acute cor pulmonale	semapv:ManualMappingCuration	2024-04-21
MONDO:0004600	monocytic leukemia	skos:exactMatch	DOID:8527	monocytic leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004614	chronic monocytic leukemia	skos:exactMatch	DOID:8593	chronic monocytic leukemia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004616	herpetic whitlow	skos:exactMatch	DOID:8607	herpetic whitlow	semapv:ManualMappingCuration	2024-04-21
MONDO:0004617	recurrent hypersomnia	skos:exactMatch	DOID:8619	recurrent hypersomnia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004618	diplegia of upper limb	skos:exactMatch	DOID:862	diplegia of upper limb	semapv:ManualMappingCuration	2023-03-17
MONDO:0004622	chronic intestinal vascular insufficiency	skos:exactMatch	DOID:8633	chronic intestinal vascular insufficiency	semapv:ManualMappingCuration	2024-04-21
MONDO:0004627	duodenitis	skos:exactMatch	DOID:8643	duodenitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004628	gastroduodenitis	skos:exactMatch	DOID:8644	gastroduodenitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004630	substance-induced psychosis	skos:exactMatch	DOID:8646	substance-induced psychosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004631	tongue cancer	skos:exactMatch	DOID:8649	tongue cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004634	vein disorder	skos:exactMatch	DOID:866	vein disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004636	lip carcinoma in situ	skos:exactMatch	DOID:8661	lip carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004640	alcoholic gastritis	skos:exactMatch	DOID:8680	alcoholic gastritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004641	skin carcinoma in situ	skos:exactMatch	DOID:8687	skin carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0004643	myeloid leukemia	skos:exactMatch	DOID:8692	myeloid leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004647	in situ carcinoma	skos:exactMatch	DOID:8719	in situ carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004649	anaerobic pneumonia	skos:exactMatch	DOID:873	anaerobic pneumonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004650	malignant carotid body paraganglioma	skos:exactMatch	DOID:8731	carotid body cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004651	smallpox	skos:exactMatch	DOID:8736	smallpox	semapv:ManualMappingCuration	2023-03-17
MONDO:0004653	atypical chronic myeloid leukemia, BCR-ABL1 negative	skos:exactMatch	DOID:0060597	atypical chronic myeloid leukemia, BCR-ABL1 negative	semapv:ManualMappingCuration	2023-11-19
MONDO:0004653	atypical chronic myeloid leukemia, BCR-ABL1 negative	skos:exactMatch	DOID:8747	subacute myeloid leukemia	semapv:ManualMappingCuration	2023-11-19
MONDO:0004657	disseminated chorioretinitis	skos:exactMatch	DOID:8787	disseminated chorioretinitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004658	breast carcinoma in situ	skos:exactMatch	DOID:8791	breast carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0004659	eye carcinoma in situ	skos:exactMatch	DOID:8792	eye carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004660	lung carcinoma in situ	skos:exactMatch	DOID:8800	lung carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004661	trachea carcinoma in situ	skos:exactMatch	DOID:8802	trachea carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004663	colon carcinoma in situ	skos:exactMatch	DOID:8826	colon carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0004667	sublingual gland cancer	skos:exactMatch	DOID:8849	sublingual gland cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004669	salivary gland cancer	skos:exactMatch	DOID:8850	salivary gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004670	lupus erythematosus	skos:exactMatch	DOID:8857	lupus erythematosus	semapv:ManualMappingCuration	2023-03-17
MONDO:0004671	penis carcinoma in situ	skos:exactMatch	DOID:8872	penis carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0004674	chorioretinitis	skos:exactMatch	DOID:8886	chorioretinitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004675	mitochondrial encephalomyopathy	skos:exactMatch	DOID:890	mitochondrial encephalomyopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0004678	dermatophytosis	skos:exactMatch	DOID:8913	dermatophytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004679	leukoplakia of vagina	skos:exactMatch	DOID:8920	leukoplakia of vagina	semapv:ManualMappingCuration	2024-04-21
MONDO:0004680	primary thrombocytopenia	skos:exactMatch	DOID:8925	primary thrombocytopenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004681	learning disability	skos:exactMatch	DOID:8927	learning disability	semapv:ManualMappingCuration	2023-03-17
MONDO:0004685	Waldeyer's ring cancer	skos:exactMatch	DOID:8937	Waldeyer's ring cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004686	lattice corneal dystrophy	skos:exactMatch	DOID:8943	lattice corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0004689	inborn metal metabolism disorder	skos:exactMatch	DOID:896	metal metabolism disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0004695	liver lymphoma	skos:exactMatch	DOID:901	liver lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004696	larynx carcinoma in situ	skos:exactMatch	DOID:9011	larynx carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004697	esophageal leukoplakia	skos:exactMatch	DOID:9021	esophageal leukoplakia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004698	intestine carcinoma in situ	skos:exactMatch	DOID:9024	intestine carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0004699	gastrointestinal lymphoma	skos:exactMatch	DOID:903	gastrointestinal lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004700	parotid gland cancer	skos:exactMatch	DOID:9036	parotid gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004702	uterine cervix leukoplakia	skos:exactMatch	DOID:9043	uterine cervix leukoplakia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004703	bladder carcinoma in situ	skos:exactMatch	DOID:9053	bladder carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004705	liver solitary fibrous tumor	skos:exactMatch	DOID:907	liver fibroma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004707	anal canal carcinoma in situ	skos:exactMatch	DOID:9087	anal carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004708	esophagus carcinoma in situ	skos:exactMatch	DOID:9095	esophagus carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004710	uterus carcinoma in situ	skos:exactMatch	DOID:9108	uterus carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0004712	herpes simplex dermatitis	skos:exactMatch	DOID:9123	eczema herpeticum	semapv:ManualMappingCuration	2024-04-21
MONDO:0004715	liver carcinoma in situ	skos:exactMatch	DOID:9132	liver carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004716	stomach carcinoma in situ	skos:exactMatch	DOID:9138	stomach carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004723	liver leiomyoma	skos:exactMatch	DOID:917	liver leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004724	submandibular gland cancer	skos:exactMatch	DOID:9173	submandibular gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004725	rectum carcinoma in situ	skos:exactMatch	DOID:9174	rectum carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0004726	liver inflammatory myofibroblastic tumor	skos:exactMatch	DOID:918	liver inflammatory pseudotumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0004727	vestibule of mouth cancer	skos:exactMatch	DOID:9188	vestibule of mouth cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004730	speech disorder	skos:exactMatch	DOID:92	speech disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0004731	central sleep apnea syndrome	skos:exactMatch	DOID:9220	central sleep apnea	semapv:ManualMappingCuration	2023-03-17
MONDO:0004732	kidney carcinoma in situ	skos:exactMatch	DOID:9234	kidney carcinoma in situ	semapv:ManualMappingCuration	2024-04-21
MONDO:0004736	inborn disorder of amino acid metabolism	skos:exactMatch	DOID:9252	amino acid metabolic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0004737	homocystinuria	skos:exactMatch	DOID:9263	homocystinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0004739	urea cycle disorder	skos:exactMatch	DOID:9267	urea cycle disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0004741	tyrosinemia	skos:exactMatch	DOID:9275	tyrosinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004743	hyperhomocysteinemia	skos:exactMatch	DOID:9279	hyperhomocysteinemia	semapv:ManualMappingCuration	2023-11-19
MONDO:0004746	myopathy of extraocular muscle	skos:exactMatch	DOID:929	myopathy of extraocular muscle	semapv:ManualMappingCuration	2023-03-17
MONDO:0004748	lip disorder	skos:exactMatch	DOID:9297	lip disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004749	myocardium cancer	skos:exactMatch	DOID:9299	myocardium cancer	semapv:ManualMappingCuration	2024-04-21
MONDO:0004750	language disorder	skos:exactMatch	DOID:93	language disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0004751	disease of orbital part of eye adnexa	skos:exactMatch	DOID:930	orbital disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004756	nasal cavity neoplasm	skos:exactMatch	DOID:9310	nasal cavity benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0004757	chronic ethmoidal sinusitis	skos:exactMatch	DOID:9312	chronic ethmoiditis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004763	carotid artery dissection	skos:exactMatch	DOID:9348	carotid artery dissection	semapv:ManualMappingCuration	2023-11-19
MONDO:0004768	keratoconjunctivitis	skos:exactMatch	DOID:9368	keratoconjunctivitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004773	iridocyclitis	skos:exactMatch	DOID:9383	iridocyclitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004774	gonococcal iridocyclitis	skos:exactMatch	DOID:9384	gonococcal iridocyclitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004777	acute laryngitis	skos:exactMatch	DOID:9396	acute laryngitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004782	diabetes insipidus	skos:exactMatch	DOID:9409	diabetes insipidus	semapv:ManualMappingCuration	2023-03-17
MONDO:0004784	allergic asthma	skos:exactMatch	DOID:9415	allergic asthma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004786	chronic cholangitis	skos:exactMatch	DOID:9439	chronic cholangitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004788	cervix squamous papilloma	skos:exactMatch	DOID:9445	cervix squamous papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004789	cholangitis	skos:exactMatch	DOID:9446	cholangitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004790	fatty liver disease	skos:exactMatch	DOID:9452	steatotic liver disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004800	chronic dacryoadenitis	skos:exactMatch	DOID:949	chronic dacryoadenitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004804	dacryoadenitis	skos:exactMatch	DOID:950	dacryoadenitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004805	leukocyte disorder	skos:exactMatch	DOID:9500	leukocyte disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004806	chronic eosinophilic pneumonia	skos:exactMatch	DOID:9502	chronic eosinophilic pneumonia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004810	acute ethmoiditis	skos:exactMatch	DOID:9506	acute ethmoiditis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004812	acute dacryoadenitis	skos:exactMatch	DOID:952	acute dacryoadenitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004816	refractory plasma cell neoplasm	skos:exactMatch	DOID:9544	refractory plasma cell neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0004820	peripheral nerve schwannoma	skos:exactMatch	DOID:956	peripheral nerve schwannoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004821	nasopharyngeal disorder	skos:exactMatch	DOID:9561	nasopharyngeal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004822	bronchiectasis	skos:exactMatch	DOID:9563	bronchiectasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004826	urethral calculus	skos:exactMatch	DOID:9589	urethral calculus	semapv:ManualMappingCuration	2024-04-21
MONDO:0004827	esophagus squamous cell papilloma	skos:exactMatch	DOID:959	esophagus squamous cell papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004828	lower urinary tract calculus	skos:exactMatch	DOID:9590	lower urinary tract calculus	semapv:ManualMappingCuration	2023-03-17
MONDO:0004830	fasciitis	skos:exactMatch	DOID:9598	fasciitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004832	esophagus leiomyoma	skos:exactMatch	DOID:960	esophagus leiomyoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0004843	pathologic nystagmus	skos:exactMatch	DOID:9650	pathologic nystagmus	semapv:ManualMappingCuration	2023-03-17
MONDO:0004844	oral mucosa leukoplakia	skos:exactMatch	DOID:9655	oral mucosa leukoplakia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004847	senile cataract	skos:exactMatch	DOID:9669	senile cataract	semapv:ManualMappingCuration	2023-03-17
MONDO:0004848	ulcerative stomatitis	skos:exactMatch	DOID:9673	ulcerative stomatitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004852	gonococcal keratitis	skos:exactMatch	DOID:9697	gonococcal keratitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004853	gonococcal endophthalmia	skos:exactMatch	DOID:9698	gonococcal endophthalmia	semapv:ManualMappingCuration	2024-04-21
MONDO:0004857	tendinitis	skos:exactMatch	DOID:971	tendinitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004860	vitreous disorder	skos:exactMatch	DOID:9720	vitreous disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004863	purulent endophthalmitis	skos:exactMatch	DOID:9724	purulent endophthalmitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004867	upper respiratory tract disorder	skos:exactMatch	DOID:974	upper respiratory tract disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004869	pelvic varices	skos:exactMatch	DOID:9742	pelvic varices	semapv:ManualMappingCuration	2023-03-17
MONDO:0004874	ganglion or cyst of synovium/tendon/bursa	skos:exactMatch	DOID:9754	ganglion or cyst of synovium/tendon/bursa	semapv:ManualMappingCuration	2023-03-17
MONDO:0004880	bowel dysfunction	skos:exactMatch	DOID:9779	bowel dysfunction	semapv:ManualMappingCuration	2023-03-17
MONDO:0004882	angioid streaks of choroid	skos:exactMatch	DOID:979	angioid streaks of choroid	semapv:ManualMappingCuration	2024-04-21
MONDO:0004884	eye degenerative disorder	skos:exactMatch	DOID:9799	eye degenerative disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004885	choroidal sclerosis	skos:exactMatch	DOID:980	choroidal sclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004891	hyperopia	skos:exactMatch	DOID:9834	hyperopia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004892	refractive error	skos:exactMatch	DOID:9835	refractive error	semapv:ManualMappingCuration	2023-03-17
MONDO:0004897	hypotropia	skos:exactMatch	DOID:9841	hypotropia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004900	peripheral vertigo	skos:exactMatch	DOID:9847	peripheral vertigo	semapv:ManualMappingCuration	2023-03-17
MONDO:0004907	alopecia	skos:exactMatch	DOID:987	alopecia	semapv:ManualMappingCuration	2023-03-17
MONDO:0004910	mitral valve prolapse	skos:exactMatch	DOID:988	mitral valve prolapse	semapv:ManualMappingCuration	2023-11-19
MONDO:0004917	internal hordeolum	skos:exactMatch	DOID:9908	internal hordeolum	semapv:ManualMappingCuration	2023-03-17
MONDO:0004923	chronic inflammation of lacrimal passage	skos:exactMatch	DOID:9935	chronic inflammation of lacrimal passage	semapv:ManualMappingCuration	2024-04-21
MONDO:0004924	chronic canaliculitis	skos:exactMatch	DOID:9936	chronic canaliculitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004928	lymph node disorder	skos:exactMatch	DOID:9942	lymph node disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004933	hypoplastic left heart syndrome	skos:exactMatch	DOID:9955	hypoplastic left heart syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0004934	periostitis	skos:exactMatch	DOID:9957	periostitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0004938	substance dependence	skos:exactMatch	DOID:9973	substance dependence	semapv:ManualMappingCuration	2023-03-17
MONDO:0004943	orbit sarcoma	skos:exactMatch	DOID:9987	orbit sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004944	neurosyphilis	skos:exactMatch	DOID:9988	tertiary neurosyphilis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004975	Alzheimer disease	skos:exactMatch	DOID:10652	Alzheimer's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0004976	amyotrophic lateral sclerosis	skos:exactMatch	DOID:332	amyotrophic lateral sclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0004979	asthma	skos:exactMatch	DOID:2841	asthma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004985	bipolar disorder	skos:exactMatch	DOID:3312	bipolar disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0004986	urinary bladder carcinoma	skos:exactMatch	DOID:4007	bladder carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0004992	cancer	skos:exactMatch	DOID:0050686	organ system cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004992	cancer	skos:exactMatch	DOID:0050687	cell type cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0004992	cancer	skos:exactMatch	DOID:162	cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0005041	glaucoma	skos:exactMatch	DOID:1686	glaucoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0005053	ischemic disease	skos:exactMatch	DOID:326	ischemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0005090	schizophrenia	skos:exactMatch	DOID:5419	schizophrenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0005094	hemangiopericytoma	skos:exactMatch	DOID:264	hemangiopericytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0005129	cataract	skos:exactMatch	DOID:83	cataract	semapv:ManualMappingCuration	2023-03-17
MONDO:0005147	type 1 diabetes mellitus	skos:exactMatch	DOID:9744	type 1 diabetes mellitus	semapv:ManualMappingCuration	2023-03-17
MONDO:0005148	type 2 diabetes mellitus	skos:exactMatch	DOID:9352	type 2 diabetes mellitus	semapv:ManualMappingCuration	2023-03-17
MONDO:0005149	pulmonary hypertension	skos:exactMatch	DOID:6432	pulmonary hypertension	semapv:ManualMappingCuration	2023-03-17
MONDO:0005178	osteoarthritis	skos:exactMatch	DOID:8398	osteoarthritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0005180	Parkinson disease	skos:exactMatch	DOID:14330	Parkinson's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0005184	pancreatic ductal adenocarcinoma	skos:exactMatch	DOID:3498	pancreatic ductal adenocarcinoma	semapv:ManualMappingCuration	2023-12-24
MONDO:0005184	pancreatic ductal adenocarcinoma	skos:exactMatch	DOID:3587	pancreatic ductal carcinoma	semapv:ManualMappingCuration	2023-12-24
MONDO:0005232	large cell carcinoma	skos:exactMatch	DOID:4552	large cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0005271	allergic disease	skos:exactMatch	DOID:1205	allergic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0005277	migraine disorder	skos:exactMatch	DOID:6364	migraine	semapv:ManualMappingCuration	2023-03-17
MONDO:0005299	brain ischemia	skos:exactMatch	DOID:2316	brain ischemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0005301	multiple sclerosis	skos:exactMatch	DOID:2377	multiple sclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0005321	Fuchs' endothelial dystrophy	skos:exactMatch	DOID:11555	Fuchs' endothelial dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0005341	skin basal cell carcinoma	skos:exactMatch	DOID:2513	basal cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0005351	anorexia nervosa	skos:exactMatch	DOID:8689	anorexia nervosa	semapv:ManualMappingCuration	2023-03-17
MONDO:0005374	bone marrow neoplasm	skos:exactMatch	DOID:4960	bone marrow cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0005405	childhood onset asthma	skos:exactMatch	DOID:0080815	childhood-onset asthma	semapv:ManualMappingCuration	2023-04-17
MONDO:0005411	gallbladder cancer	skos:exactMatch	DOID:3121	gallbladder cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0005475	migraine with aura	skos:exactMatch	DOID:10024	migraine with aura	semapv:ManualMappingCuration	2023-03-17
MONDO:0005499	brain glioma	skos:exactMatch	DOID:0060108	brain glioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0005508	hereditary multiple osteochondromas	skos:exactMatch	DOID:206	hereditary multiple exostoses	semapv:ManualMappingCuration	2023-03-17
MONDO:0005514	nanophthalmia	skos:exactMatch	DOID:0080634	nanophthalmos	semapv:ManualMappingCuration	2023-03-17
MONDO:0005575	colorectal cancer	skos:exactMatch	DOID:5672	large intestine cancer	semapv:ManualMappingCuration	2023-08-20
MONDO:0005575	colorectal cancer	skos:exactMatch	DOID:9256	colorectal cancer	semapv:ManualMappingCuration	2023-08-20
MONDO:0005784	hantavirus hemorrhagic fever with renal syndrome	skos:exactMatch	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0005835	Lynch syndrome	skos:exactMatch	DOID:3883	Lynch syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0006037	hydrolethalus syndrome	skos:exactMatch	DOID:0050779	hydrolethalus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0006507	hereditary hemochromatosis	skos:exactMatch	DOID:2352	hemochromatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0006596	photoallergic dermatitis	skos:exactMatch	DOID:3818	photoallergic dermatitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0006715	coronary stenosis	skos:exactMatch	DOID:4248	coronary stenosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007029	branchio-oto-renal syndrome	skos:exactMatch	DOID:14702	branchiootorenal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007032	prune belly syndrome	skos:exactMatch	DOID:0060889	prune belly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007033	abducens nerve palsy	skos:exactMatch	DOID:10865	abducens nerve palsy	semapv:ManualMappingCuration	2024-04-21
MONDO:0007034	Adams-Oliver syndrome	skos:exactMatch	DOID:0060227	Adams-Oliver syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007037	Achondroplasia	skos:exactMatch	DOID:4480	achondroplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007039	neurofibromatosis type 2	skos:exactMatch	DOID:0111252	vestibular schwannomatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007040	Sakati-Nyhan syndrome	skos:exactMatch	DOID:0060359	Sakati-Nyhan syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007042	Saethre-Chotzen syndrome	skos:exactMatch	DOID:14768	Saethre-Chotzen syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007043	Pfeiffer syndrome	skos:exactMatch	DOID:14705	Pfeiffer syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007045	acrofacial dysostosis, Catania type	skos:exactMatch	DOID:0060384	acrofacial dysostosis, Catania type	semapv:ManualMappingCuration	2023-03-17
MONDO:0007055	Acromicric dysplasia	skos:exactMatch	DOID:0111243	acromicric dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007057	Acroosteolysis dominant type	skos:exactMatch	DOID:2736	Hajdu-Cheney syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007059	acrorenal syndrome	skos:exactMatch	DOID:0060347	acrorenal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007064	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency	skos:exactMatch	DOID:5810	adenosine deaminase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0007068	adenylosuccinate lyase deficiency	skos:exactMatch	DOID:0050762	adenylosuccinase lyase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0007072	ADULT syndrome	skos:exactMatch	DOID:0050601	ADULT syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007077	Tietz syndrome	skos:exactMatch	DOID:0090002	Tietz syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007078	pseudohypoparathyroidism type 1A	skos:exactMatch	DOID:0080053	Albright's hereditary osteodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007079	alcohol dependence	skos:exactMatch	DOID:0050741	alcohol dependence	semapv:ManualMappingCuration	2023-03-17
MONDO:0007080	glucocorticoid-remediable aldosteronism	skos:exactMatch	DOID:14080	glucocorticoid-remediable aldosteronism	semapv:ManualMappingCuration	2023-03-17
MONDO:0007083	autosomal dominant palmoplantar keratoderma and congenital alopecia	skos:exactMatch	DOID:0111244	palmoplantar keratoderma and congenital alopecia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0007086	autosomal dominant Alport syndrome	skos:exactMatch	DOID:0110032	autosomal dominant Alport syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007088	Alzheimer disease type 1	skos:exactMatch	DOID:0080348	Alzheimer's disease 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0007093	hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism	skos:exactMatch	DOID:0110053	amelogenesis imperfecta type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0007097	Finnish type amyloidosis	skos:exactMatch	DOID:0050637	Finnish type amyloidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007098	ACys amyloidosis	skos:exactMatch	DOID:0070027	CST3-related cerebral amyloid angiopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007099	familial visceral amyloidosis	skos:exactMatch	DOID:0050636	familial visceral amyloidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007104	amyotrophic lateral sclerosis-parkinsonism-dementia complex	skos:exactMatch	DOID:0111246	amyotrophic lateral sclerosis-parkinsonism/dementia complex 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0007105	frontotemporal dementia and/or amyotrophic lateral sclerosis 1	skos:exactMatch	DOID:0060213	frontotemporal dementia and/or amyotrophic lateral sclerosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007108	anal canal carcinoma	skos:exactMatch	DOID:6126	anal canal carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0007109	congenital dyserythropoietic anemia type 3	skos:exactMatch	DOID:0111399	congenital dyserythropoietic anemia type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0007113	Angelman syndrome	skos:exactMatch	DOID:1932	Angelman syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007118	isolated anhidrosis with normal sweat glands	skos:exactMatch	DOID:0060603	isolated anhidrosis with normal sweat glands	semapv:ManualMappingCuration	2023-11-19
MONDO:0007124	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome	skos:exactMatch	DOID:0090119	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007125	ankyloglossia	skos:exactMatch	DOID:0060604	ankyloglossia	semapv:ManualMappingCuration	2023-11-19
MONDO:0007126	spondyloarthropathy, susceptibility to, 1	skos:exactMatch	DOID:0080603	ankylosing spondylitis 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0007142	Townes-Brocks syndrome	skos:exactMatch	DOID:0050887	Townes-Brocks syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007145	aplasia cutis congenita	skos:exactMatch	DOID:0080661	nonsyndromic aplasia cutis congenita	semapv:ManualMappingCuration	2023-06-18
MONDO:0007152	arrhythmogenic right ventricular dysplasia 1	skos:exactMatch	DOID:0110070	arrhythmogenic right ventricular dysplasia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007154	arteriovenous malformations of the brain	skos:exactMatch	DOID:0060688	arteriovenous malformations of the brain	semapv:ManualMappingCuration	2023-03-17
MONDO:0007158	arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome	skos:exactMatch	DOID:0111608	distal arthrogryposis type 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0007159	arthrogryposis-like hand anomaly-sensorineural deafness syndrome	skos:exactMatch	DOID:0111609	distal arthrogryposis type 6	semapv:ManualMappingCuration	2023-04-17
MONDO:0007160	Stickler syndrome type 1	skos:exactMatch	DOID:0080676	Stickler syndrome 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0007161	spermatogenic failure 2	skos:exactMatch	DOID:0070164	spermatogenic failure 2	semapv:ManualMappingCuration	2023-11-19
MONDO:0007163	episodic ataxia type 2	skos:exactMatch	DOID:0050990	episodic ataxia type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007164	spastic ataxia 1	skos:exactMatch	DOID:0050772	spastic ataxia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007165	spastic ataxia 7	skos:exactMatch	DOID:0050945	spastic ataxia 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0007172	atrial septal defect 1	skos:exactMatch	DOID:0110106	atrial heart septal defect 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007173	atrial septal defect 7	skos:exactMatch	DOID:0110112	atrial heart septal defect 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0007174	Lown-Ganong-Levine syndrome	skos:exactMatch	DOID:13087	Lown-Ganong-Levine syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007176	helicoid peripapillary chorioretinal degeneration	skos:exactMatch	DOID:0111228	Sveinsson chorioretinal atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007182	Machado-Joseph disease	skos:exactMatch	DOID:1440	Machado-Joseph disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0007187	nevoid basal cell carcinoma syndrome	skos:exactMatch	DOID:0070365	nevoid basal cell carcinoma syndrome 1	semapv:ManualMappingCuration	2023-07-09
MONDO:0007187	nevoid basal cell carcinoma syndrome	skos:exactMatch	DOID:2512	nevoid basal cell carcinoma syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007194	familial bicuspid aortic valve	skos:exactMatch	DOID:0080332	bicuspid aortic valve disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0007197	bladder diverticulum	skos:exactMatch	DOID:11353	bladder diverticulum	semapv:ManualMappingCuration	2023-03-17
MONDO:0007201	blepharophimosis, ptosis, and epicanthus inversus syndrome	skos:exactMatch	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007205	diaphyseal medullary stenosis-bone malignancy syndrome	skos:exactMatch	DOID:0080664	diaphyseal medullary stenosis with malignant fibrous histiocytoma	semapv:ManualMappingCuration	2023-04-17
MONDO:0007208	Boomerang dysplasia	skos:exactMatch	DOID:0050680	Boomerang dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007211	brachydactyly-arterial hypertension syndrome	skos:exactMatch	DOID:0111247	hypertension and brachydactyly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007213	Ballard syndrome	skos:exactMatch	DOID:0110963	Ballard syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007214	brachydactyly-preaxial hallux varus syndrome	skos:exactMatch	DOID:0110962	brachydactyly-preaxial hallux varus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007215	brachydactyly type A1	skos:exactMatch	DOID:0110964	brachydactyly type A1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007216	brachydactyly type A2	skos:exactMatch	DOID:0110965	brachydactyly type A2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007218	brachydactyly type A4	skos:exactMatch	DOID:0110967	brachydactyly type A4	semapv:ManualMappingCuration	2023-03-17
MONDO:0007219	Osebold-Remondini syndrome	skos:exactMatch	DOID:0110968	brachydactyly type A6	semapv:ManualMappingCuration	2023-03-17
MONDO:0007220	brachydactyly type B1	skos:exactMatch	DOID:0110969	brachydactyly type B1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007221	brachydactyly type C	skos:exactMatch	DOID:0110970	brachydactyly type C	semapv:ManualMappingCuration	2023-03-17
MONDO:0007223	brachydactyly type E1	skos:exactMatch	DOID:0110972	brachydactyly type E1	semapv:ManualMappingCuration	2024-04-21
MONDO:0007235	branchiooculofacial syndrome	skos:exactMatch	DOID:0050691	branchiooculofacial syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007239	epidermolytic ichthyosis	skos:exactMatch	DOID:4603	epidermolytic hyperkeratosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007240	progressive familial heart block, type 1A	skos:exactMatch	DOID:0111074	progressive familial heart block type IA	semapv:ManualMappingCuration	2024-04-21
MONDO:0007244	Caffey disease	skos:exactMatch	DOID:4257	Caffey disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0007251	campomelic dysplasia	skos:exactMatch	DOID:0050463	campomelic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007252	Gordon syndrome	skos:exactMatch	DOID:0111607	distal arthrogryposis type 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0007254	breast cancer	skos:exactMatch	DOID:1612	breast cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0007266	hypertrophic cardiomyopathy 2	skos:exactMatch	DOID:0110308	hypertrophic cardiomyopathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007268	hypertrophic cardiomyopathy 4	skos:exactMatch	DOID:0110310	hypertrophic cardiomyopathy 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0007269	dilated cardiomyopathy 1A	skos:exactMatch	DOID:0110425	dilated cardiomyopathy 1A	semapv:ManualMappingCuration	2023-03-17
MONDO:0007270	cardiomyopathy, familial restrictive, 1	skos:exactMatch	DOID:0111425	restrictive cardiomyopathy 1	semapv:ManualMappingCuration	2024-02-18
MONDO:0007280	cataract 8 multiple types	skos:exactMatch	DOID:0110228	cataract 8 multiple types	semapv:ManualMappingCuration	2023-03-17
MONDO:0007289	cataract 13 with adult I phenotype	skos:exactMatch	DOID:0110242	cataract 13 with adult i phenotype	semapv:ManualMappingCuration	2023-03-17
MONDO:0007290	cataract 5 multiple types	skos:exactMatch	DOID:0110255	cataract 5 multiple types	semapv:ManualMappingCuration	2023-03-17
MONDO:0007293	leukocyte adhesion deficiency 1	skos:exactMatch	DOID:0110910	leukocyte adhesion deficiency 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007295	childhood epilepsy with centrotemporal spikes	skos:exactMatch	DOID:3329	benign epilepsy with centrotemporal spikes	semapv:ManualMappingCuration	2023-03-17
MONDO:0007296	spinocerebellar ataxia type 31	skos:exactMatch	DOID:0050980	spinocerebellar ataxia type 31	semapv:ManualMappingCuration	2023-03-17
MONDO:0007297	ADan amyloidosis	skos:exactMatch	DOID:0070030	ITM2B-related cerebral amyloid angiopathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007298	spinocerebellar ataxia type 29	skos:exactMatch	DOID:0050978	spinocerebellar ataxia type 29	semapv:ManualMappingCuration	2023-03-17
MONDO:0007301	cerebrocostomandibular syndrome	skos:exactMatch	DOID:0111248	cerebrocostomandibular syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007306	Klippel-Feil syndrome 1, autosomal dominant	skos:exactMatch	DOID:0080589	Klippel-Feil syndrome 1	semapv:ManualMappingCuration	2024-02-18
MONDO:0007307	Charcot-Marie-Tooth disease type 1B	skos:exactMatch	DOID:0110152	Charcot-Marie-Tooth disease type 1B	semapv:ManualMappingCuration	2023-03-17
MONDO:0007308	Charcot-Marie-Tooth disease type 2A1	skos:exactMatch	DOID:0110154	Charcot-Marie-Tooth disease type 2A1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007309	Charcot-Marie-Tooth disease type 1A	skos:exactMatch	DOID:0110148	Charcot-Marie-Tooth disease type 1A	semapv:ManualMappingCuration	2023-03-17
MONDO:0007311	Charcot-Marie-Tooth disease type 1E	skos:exactMatch	DOID:0110153	Charcot-Marie-Tooth disease type 1E	semapv:ManualMappingCuration	2023-03-17
MONDO:0007315	cherubism	skos:exactMatch	DOID:1856	cherubism	semapv:ManualMappingCuration	2023-03-17
MONDO:0007318	Alagille syndrome	skos:exactMatch	DOID:9245	Alagille syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007321	autosomal dominant chondrodysplasia punctata	skos:exactMatch	DOID:0060293	autosomal dominant chondrodysplasia punctata	semapv:ManualMappingCuration	2023-03-17
MONDO:0007335	orofacial cleft 1	skos:exactMatch	DOID:0080395	orofacial cleft 1	semapv:ManualMappingCuration	2024-08-18
MONDO:0007336	isolated cleft palate	skos:exactMatch	DOID:0110213	isolated cleft palate	semapv:ManualMappingCuration	2023-03-17
MONDO:0007337	cleft palate-lateral synechia syndrome	skos:exactMatch	DOID:0080313	cleft palate-lateral synechia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007339	blepharocheilodontic syndrome	skos:exactMatch	DOID:0080344	blepharocheilodontic syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007340	cleidocranial dysplasia 1	skos:exactMatch	DOID:13994	cleidocranial dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007342	clubfoot	skos:exactMatch	DOID:11836	clubfoot	semapv:ManualMappingCuration	2023-03-17
MONDO:0007349	familial cold autoinflammatory syndrome 1	skos:exactMatch	DOID:0090062	familial cold autoinflammatory syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007352	renal coloboma syndrome	skos:exactMatch	DOID:0090006	renal coloboma syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007354	coloboma of optic nerve	skos:exactMatch	DOID:11975	coloboma of optic nerve	semapv:ManualMappingCuration	2023-03-17
MONDO:0007355	uveal coloboma-cleft lip and palate-intellectual disability	skos:exactMatch	DOID:0111249	uveal coloboma-cleft lip and palate-intellectual disability	semapv:ManualMappingCuration	2023-03-17
MONDO:0007361	C1 inhibitor deficiency	skos:exactMatch	DOID:0060002	C1 inhibitor deficiency	semapv:ManualMappingCuration	2023-11-19
MONDO:0007363	congenital contractural arachnodactyly	skos:exactMatch	DOID:0111595	congenital contractural arachnodactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0007367	febrile seizures, familial, 1	skos:exactMatch	DOID:0111307	familial febrile seizures 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0007369	hereditary coproporphyria	skos:exactMatch	DOID:13269	hereditary coproporphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0007374	Schnyder corneal dystrophy	skos:exactMatch	DOID:0060456	Schnyder corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007375	epithelial basement membrane dystrophy	skos:exactMatch	DOID:0060447	epithelial basement membrane dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007376	fleck corneal dystrophy	skos:exactMatch	DOID:0060448	Fleck corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007377	granular corneal dystrophy type I	skos:exactMatch	DOID:0080530	granular corneal dystrophy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007379	Meesmann corneal dystrophy	skos:exactMatch	DOID:0060451	Meesmann corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007381	epithelial recurrent erosion dystrophy	skos:exactMatch	DOID:0070337	epithelial recurrent erosion dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007395	craniofacial-deafness-hand syndrome	skos:exactMatch	DOID:0111336	craniofacial-deafness-hand syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007400	Jackson-Weiss syndrome	skos:exactMatch	DOID:0111337	Jackson-Weiss syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007404	Cri-du-chat syndrome	skos:exactMatch	DOID:12580	Cri-du-Chat syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007405	Crouzon syndrome	skos:exactMatch	DOID:2339	Crouzon syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007410	isolated cryptophthalmia	skos:exactMatch	DOID:0111717	isolated cryptophthalmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007411	cutis laxa, autosomal dominant 1	skos:exactMatch	DOID:0070130	autosomal dominant cutis laxa 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0007412	Beare-Stevenson cutis gyrata syndrome	skos:exactMatch	DOID:0050660	Beare-Stevenson cutis gyrata syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007415	mitochondrial complex III deficiency nuclear type 1	skos:exactMatch	DOID:0080111	mitochondrial complex III deficiency nuclear type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007417	Darier disease	skos:exactMatch	DOID:2734	keratosis follicularis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007420	autosomal dominant deafness - onychodystrophy syndrome	skos:exactMatch	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy	semapv:ManualMappingCuration	2023-04-17
MONDO:0007422	keratoderma hereditarium mutilans	skos:exactMatch	DOID:0111339	Vohwinkel syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007424	autosomal dominant nonsyndromic hearing loss 1	skos:exactMatch	DOID:0110541	autosomal dominant nonsyndromic deafness 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007432	cerebral arteriopathy with subcortical infarcts and leukoencephalopathy	skos:exactMatch	DOID:13945	CADASIL	semapv:ManualMappingCuration	2023-03-17
MONDO:0007434	primary failure of tooth eruption	skos:exactMatch	DOID:0111341	primary failure of tooth eruption	semapv:ManualMappingCuration	2023-03-17
MONDO:0007435	dentatorubral-pallidoluysian atrophy	skos:exactMatch	DOID:0060162	dentatorubral-pallidoluysian atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007445	dermatopathia pigmentosa reticularis	skos:exactMatch	DOID:0111342	dermatopathia pigmentosa reticularis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007450	neurohypophyseal diabetes insipidus	skos:exactMatch	DOID:12388	neurohypophyseal diabetes insipidus	semapv:ManualMappingCuration	2023-03-17
MONDO:0007451	diabetes insipidus, nephrogenic, autosomal	skos:exactMatch	DOID:0081061	nephrogenic diabetes insipidus type 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0007453	maturity-onset diabetes of the young type 2	skos:exactMatch	DOID:0111100	maturity-onset diabetes of the young type 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0007454	type 1 diabetes mellitus 2	skos:exactMatch	DOID:0110741	type 1 diabetes mellitus 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0007470	calvarial doughnut lesions-bone fragility syndrome	skos:exactMatch	DOID:0080721	calvarial doughnut lesions with bone fragility	semapv:ManualMappingCuration	2023-06-18
MONDO:0007471	Doyne honeycomb retinal dystrophy	skos:exactMatch	DOID:0060745	Doyne honeycomb retinal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007473	Duane retraction syndrome	skos:exactMatch	DOID:12557	Duane retraction syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007477	3-M syndrome	skos:exactMatch	DOID:0060241	3-M syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007478	autosomal dominant Kenny-Caffey syndrome	skos:exactMatch	DOID:0080723	Kenny-Caffey syndrome type 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0007481	Leri-Weill dyschondrosteosis	skos:exactMatch	DOID:0060847	Leri-Weill dyschondrosteosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007483	dyschromatosis symmetrica hereditaria	skos:exactMatch	DOID:0060257	dyschromatosis symmetrica hereditaria	semapv:ManualMappingCuration	2023-03-17
MONDO:0007492	early-onset generalized limb-onset dystonia	skos:exactMatch	DOID:0060730	torsion dystonia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007493	torsion dystonia 4	skos:exactMatch	DOID:0090041	torsion dystonia 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0007495	dystonia 5	skos:exactMatch	DOID:0060963	dystonia, DOPA-responsive	semapv:ManualMappingCuration	2024-05-19
MONDO:0007495	dystonia 5	skos:exactMatch	DOID:0090043	DOPA-responsive dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007496	dystonia 12	skos:exactMatch	DOID:0090056	dystonia 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0007507	absence of fingerprints-congenital milia syndrome	skos:exactMatch	DOID:0080725	BASAN syndrome	semapv:ManualMappingCuration	2023-06-18
MONDO:0007509	ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant	skos:exactMatch	DOID:0111663	ectodermal dysplasia 10A	semapv:ManualMappingCuration	2023-03-17
MONDO:0007510	Clouston syndrome	skos:exactMatch	DOID:14693	Clouston syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007514	ectopia lentis 1, isolated, autosomal dominant	skos:exactMatch	DOID:0111150	autosomal dominant isolated ectopia lentis 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0007523	Ehlers-Danlos syndrome, hypermobility type	skos:exactMatch	DOID:14757	Ehlers-Danlos syndrome hypermobility type	semapv:ManualMappingCuration	2023-03-17
MONDO:0007524	autosomal dominant Ehlers-Danlos syndrome, vascular type	skos:exactMatch	DOID:14756	vascular type Ehlers-Danlos syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0007525	Ehlers-Danlos syndrome, arthrochalasia type	skos:exactMatch	DOID:0080727	Ehlers-Danlos syndrome arthrochalasia type 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0007526	Ehlers-Danlos syndrome, spondylodysplastic type	skos:exactMatch	DOID:0050802	Ehlers-Danlos syndrome spondylodysplastic type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007534	Beckwith-Wiedemann syndrome	skos:exactMatch	DOID:5572	Beckwith-Wiedemann syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007537	lateral meningocele syndrome	skos:exactMatch	DOID:0111343	lateral meningocele syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007538	amelogenesis imperfecta, type 3A	skos:exactMatch	DOID:0110055	amelogenesis imperfecta type 3A	semapv:ManualMappingCuration	2023-03-17
MONDO:0007540	multiple endocrine neoplasia type 1	skos:exactMatch	DOID:10017	multiple endocrine neoplasia type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007542	Camurati-Engelmann disease	skos:exactMatch	DOID:4997	Camurati-Engelmann disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0007548	transient bullous dermolysis of the newborn	skos:exactMatch	DOID:0111345	transient bullous dermolysis of the newborn	semapv:ManualMappingCuration	2023-03-17
MONDO:0007549	generalized dominant dystrophic epidermolysis bullosa	skos:exactMatch	DOID:0080224	autosomal dominant dystrophic epidermolysis bullosa	semapv:ManualMappingCuration	2023-03-17
MONDO:0007550	epidermolysis bullosa simplex 1A, generalized severe	skos:exactMatch	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type	semapv:ManualMappingCuration	2023-03-17
MONDO:0007551	epidermolysis bullosa simplex 1C, localized	skos:exactMatch	DOID:0080510	epidermolysis bullosa simplex localized type	semapv:ManualMappingCuration	2023-03-17
MONDO:0007552	pretibial dystrophic epidermolysis bullosa	skos:exactMatch	DOID:0080988	pretibial dystrophic epidermolysis bullosa	semapv:ManualMappingCuration	2023-03-17
MONDO:0007554	epidermolysis bullosa simplex 1B, generalized intermediate	skos:exactMatch	DOID:0080511	epidermolysis bullosa simplex generalized type	semapv:ManualMappingCuration	2023-06-18
MONDO:0007555	pidermolysis bullosa simplex 5A, Ogna type	skos:exactMatch	DOID:0060736	epidermolysis bullosa simplex Ogna type	semapv:ManualMappingCuration	2023-03-17
MONDO:0007556	epidermolysis bullosa simplex 2F, with mottled pigmentation	skos:exactMatch	DOID:0111346	epidermolysis bullosa simplex with mottled pigmentation	semapv:ManualMappingCuration	2023-03-17
MONDO:0007561	multiple epiphyseal dysplasia type 1	skos:exactMatch	DOID:0070303	multiple epiphyseal dysplasia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007562	multiple epiphyseal dysplasia, Beighton type	skos:exactMatch	DOID:0111348	multiple epiphyseal dysplasia with myopia and deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0007566	multiple self-healing squamous epithelioma	skos:exactMatch	DOID:5585	Ferguson-Smith tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0007572	primary familial polycythemia due to EPO receptor mutation	skos:exactMatch	DOID:0060652	familial erythrocytosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007574	spinocerebellar ataxia type 34	skos:exactMatch	DOID:0050981	spinocerebellar ataxia type 34	semapv:ManualMappingCuration	2023-03-17
MONDO:0007576	esophageal cancer	skos:exactMatch	DOID:5041	esophageal cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0007606	fibrodysplasia ossificans progressiva	skos:exactMatch	DOID:13374	fibrodysplasia ossificans progressiva	semapv:ManualMappingCuration	2023-03-17
MONDO:0007614	congenital fibrosis of extraocular muscles	skos:exactMatch	DOID:0080143	congenital fibrosis of the extraocular muscles	semapv:ManualMappingCuration	2023-03-17
MONDO:0007615	laurin-Sandrow syndrome	skos:exactMatch	DOID:0111350	Laurin-Sandrow syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007617	Coffin-Siris syndrome 1	skos:exactMatch	DOID:0070042	Coffin-Siris syndrome 1	semapv:ManualMappingCuration	2024-08-18
MONDO:0007619	isolated congenital adermatoglyphia	skos:exactMatch	DOID:0111357	adermatoglyphia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007621	Floating-Harbor syndrome	skos:exactMatch	DOID:0111358	Floating-Harbor syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007628	foveal hypoplasia 1	skos:exactMatch	DOID:0070530	foveal hypoplasia 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0007630	North Carolina macular dystrophy	skos:exactMatch	DOID:0070439	North Carolina macular dystrophy	semapv:ManualMappingCuration	2024-04-21
MONDO:0007631	chromosome 16p12.1 deletion syndrome, 520kb	skos:exactMatch	DOID:0060399	chromosome 16p12.1 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007635	Frasier syndrome	skos:exactMatch	DOID:0050438	Frasier syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007636	frontorhiny	skos:exactMatch	DOID:0081045	frontonasal dysplasia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0007639	fundus albipunctatus	skos:exactMatch	DOID:11105	fundus albipunctatus	semapv:ManualMappingCuration	2023-03-17
MONDO:0007640	Sorsby fundus dystrophy	skos:exactMatch	DOID:0090114	Sorsby's fundus dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0007646	Gamstorp-Wohlfart syndrome	skos:exactMatch	DOID:0050526	Gamstorp-Wohlfart syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007648	hereditary diffuse gastric adenocarcinoma	skos:exactMatch	DOID:0080764	hereditary diffuse gastric cancer	semapv:ManualMappingCuration	2023-04-17
MONDO:0007656	Gerstmann-Straussler-Scheinker syndrome	skos:exactMatch	DOID:4249	Gerstmann-Straussler-Scheinker syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007662	anterior segment dysgenesis 4	skos:exactMatch	DOID:0080609	anterior segment dysgenesis 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0007669	renal cysts and diabetes syndrome	skos:exactMatch	DOID:0111101	maturity-onset diabetes of the young type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0007672	glomuvenous malformation	skos:exactMatch	DOID:7996	familial glomangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0007686	gray platelet syndrome	skos:exactMatch	DOID:0111044	gray platelet syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007690	aromatase excess syndrome	skos:exactMatch	DOID:0090122	aromatase excess syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007698	hand-foot-genital syndrome	skos:exactMatch	DOID:0060739	hand-foot-genital syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007700	hawkinsinuria	skos:exactMatch	DOID:0111362	hawkinsinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0007705	Heinz body anemia	skos:exactMatch	DOID:0111363	Heinz body anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007716	alpha thalassemia-intellectual disability syndrome type 1	skos:exactMatch	DOID:0110029	alpha thalassemia-intellectual disability syndrome type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007726	hip dysplasia, Beukes type	skos:exactMatch	DOID:0111367	Beukes hip dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007727	autosomal dominant familial periodic fever	skos:exactMatch	DOID:0090018	autosomal dominant familial periodic fever	semapv:ManualMappingCuration	2023-03-17
MONDO:0007732	Holt-Oram syndrome	skos:exactMatch	DOID:0060468	Holt-Oram syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007733	holoprosencephaly 3	skos:exactMatch	DOID:0110875	holoprosencephaly 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0007737	humeroradial synostosis	skos:exactMatch	DOID:0060467	humeroradial synostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007738	spondyloepiphyseal dysplasia with congenital joint dislocations	skos:exactMatch	DOID:0050813	spondyloepiphyseal dysplasia with congenital joint dislocations	semapv:ManualMappingCuration	2023-03-17
MONDO:0007739	Huntington disease	skos:exactMatch	DOID:12858	Huntington's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0007744	cholesterol-ester transfer protein deficiency	skos:exactMatch	DOID:0111369	hyperalphalipoproteinemia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0007747	isolated hyperchlorhidrosis	skos:exactMatch	DOID:0111371	isolated hyperchlorhidrosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007758	epidermolytic palmoplantar keratoderma, 1	skos:exactMatch	DOID:0080223	epidermolytic palmoplantar keratoderma	semapv:ManualMappingCuration	2023-03-17
MONDO:0007762	hyperlipoproteinemia type V	skos:exactMatch	DOID:0111421	familial apolipoprotein A5 deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0007762	hyperlipoproteinemia type V	skos:exactMatch	DOID:1171	hyperlipoproteinemia type V	semapv:ManualMappingCuration	2023-03-17
MONDO:0007763	nonpapillary renal cell carcinoma	skos:exactMatch	DOID:0050387	nonpapillary renal cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0007764	autosomal dominant osteosclerosis, Worth type	skos:exactMatch	DOID:0080037	Worth syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007771	hyperpigmentation with or without hypopigmentation, familial progressive	skos:exactMatch	DOID:0111373	familial progressive hyperpigmentation with or without hypopigmentation	semapv:ManualMappingCuration	2023-03-17
MONDO:0007784	selective pituitary resistance to thyroid hormone	skos:exactMatch	DOID:0111374	selective pituitary thyroid hormone resistance	semapv:ManualMappingCuration	2023-03-17
MONDO:0007787	Ambras type hypertrichosis universalis congenita	skos:exactMatch	DOID:0111060	Ambras type hypertrichosis universalis congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0007790	Charcot-Marie-Tooth disease type 3	skos:exactMatch	DOID:0050540	Charcot-Marie-Tooth disease type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0007791	familial hypocalciuric hypercalcemia 1	skos:exactMatch	DOID:0060700	familial hypocalciuric hypercalcemia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007792	familial hypocalciuric hypercalcemia 2	skos:exactMatch	DOID:0060701	familial hypocalciuric hypercalcemia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007793	hypochondroplasia	skos:exactMatch	DOID:0080041	hypochondroplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007797	hypoparathyroidism-deafness-renal disease syndrome	skos:exactMatch	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007800	chromosome 18p deletion syndrome	skos:exactMatch	DOID:0060406	chromosome 18p deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007804	Pallister-Hall syndrome	skos:exactMatch	DOID:9248	Pallister-Hall syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007805	hypotrichosis 2	skos:exactMatch	DOID:0110699	hypotrichosis 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0007810	autosomal dominant ichthyosis vulgaris	skos:exactMatch	DOID:1702	ichthyosis vulgaris	semapv:ManualMappingCuration	2023-11-19
MONDO:0007813	superficial epidermolytic ichthyosis	skos:exactMatch	DOID:0060877	bullous congenital ichthyosiform erythroderma	semapv:ManualMappingCuration	2023-03-17
MONDO:0007818	hyper-IgE recurrent infection syndrome 1, autosomal dominant	skos:exactMatch	DOID:3261	hyper IgE recurrent infection syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007828	indifference to pain, congenital, autosomal dominant	skos:exactMatch	DOID:0081075	Marsili syndrome	semapv:ManualMappingCuration	2024-02-18
MONDO:0007836	IVIC syndrome	skos:exactMatch	DOID:0111381	IVIC syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007838	Jacobsen syndrome	skos:exactMatch	DOID:0111723	Jacobsen Syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007841	coxopodopatellar syndrome	skos:exactMatch	DOID:0111382	ischiocoxopodopatellar syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007844	hypogonadotropic hypogonadism 2 with or without anosmia	skos:exactMatch	DOID:0090083	hypogonadotropic hypogonadism 2 with or without anosmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007846	KBG syndrome	skos:exactMatch	DOID:14780	KBG syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007848	autosomal dominant keratitis	skos:exactMatch	DOID:0111383	autosomal dominant keratitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007850	autosomal dominant keratitis-ichthyosis-hearing loss syndrome	skos:exactMatch	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0007852	palmoplantar keratoderma-deafness syndrome	skos:exactMatch	DOID:0111505	palmoplantar keratoderma-deafness syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007856	palmoplantar keratoderma-esophageal carcinoma syndrome	skos:exactMatch	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007859	palmoplantar keratoderma i, striate, focal, or diffuse	skos:exactMatch	DOID:0081108	keratosis palmoplantaris striata 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0007862	Waardenburg syndrome type 3	skos:exactMatch	DOID:0110949	Waardenburg syndrome type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0007864	angioosteohypertrophic syndrome	skos:exactMatch	DOID:2926	Klippel-Trenaunay syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007866	Bart-Pumphrey syndrome	skos:exactMatch	DOID:0050658	Bart-Pumphrey syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007872	LADD syndrome	skos:exactMatch	DOID:0050331	lacrimoauriculodentodigital syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0007872	LADD syndrome	skos:exactMatch	DOID:0081370	LADD syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0007874	trichorhinophalangeal syndrome type II	skos:exactMatch	DOID:4998	trichorhinophalangeal syndrome type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0007875	Larsen syndrome	skos:exactMatch	DOID:14764	Larsen syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007878	congenital laryngomalacia	skos:exactMatch	DOID:0080833	laryngomalacia	semapv:ManualMappingCuration	2023-04-17
MONDO:0007885	Legg-Calve-Perthes disease	skos:exactMatch	DOID:14415	Legg-Calve-Perthes disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0007892	Lenz-Majewski hyperostotic dwarfism	skos:exactMatch	DOID:0111507	Lenz-Majewski hyperostotic dwarfism	semapv:ManualMappingCuration	2023-03-17
MONDO:0007893	Noonan syndrome with multiple lentigines	skos:exactMatch	DOID:14291	Noonan syndrome with multiple lentigines	semapv:ManualMappingCuration	2023-03-17
MONDO:0007895	platyspondylic dysplasia, Torrance type	skos:exactMatch	DOID:0111508	Torrance type platyspondylic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007900	nonsyndromic congenital nail disorder 3	skos:exactMatch	DOID:0080081	nonsyndromic congenital nail disorder 3	semapv:ManualMappingCuration	2023-11-19
MONDO:0007906	familial partial lipodystrophy, Dunnigan type	skos:exactMatch	DOID:0070202	familial partial lipodystrophy type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007909	familial multiple lipomatosis	skos:exactMatch	DOID:0070518	familial multiple lipomatosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0007915	systemic lupus erythematosus	skos:exactMatch	DOID:9074	systemic lupus erythematosus	semapv:ManualMappingCuration	2023-03-17
MONDO:0007918	microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability	skos:exactMatch	DOID:0060349	microcephaly with or without chorioretinopathy, lymphedema, or mental retardation	semapv:ManualMappingCuration	2023-03-17
MONDO:0007920	lymphatic malformation 5	skos:exactMatch	DOID:0070213	hereditary lymphedema II	semapv:ManualMappingCuration	2023-03-17
MONDO:0007922	lymphedema-distichiasis syndrome	skos:exactMatch	DOID:0111509	lymphedema-distichiasis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007924	Bannayan-Riley-Ruvalcaba syndrome	skos:exactMatch	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007925	myelodysplastic syndrome associated with isolated del(5q)	skos:exactMatch	DOID:0090016	chromosome 5q deletion syndrome	semapv:ManualMappingCuration	2024-06-23
MONDO:0007935	cystoid macular edema	skos:exactMatch	DOID:4447	cystoid macular edema	semapv:ManualMappingCuration	2023-03-17
MONDO:0007937	renal hypomagnesemia 2	skos:exactMatch	DOID:0060885	renal hypomagnesemia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0007938	46,XY sex reversal 4	skos:exactMatch	DOID:0111771	46,XY sex reversal 4	semapv:ManualMappingCuration	2023-11-19
MONDO:0007943	Nager acrofacial dysostosis	skos:exactMatch	DOID:5768	Nager acrofacial dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007946	jaw-winking syndrome	skos:exactMatch	DOID:560	jaw-winking syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007947	Marfan syndrome	skos:exactMatch	DOID:14323	Marfan syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007949	Marshall syndrome	skos:exactMatch	DOID:0111510	Marshall syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007953	Binder syndrome	skos:exactMatch	DOID:14683	Binder syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007958	familial medullary thyroid carcinoma	skos:exactMatch	DOID:0050547	familial medullary thyroid carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0007964	melanoma, cutaneous malignant, susceptibility to, 2	skos:exactMatch	DOID:10041	dysplastic nevus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007970	melorheostosis	skos:exactMatch	DOID:4253	melorheostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007979	metachondromatosis	skos:exactMatch	DOID:0111512	metachondromatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0007982	metaphyseal chondrodysplasia, Jansen type	skos:exactMatch	DOID:0080020	Jansen's metaphyseal chondrodysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007983	Schmid metaphyseal chondrodysplasia	skos:exactMatch	DOID:0080021	Schmid metaphyseal chondrodysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007984	metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome	skos:exactMatch	DOID:0111513	metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0007986	metatropic dysplasia	skos:exactMatch	DOID:0111514	metatropic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007987	Kniest dysplasia	skos:exactMatch	DOID:0080045	Kniest dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0007988	autosomal dominant primary microcephaly	skos:exactMatch	DOID:14725	autosomal dominant microcephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0007990	multiple benign circumferential skin creases on limbs	skos:exactMatch	DOID:0112241	multiple benign circumferential skin creases on limbs	semapv:ManualMappingCuration	2023-03-17
MONDO:0008006	Mobius syndrome	skos:exactMatch	DOID:13501	Moebius syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008007	tooth ankylosis	skos:exactMatch	DOID:12661	tooth ankylosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008009	monilethrix	skos:exactMatch	DOID:0050472	monilethrix	semapv:ManualMappingCuration	2023-03-17
MONDO:0008013	chromosome 9p deletion syndrome	skos:exactMatch	DOID:0060732	chromosome 9p deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008016	trismus-pseudocamptodactyly syndrome	skos:exactMatch	DOID:0111603	distal arthrogryposis type 7	semapv:ManualMappingCuration	2023-04-17
MONDO:0008018	Muir-Torre syndrome	skos:exactMatch	DOID:0050465	Muir-Torre syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008019	mullerian aplasia and hyperandrogenism	skos:exactMatch	DOID:0111526	Mullerian aplasia and hyperandrogenism	semapv:ManualMappingCuration	2023-03-17
MONDO:0008025	neuronopathy, distal hereditary motor, type 2A	skos:exactMatch	DOID:0111208	distal hereditary motor neuronopathy type 2A	semapv:ManualMappingCuration	2024-04-21
MONDO:0008026	autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures	skos:exactMatch	DOID:0070351	spinal muscular atrophy with lower extremity predominant 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0008029	Bethlem myopathy	skos:exactMatch	DOID:0050663	Bethlem myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008031	facioscapulohumeral muscular dystrophy 2	skos:exactMatch	DOID:0111193	facioscapulohumeral muscular dystrophy 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0008040	transient myeloproliferative syndrome	skos:exactMatch	DOID:0060888	transient myeloproliferative syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0008045	spinal muscular atrophy-progressive myoclonic epilepsy syndrome	skos:exactMatch	DOID:0111527	spinal muscular atrophy with progressive myoclonic epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008047	episodic ataxia type 1	skos:exactMatch	DOID:0050989	episodic ataxia type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008048	autosomal dominant centronuclear myopathy	skos:exactMatch	DOID:0111217	autosomal dominant centronuclear myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008048	autosomal dominant centronuclear myopathy	skos:exactMatch	DOID:0111223	centronuclear myopathy 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0008050	MYH7-related skeletal myopathy	skos:exactMatch	DOID:0070197	distal myopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008051	tubular aggregate myopathy	skos:exactMatch	DOID:0080089	tubular aggregate myopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008056	myotonic dystrophy type 1	skos:exactMatch	DOID:11722	myotonic dystrophy type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008058	cylindrical spirals myopathy	skos:exactMatch	DOID:0080103	cylindrical spirals myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008059	Naegeli-Franceschetti-Jadassohn syndrome	skos:exactMatch	DOID:0111528	Naegeli-Franceschetti-Jadassohn syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008060	nonsyndromic congenital nail disorder 1	skos:exactMatch	DOID:0080079	nonsyndromic congenital nail disorder 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008061	nail-patella syndrome	skos:exactMatch	DOID:9467	nail-patella syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008070	nemaline myopathy 3	skos:exactMatch	DOID:0110927	nemaline myopathy 3	semapv:ManualMappingCuration	2023-11-19
MONDO:0008075	schwannomatosis	skos:exactMatch	DOID:3204	schwannomatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008082	multiple endocrine neoplasia type 2B	skos:exactMatch	DOID:10016	multiple endocrine neoplasia type 2B	semapv:ManualMappingCuration	2023-03-17
MONDO:0008083	ceroid lipofuscinosis, neuronal, 4 (Kufs type)	skos:exactMatch	DOID:0110720	neuronal ceroid lipofuscinosis 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0008087	hereditary neuropathy with liability to pressure palsies	skos:exactMatch	DOID:0060843	hereditary neuropathy with liability to pressure palsies	semapv:ManualMappingCuration	2023-03-17
MONDO:0008090	cyclic hematopoiesis	skos:exactMatch	DOID:5339	cyclic hematopoiesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008092	hereditary neutrophilia	skos:exactMatch	DOID:0090120	hereditary neutrophilia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008093	nevus, epidermal	skos:exactMatch	DOID:0111162	epidermal nevus	semapv:ManualMappingCuration	2023-03-17
MONDO:0008094	familial multiple nevi flammei	skos:exactMatch	DOID:0111529	familial multiple nevi flammei	semapv:ManualMappingCuration	2023-03-17
MONDO:0008097	linear nevus sebaceous syndrome	skos:exactMatch	DOID:0111530	linear nevus sebaceous syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008111	oculodentodigital dysplasia	skos:exactMatch	DOID:0060291	oculodentodigital dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008116	oculopharyngeal muscular dystrophy	skos:exactMatch	DOID:11719	oculopharyngeal muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008119	spinocerebellar ataxia type 1	skos:exactMatch	DOID:0050954	spinocerebellar ataxia type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008123	autosomal dominant omodysplasia	skos:exactMatch	DOID:0080845	omodysplasia 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0008133	optic atrophy 3	skos:exactMatch	DOID:0111433	optic atrophy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0008134	autosomal dominant optic atrophy, classic form	skos:exactMatch	DOID:0111441	optic atrophy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008136	isolated optic nerve hypoplasia	skos:exactMatch	DOID:0111531	bilateral optic nerve hypoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008137	orofaciodigital syndrome X	skos:exactMatch	DOID:0060380	orofaciodigital syndrome X	semapv:ManualMappingCuration	2023-03-17
MONDO:0008145	Ollier disease	skos:exactMatch	DOID:4624	Ollier disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008146	osteogenesis imperfecta type 1	skos:exactMatch	DOID:0110334	osteogenesis imperfecta type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008147	osteogenesis imperfecta type 2	skos:exactMatch	DOID:0110341	osteogenesis imperfecta type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008148	osteogenesis imperfecta type 4	skos:exactMatch	DOID:0110340	osteogenesis imperfecta type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0008150	osteoglophonic dwarfism	skos:exactMatch	DOID:0111532	osteoglophonic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008151	gnathodiaphyseal dysplasia	skos:exactMatch	DOID:0111533	gnathodiaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008152	multicentric carpo-tarsal osteolysis with or without nephropathy	skos:exactMatch	DOID:0111534	multicentric carpotarsal osteolysis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008153	progressive osseous heteroplasia	skos:exactMatch	DOID:0111535	progressive osseous heteroplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008156	autosomal dominant osteopetrosis 2	skos:exactMatch	DOID:0110938	autosomal dominant osteopetrosis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008157	Buschke-Ollendorff syndrome	skos:exactMatch	DOID:0111536	Buschke-Ollendorff syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008170	ovarian cancer	skos:exactMatch	DOID:2394	ovarian cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0008178	inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1	skos:exactMatch	DOID:0111385	inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008179	paroxysmal extreme pain disorder	skos:exactMatch	DOID:0111537	paroxysmal extreme pain disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0008183	annular pancreas	skos:exactMatch	DOID:0060850	annular pancreas	semapv:ManualMappingCuration	2023-03-17
MONDO:0008195	paramyotonia congenita of Von Eulenburg	skos:exactMatch	DOID:0111538	paramyotonia congenita of Von Eulenburg	semapv:ManualMappingCuration	2023-03-17
MONDO:0008196	parastremmatic dwarfism	skos:exactMatch	DOID:0111539	parastremmatic dwarfism	semapv:ManualMappingCuration	2023-03-17
MONDO:0008199	late-onset Parkinson disease	skos:exactMatch	DOID:0060892	late onset Parkinson's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008201	Perry syndrome	skos:exactMatch	DOID:0060486	Perry syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008207	chondromalacia patellae	skos:exactMatch	DOID:13357	chondromalacia patellae	semapv:ManualMappingCuration	2023-03-17
MONDO:0008209	Char syndrome	skos:exactMatch	DOID:0060563	Char syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008210	patterned macular dystrophy 1	skos:exactMatch	DOID:0060866	patterned macular dystrophy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008215	adult-onset autosomal dominant demyelinating leukodystrophy	skos:exactMatch	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008218	Hailey-Hailey disease	skos:exactMatch	DOID:0050429	Hailey-Hailey disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008221	prolidase deficiency	skos:exactMatch	DOID:0111540	prolidase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008222	Andersen-Tawil syndrome	skos:exactMatch	DOID:0050434	Andersen-Tawil syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008223	hypokalemic periodic paralysis	skos:exactMatch	DOID:14452	hypokalemic periodic paralysis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008224	hyperkalemic periodic paralysis	skos:exactMatch	DOID:14451	hyperkalemic periodic paralysis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008231	Peyronie disease	skos:exactMatch	DOID:8616	Peyronie's disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0008233	pheochromocytoma	skos:exactMatch	DOID:0050771	pheochromocytoma	semapv:ManualMappingCuration	2024-08-18
MONDO:0008234	multiple endocrine neoplasia type 2A	skos:exactMatch	DOID:0050430	multiple endocrine neoplasia type 2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0008244	piebaldism	skos:exactMatch	DOID:3263	piebaldism	semapv:ManualMappingCuration	2023-03-17
MONDO:0008246	pigmented paravenous retinochoroidal atrophy	skos:exactMatch	DOID:0111541	pigmented paravenous chorioretinal atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008250	isolated growth hormone deficiency type II	skos:exactMatch	DOID:0060872	isolated growth hormone deficiency type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0008259	familial spontaneous pneumothorax	skos:exactMatch	DOID:0080218	primary spontaneous pneumothorax	semapv:ManualMappingCuration	2023-03-17
MONDO:0008260	Kindler syndrome	skos:exactMatch	DOID:0060472	Kindler syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008262	Poland syndrome	skos:exactMatch	DOID:12961	Poland syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008267	orofaciodigital syndrome V	skos:exactMatch	DOID:0060375	orofaciodigital syndrome V	semapv:ManualMappingCuration	2023-03-17
MONDO:0008275	familial expansile osteolysis	skos:exactMatch	DOID:0111542	familial expansile osteolysis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008276	generalized juvenile polyposis/juvenile polyposis coli	skos:exactMatch	DOID:0050787	juvenile polyposis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008278	juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome	skos:exactMatch	DOID:0111543	juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008280	Peutz-Jeghers syndrome	skos:exactMatch	DOID:3852	Peutz-Jeghers syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008283	Cronkhite-Canada syndrome	skos:exactMatch	DOID:6225	Cronkhite-Canada syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008287	Greig cephalopolysyndactyly syndrome	skos:exactMatch	DOID:14761	Greig cephalopolysyndactyly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008289	brain small vessel disease 1 with or without ocular anomalies	skos:exactMatch	DOID:0090125	brain small vessel disease 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008292	punctate palmoplantar keratoderma type 2	skos:exactMatch	DOID:0080213	punctate palmoplantar keratoderma type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0008294	acute intermittent porphyria	skos:exactMatch	DOID:3890	acute intermittent porphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0008297	variegate porphyria	skos:exactMatch	DOID:4346	variegate porphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0008300	Prader-Willi syndrome	skos:exactMatch	DOID:11983	Prader-Willi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008301	Guttmacher syndrome	skos:exactMatch	DOID:0111544	Guttmacher syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008303	familial male-limited precocious puberty	skos:exactMatch	DOID:0111545	familial male-limited precocious puberty	semapv:ManualMappingCuration	2024-04-21
MONDO:0008305	Currarino triad	skos:exactMatch	DOID:0111546	Currarino syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008306	ABri amyloidosis	skos:exactMatch	DOID:0070029	ITM2B-related cerebral amyloid angiopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008310	Hutchinson-Gilford progeria syndrome	skos:exactMatch	DOID:3911	progeria	semapv:ManualMappingCuration	2023-03-17
MONDO:0008315	prostate cancer	skos:exactMatch	DOID:10283	prostate cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0008318	Proteus syndrome	skos:exactMatch	DOID:13482	Proteus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008322	pseudoachondroplasia	skos:exactMatch	DOID:0080047	pseudoachondroplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008323	Liddle syndrome	skos:exactMatch	DOID:0050477	Liddle syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008329	autosomal dominant pseudohypoaldosteronism type 1	skos:exactMatch	DOID:0060855	autosomal dominant pseudohypoaldosteronism type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008332	platelet-type von Willebrand disease	skos:exactMatch	DOID:0111056	platelet-type bleeding disorder 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0008338	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A	skos:exactMatch	DOID:0081321	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A	semapv:ManualMappingCuration	2023-04-17
MONDO:0008340	ptosis, hereditary congenital, 1	skos:exactMatch	DOID:0060261	congenital ptosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008371	Dowling-Degos disease	skos:exactMatch	DOID:0060256	Dowling-Degos disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008373	retinal arterial tortuosity	skos:exactMatch	DOID:0111547	retinal arterial tortuosity	semapv:ManualMappingCuration	2023-03-17
MONDO:0008380	retinoblastoma	skos:exactMatch	DOID:768	retinoblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0008386	Axenfeld-Rieger syndrome type 1	skos:exactMatch	DOID:0110120	Axenfeld-Rieger syndrome type 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0008387	ring dermoid of cornea	skos:exactMatch	DOID:0111548	ring dermoid of cornea	semapv:ManualMappingCuration	2023-03-17
MONDO:0008394	Silver-Russell syndrome	skos:exactMatch	DOID:14681	Silver-Russell syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008397	aplasia of lacrimal and salivary glands	skos:exactMatch	DOID:0111549	aplasia of lacrimal and salivary glands	semapv:ManualMappingCuration	2023-03-17
MONDO:0008404	scalp-ear-nipple syndrome	skos:exactMatch	DOID:0111550	scalp-ear-nipple syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008407	neurogenic scapuloperoneal syndrome, Kaeser type	skos:exactMatch	DOID:0111551	neurogenic scapuloperoneal syndrome Kaeser type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008409	congenital myopathy 7A, myosin storage, autosomal dominant	skos:exactMatch	DOID:0111269	autosomal dominant hyaline body myopathy	semapv:ManualMappingCuration	2023-08-20
MONDO:0008410	Scheuermann disease	skos:exactMatch	DOID:13300	Scheuermann's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008411	ulnar-mammary syndrome	skos:exactMatch	DOID:0060614	ulnar-mammary syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008412	intestinal schistosomiasis	skos:exactMatch	DOID:0050597	intestinal schistosomiasis	semapv:ManualMappingCuration	2024-04-21
MONDO:0008422	autosomal dominant sideroblastic anemia	skos:exactMatch	DOID:0060335	autosomal dominant sideroblastic anemia 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0008428	septooptic dysplasia	skos:exactMatch	DOID:0060857	septooptic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008434	Smith-Magenis syndrome	skos:exactMatch	DOID:0060768	Smith-Magenis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008437	hereditary spastic paraplegia 3A	skos:exactMatch	DOID:0110791	hereditary spastic paraplegia 3A	semapv:ManualMappingCuration	2023-03-17
MONDO:0008438	hereditary spastic paraplegia 4	skos:exactMatch	DOID:0110792	hereditary spastic paraplegia 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0008451	neuronopathy, distal hereditary motor, autosomal dominant 1	skos:exactMatch	DOID:0111200	autosomal dominant distal hereditary motor neuronopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008453	adult-onset proximal spinal muscular atrophy, autosomal dominant	skos:exactMatch	DOID:0111194	autosomal dominant adult-onset proximal spinal muscular atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008457	spinocerebellar ataxia type 6	skos:exactMatch	DOID:0050956	spinocerebellar ataxia type 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0008458	spinocerebellar ataxia type 2	skos:exactMatch	DOID:0050955	spinocerebellar ataxia type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008458	spinocerebellar ataxia type 2	skos:exactMatch	DOID:0060204	amyotrophic lateral sclerosis type 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0008471	spondyloepiphyseal dysplasia congenita	skos:exactMatch	DOID:14789	spondyloepiphyseal dysplasia congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0008473	spondyloepimetaphyseal dysplasia, Maroteaux type	skos:exactMatch	DOID:0111553	spondyloepiphyseal dysplasia Maroteaux type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008474	spondyloepiphyseal dysplasia tarda, autosomal dominant	skos:exactMatch	DOID:0112285	autosomal dominant spondyloepiphyseal dysplasia tarda	semapv:ManualMappingCuration	2024-04-21
MONDO:0008476	spondyloepimetaphyseal dysplasia, Strudwick type	skos:exactMatch	DOID:0080028	spondyloepimetaphyseal dysplasia, Strudwick type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008477	spondylometaphyseal dysplasia, Kozlowski type	skos:exactMatch	DOID:0111554	spondylometaphyseal dysplasia Kozlowski type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008478	spondylometaphyseal dysplasia, Schmidt type	skos:exactMatch	DOID:0112296	spondylometaphyseal dysplasia Algerian type	semapv:ManualMappingCuration	2023-04-17
MONDO:0008479	spondylometaphyseal dysplasia, 'corner fracture' type	skos:exactMatch	DOID:0112297	spondylometaphyseal dysplasia corner fracture type	semapv:ManualMappingCuration	2023-06-18
MONDO:0008485	sebocystomatosis	skos:exactMatch	DOID:0111556	steatocystoma multiplex	semapv:ManualMappingCuration	2023-03-17
MONDO:0008490	otospondylomegaepiphyseal dysplasia, autosomal dominant	skos:exactMatch	DOID:0080677	otospondylomegaepiphyseal dysplasia, autosomal dominant	semapv:ManualMappingCuration	2023-03-17
MONDO:0008490	otospondylomegaepiphyseal dysplasia, autosomal dominant	skos:exactMatch	DOID:4258	Weissenbacher-Zweymuller syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008492	stiff skin syndrome	skos:exactMatch	DOID:0111561	stiff skin syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008493	overhydrated hereditary stomatocytosis	skos:exactMatch	DOID:0111562	overhydrated hereditary stomatocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008497	Stormorken syndrome	skos:exactMatch	DOID:0060354	Stormorken syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008501	Sturge-Weber syndrome	skos:exactMatch	DOID:0111563	Sturge-Weber syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008504	supravalvular aortic stenosis	skos:exactMatch	DOID:1929	supravalvular aortic stenosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008511	proximal symphalangism	skos:exactMatch	DOID:0050788	proximal symphalangism	semapv:ManualMappingCuration	2023-03-17
MONDO:0008512	syndactyly type 1	skos:exactMatch	DOID:0111816	syndactyly type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008514	syndactyly type 3	skos:exactMatch	DOID:0111817	syndactyly type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0008515	syndactyly type 4	skos:exactMatch	DOID:0111818	syndactyly type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0008516	syndactyly type 5	skos:exactMatch	DOID:0111819	syndactyly type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0008519	multiple synostoses syndrome 1	skos:exactMatch	DOID:0081317	multiple synostoses syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0008521	tarsal-carpal coalition syndrome	skos:exactMatch	DOID:0050789	tarsal-carpal coalition syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008523	Blau syndrome	skos:exactMatch	DOID:0050678	Blau syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008553	platelet-type bleeding disorder 17	skos:exactMatch	DOID:0111049	platelet-type bleeding disorder 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0008559	thrombophilia due to thrombin defect	skos:exactMatch	DOID:0080701	prothrombin thrombophilia	semapv:ManualMappingCuration	2023-04-17
MONDO:0008559	thrombophilia due to thrombin defect	skos:exactMatch	DOID:0111907	thrombophilia due to thrombin defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0008560	thrombophilia due to activated protein C resistance	skos:exactMatch	DOID:0111902	thrombophilia due to activated protein C resistance	semapv:ManualMappingCuration	2023-03-17
MONDO:0008572	tibia, hypoplasia or aplasia of, with polydactyly	skos:exactMatch	DOID:0111564	hypoplastic or aplastic tibia with polydactyly	semapv:ManualMappingCuration	2023-11-19
MONDO:0008582	tooth and nail syndrome	skos:exactMatch	DOID:6678	tooth and nail syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008592	tricho-dento-osseous syndrome	skos:exactMatch	DOID:0111565	trichodontoosseous syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008597	trichorhinophalangeal syndrome, type III	skos:exactMatch	DOID:0080376	trichorhinophalangeal syndrome type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0008610	blue color blindness	skos:exactMatch	DOID:11661	blue color blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0008627	ureter cancer	skos:exactMatch	DOID:11819	ureter cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0008633	Muckle-Wells syndrome	skos:exactMatch	DOID:0050854	Muckle-Wells syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008638	varicose disease	skos:exactMatch	DOID:799	varicose veins	semapv:ManualMappingCuration	2023-03-17
MONDO:0008641	retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations	skos:exactMatch	DOID:0111567	retinal vasculopathy with cerebral leukodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008642	VACTERL/vater association	skos:exactMatch	DOID:14679	VACTERL association	semapv:ManualMappingCuration	2023-03-17
MONDO:0008647	hypertrophic cardiomyopathy 1	skos:exactMatch	DOID:0110307	hypertrophic cardiomyopathy 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0008652	congenital vertical talus	skos:exactMatch	DOID:0111568	congenital vertical talus	semapv:ManualMappingCuration	2023-03-17
MONDO:0008660	autosomal dominant hypophosphatemic rickets	skos:exactMatch	DOID:0050948	autosomal dominant hypophosphatemic rickets	semapv:ManualMappingCuration	2023-03-17
MONDO:0008662	autosomal dominant vitreoretinochoroidopathy	skos:exactMatch	DOID:0111569	autosomal dominant vitreoretinochoroidopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008663	snowflake vitreoretinal degeneration	skos:exactMatch	DOID:0111570	snowflake vitreoretinal degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0008667	von Hippel-Lindau disease	skos:exactMatch	DOID:14175	von Hippel-Lindau disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008668	von Willebrand disease 1	skos:exactMatch	DOID:0060573	von Willebrand's disease 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008670	Waardenburg syndrome type 1	skos:exactMatch	DOID:0110948	Waardenburg syndrome type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008671	Waardenburg syndrome type 2A	skos:exactMatch	DOID:0110950	Waardenburg syndrome type 2A	semapv:ManualMappingCuration	2024-04-21
MONDO:0008672	Watson syndrome	skos:exactMatch	DOID:0070483	Watson syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0008673	acrofacial dysostosis, Weyers type	skos:exactMatch	DOID:0111571	Weyers acrofacial dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008676	white sponge nevus 1	skos:exactMatch	DOID:0081287	white sponge nevus 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0008678	Williams syndrome	skos:exactMatch	DOID:1928	Williams-Beuren syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008681	WAGR syndrome	skos:exactMatch	DOID:14515	WAGR syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008682	Denys-Drash syndrome	skos:exactMatch	DOID:3764	Denys-Drash syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008684	Wolf-Hirschhorn syndrome	skos:exactMatch	DOID:0050460	Wolf-Hirschhorn syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008686	isolated familial wooly hair disorder	skos:exactMatch	DOID:0111572	familial woolly hair syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008689	dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema	skos:exactMatch	DOID:0111576	dehydrated hereditary stomatocytosis 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0008692	abetalipoproteinemia	skos:exactMatch	DOID:1386	abetalipoproteinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008693	ablepharon macrostomia syndrome	skos:exactMatch	DOID:0060550	ablepharon macrostomia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008695	chorea-acanthocytosis	skos:exactMatch	DOID:0050766	choreaacanthocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008699	achalasia microcephaly syndrome	skos:exactMatch	DOID:0050796	achalasia microcephaly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008700	acheiropody	skos:exactMatch	DOID:0050603	acheiropody	semapv:ManualMappingCuration	2023-03-17
MONDO:0008701	achondrogenesis type IA	skos:exactMatch	DOID:0080054	achondrogenesis type IA	semapv:ManualMappingCuration	2023-03-17
MONDO:0008702	achondrogenesis type II	skos:exactMatch	DOID:0080056	achondrogenesis type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0008703	acromesomelic dysplasia 2A	skos:exactMatch	DOID:0080052	acromesomelic dysplasia, Grebe type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008708	acrocallosal syndrome	skos:exactMatch	DOID:9250	acrocallosal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008713	acrodermatitis enteropathica	skos:exactMatch	DOID:0050605	acrodermatitis enteropathica	semapv:ManualMappingCuration	2023-03-17
MONDO:0008714	acrofacial dysostosis Rodriguez type	skos:exactMatch	DOID:0060383	acrofacial dysostosis Rodriguez type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008715	acrofrontofacionasal dysostosis	skos:exactMatch	DOID:0060226	acrofrontofacionasal dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008717	acromesomelic dysplasia 2C, Hunter-Thompson type	skos:exactMatch	DOID:0080051	acromesomelic dysplasia, Hunter-Thompson type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008721	medium chain acyl-CoA dehydrogenase deficiency	skos:exactMatch	DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008722	short chain acyl-CoA dehydrogenase deficiency	skos:exactMatch	DOID:0080154	short chain acyl-CoA dehydrogenase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008723	very long chain acyl-CoA dehydrogenase deficiency	skos:exactMatch	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008733	familial glucocorticoid deficiency	skos:exactMatch	DOID:0080620	familial glucocorticoid deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008737	congenital afibrinogenemia	skos:exactMatch	DOID:2236	congenital afibrinogenemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008740	agnathia-otocephaly complex	skos:exactMatch	DOID:0060341	agnathia-otocephaly complex	semapv:ManualMappingCuration	2023-03-17
MONDO:0008742	autosomal dominant severe congenital neutropenia	skos:exactMatch	DOID:0112130	autosomal dominant severe congenital neutropenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008745	oculocutaneous albinism type 1A	skos:exactMatch	DOID:0070094	oculocutaneous albinism type IA	semapv:ManualMappingCuration	2023-03-17
MONDO:0008746	oculocutaneous albinism type 2	skos:exactMatch	DOID:0070096	oculocutaneous albinism type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0008747	oculocutaneous albinism type 3	skos:exactMatch	DOID:0070097	oculocutaneous albinism type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0008752	Alexander disease	skos:exactMatch	DOID:4252	Alexander disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008753	alkaptonuria	skos:exactMatch	DOID:9270	alkaptonuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0008756	alopecia - intellectual disability syndrome	skos:exactMatch	DOID:0080627	alopecia-mental retardation syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008757	alopecia universalis congenita	skos:exactMatch	DOID:0050634	alopecia universalis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008758	mitochondrial DNA depletion syndrome 4a	skos:exactMatch	DOID:0080122	Alpers-Huttenlocher syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008759	oxoglutaricaciduria	skos:exactMatch	DOID:0081326	oxoglutarate dehydrogenase deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0008760	beta-ketothiolase deficiency	skos:exactMatch	DOID:14723	beta-ketothiolase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008762	autosomal recessive Alport syndrome	skos:exactMatch	DOID:0110033	autosomal recessive Alport syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008763	Alstrom syndrome	skos:exactMatch	DOID:0050473	Alstrom syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008764	Leber congenital amaurosis 1	skos:exactMatch	DOID:0110078	Leber congenital amaurosis 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0008765	Leber congenital amaurosis 2	skos:exactMatch	DOID:0110016	Leber congenital amaurosis 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0008767	neuronal ceroid lipofuscinosis 3	skos:exactMatch	DOID:0110731	neuronal ceroid lipofuscinosis 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0008768	ceroid lipofuscinosis, neuronal, 6B (Kufs type)	skos:exactMatch	DOID:0110730	neuronal ceroid lipofuscinosis 6B	semapv:ManualMappingCuration	2023-03-17
MONDO:0008769	neuronal ceroid lipofuscinosis 2	skos:exactMatch	DOID:0110726	neuronal ceroid lipofuscinosis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008771	amelogenesis imperfecta type 1G	skos:exactMatch	DOID:0110066	amelogenesis imperfecta type 1G	semapv:ManualMappingCuration	2023-03-17
MONDO:0008774	2-aminoadipic 2-oxoadipic aciduria	skos:exactMatch	DOID:0111453	2-aminoadipic 2-oxoadipic aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0008777	gelatinous drop-like corneal dystrophy	skos:exactMatch	DOID:0060449	gelatinous drop-like corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008780	amyotrophic lateral sclerosis type 2, juvenile	skos:exactMatch	DOID:0060194	juvenile amyotrophic lateral sclerosis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008783	Tangier disease	skos:exactMatch	DOID:1388	Tangier disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008795	aniridia-cerebellar ataxia-intellectual disability syndrome	skos:exactMatch	DOID:0111578	Gillespie syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008797	anodontia	skos:exactMatch	DOID:13714	anodontia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008798	nonsyndromic congenital nail disorder 4	skos:exactMatch	DOID:0080082	nonsyndromic congenital nail disorder 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0008799	anophthalmia/microphthalmia-esophageal atresia syndrome	skos:exactMatch	DOID:0111801	syndromic microphthalmia 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0008800	microphthalmia with limb anomalies	skos:exactMatch	DOID:0060861	microphthalmia with limb anomalies	semapv:ManualMappingCuration	2023-03-17
MONDO:0008803	Antley-Bixler syndrome	skos:exactMatch	DOID:0050462	Antley-Bixler syndrome with disordered steroidogenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008803	Antley-Bixler syndrome	skos:exactMatch	DOID:0081289	Antley-Bixler syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0008810	familial apolipoprotein C-II deficiency	skos:exactMatch	DOID:0111418	familial apolipoprotein C-II deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008814	hyperargininemia	skos:exactMatch	DOID:9278	hyperargininemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008815	argininosuccinic aciduria	skos:exactMatch	DOID:14755	argininosuccinic aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0008818	arterial tortuosity syndrome	skos:exactMatch	DOID:0050645	arterial tortuosity syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008823	arthrogryposis multiplex congenita 2, neurogenic type	skos:exactMatch	DOID:0090124	neurogenic-type arthrogryposis multiplex congenita-2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008824	fetal akinesia deformation sequence	skos:exactMatch	DOID:0111375	fetal akinesia deformation sequence syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008827	progressive pseudorheumatoid arthropathy of childhood	skos:exactMatch	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood	semapv:ManualMappingCuration	2023-03-17
MONDO:0008830	aspartylglucosaminuria	skos:exactMatch	DOID:0050461	aspartylglucosaminuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0008832	right atrial isomerism	skos:exactMatch	DOID:0060856	right atrial isomerism	semapv:ManualMappingCuration	2023-03-17
MONDO:0008834	asthma, nasal polyps, and aspirin intolerance	skos:exactMatch	DOID:0111579	asthma, nasal polyps, and aspirin intolerance	semapv:ManualMappingCuration	2023-11-19
MONDO:0008840	ataxia telangiectasia	skos:exactMatch	DOID:12704	ataxia telangiectasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008842	ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia	skos:exactMatch	DOID:0050754	ataxia with oculomotor apraxia type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008846	atransferrinemia	skos:exactMatch	DOID:0050649	atransferrinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008847	atrichia with papular lesions	skos:exactMatch	DOID:0060689	atrichia with papular lesions	semapv:ManualMappingCuration	2023-03-17
MONDO:0008849	atrophoderma vermiculata	skos:exactMatch	DOID:0080756	atrophoderma vermiculata	semapv:ManualMappingCuration	2023-03-17
MONDO:0008853	Barber-Say syndrome	skos:exactMatch	DOID:0060549	Barber-Say syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008855	MHC class II deficiency	skos:exactMatch	DOID:5812	MHC class II deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008856	immunodeficiency 27A	skos:exactMatch	DOID:0111955	immunodeficiency 27A	semapv:ManualMappingCuration	2023-03-17
MONDO:0008858	Behr syndrome	skos:exactMatch	DOID:0111580	Behr syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008862	3-methylcrotonyl-CoA carboxylase 2 deficiency	skos:exactMatch	DOID:0080580	3-methylcrotonyl-CoA carboxylase 2 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008863	sitosterolemia	skos:exactMatch	DOID:0090019	sitosterolemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008865	Bietti crystalline corneoretinal dystrophy	skos:exactMatch	DOID:0050664	Bietti crystalline corneoretinal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0008867	biliary atresia	skos:exactMatch	DOID:13608	biliary atresia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008869	Seckel syndrome 1	skos:exactMatch	DOID:0070007	Seckel syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008871	microcephalic osteodysplastic primordial dwarfism type I	skos:exactMatch	DOID:0060608	microcephalic osteodysplastic primordial dwarfism type I	semapv:ManualMappingCuration	2024-04-21
MONDO:0008872	microcephalic osteodysplastic primordial dwarfism type II	skos:exactMatch	DOID:0060609	microcephalic osteodysplastic primordial dwarfism type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0008876	Bloom syndrome	skos:exactMatch	DOID:2717	Bloom syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008879	Bowen-Conradi syndrome	skos:exactMatch	DOID:0050684	Bowen-Conradi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008885	Elsahy-Waters syndrome	skos:exactMatch	DOID:0080631	Elsahy-Waters syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008887	bronchiectasis with or without elevated sweat chloride 1	skos:exactMatch	DOID:0080526	bronchiectasis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008891	riboflavin transporter deficiency	skos:exactMatch	DOID:0050694	Brown-Vialetto-Van Laere syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008892	progressive familial intrahepatic cholestasis type 1	skos:exactMatch	DOID:0070226	progressive familial intrahepatic cholestasis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008893	C syndrome	skos:exactMatch	DOID:0111581	C syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008895	hereditary arterial and articular multiple calcification syndrome	skos:exactMatch	DOID:0111582	hereditary arterial and articular multiple calcification syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008903	lung cancer	skos:exactMatch	DOID:1324	lung cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0008907	PMM2-congenital disorder of glycosylation	skos:exactMatch	DOID:0080552	congenital disorder of glycosylation Ia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008908	MGAT2-congenital disorder of glycosylation	skos:exactMatch	DOID:0070253	congenital disorder of glycosylation type IIa	semapv:ManualMappingCuration	2023-03-17
MONDO:0008913	cardiac valvular defect, developmental	skos:exactMatch	DOID:0080633	developmental cardiac valvular defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0008915	dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome	skos:exactMatch	DOID:0111584	dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008918	carnitine-acylcarnitine translocase deficiency	skos:exactMatch	DOID:0111585	carnitine-acylcarnitine translocase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0008919	systemic primary carnitine deficiency disease	skos:exactMatch	DOID:14365	systemic primary carnitine deficiency disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0008922	Sengers syndrome	skos:exactMatch	DOID:0080132	Sengers syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008923	autosomal recessive palmoplantar keratoderma and congenital alopecia	skos:exactMatch	DOID:0111245	palmoplantar keratoderma and congenital alopecia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008925	cataract 46 juvenile-onset	skos:exactMatch	DOID:0110243	cataract 46 juvenile-onset	semapv:ManualMappingCuration	2023-03-17
MONDO:0008926	COFS syndrome	skos:exactMatch	DOID:0080910	cerebrooculofacioskeletal syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0008931	Cenani-Lenz syndactyly syndrome	skos:exactMatch	DOID:0090015	Cenani-Lenz syndactyly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008935	cerebellar ataxia-hypogonadism syndrome	skos:exactMatch	DOID:0111587	Gordon Holmes syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008939	isolated cerebellar hypoplasia/agenesis	skos:exactMatch	DOID:0070338	cerebellar hypoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008943	autosomal recessive spinocerebellar ataxia 2	skos:exactMatch	DOID:0080061	autosomal recessive spinocerebellar ataxia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0008944	Joubert syndrome 1	skos:exactMatch	DOID:0110980	Joubert syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0008947	bilateral striopallidodentate calcinosis	skos:exactMatch	DOID:0060230	basal ganglia calcification	semapv:ManualMappingCuration	2023-03-17
MONDO:0008948	cerebrotendinous xanthomatosis	skos:exactMatch	DOID:4810	cerebrotendinous xanthomatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0008953	peroxisome biogenesis disorder 1A (Zellweger)	skos:exactMatch	DOID:0080476	peroxisome biogenesis disorder 1A	semapv:ManualMappingCuration	2023-04-17
MONDO:0008954	peroxisome biogenesis disorder 2A (Zellweger)	skos:exactMatch	DOID:0080477	peroxisome biogenesis disorder 2A	semapv:ManualMappingCuration	2023-04-17
MONDO:0008955	cerebrooculofacioskeletal syndrome 1	skos:exactMatch	DOID:0080911	cerebrooculofacioskeletal syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0008958	Klippel-Feil syndrome 2, autosomal recessive	skos:exactMatch	DOID:0080590	Klippel-Feil syndrome 2	semapv:ManualMappingCuration	2024-02-18
MONDO:0008961	Charcot-Marie-Tooth disease type 4A	skos:exactMatch	DOID:0110185	Charcot-Marie-Tooth disease type 4A	semapv:ManualMappingCuration	2023-03-17
MONDO:0008962	Griscelli syndrome type 1	skos:exactMatch	DOID:0060832	Griscelli syndrome type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008963	Chediak-Higashi syndrome	skos:exactMatch	DOID:2935	Chediak-Higashi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008964	congenital secretory chloride diarrhea 1	skos:exactMatch	DOID:0060296	congenital secretory chloride diarrhea 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008965	CHARGE syndrome	skos:exactMatch	DOID:0050834	CHARGE syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008966	Aagenaes syndrome	skos:exactMatch	DOID:6691	Aagenaes syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008967	congenital bile acid synthesis defect 4	skos:exactMatch	DOID:0111068	congenital bile acid synthesis defect 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0008970	chondrodysplasia Blomstrand type	skos:exactMatch	DOID:0060387	chondrodysplasia Blomstrand type	semapv:ManualMappingCuration	2023-03-17
MONDO:0008972	rhizomelic chondrodysplasia punctata type 1	skos:exactMatch	DOID:0110851	rhizomelic chondrodysplasia punctata type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0008974	Greenberg dysplasia	skos:exactMatch	DOID:0111588	Greenberg dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008975	otospondylomegaepiphyseal dysplasia	skos:exactMatch	DOID:0080026	otospondylomegaepiphyseal dysplasia, autosomal recessive	semapv:ManualMappingCuration	2023-03-17
MONDO:0008978	chordoma	skos:exactMatch	DOID:3302	chordoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0008980	ataxia-hypogonadism-choroidal dystrophy syndrome	skos:exactMatch	DOID:0111265	Boucher-Neuhauser syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008988	citrullinemia type I	skos:exactMatch	DOID:0070340	classic citrullinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0008995	Yunis-Varon syndrome	skos:exactMatch	DOID:0060589	Yunis-Varon syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0008999	Cohen syndrome	skos:exactMatch	DOID:0111590	Cohen syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009007	Jalili syndrome	skos:exactMatch	DOID:0111404	Jalili syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009008	heart defect - tongue hamartoma - polysyndactyly syndrome	skos:exactMatch	DOID:0111591	congenital heart defects, hamartomas of tongue, and polysyndactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0009009	hypoplasminogenemia	skos:exactMatch	DOID:0111592	plasminogen deficiency type I	semapv:ManualMappingCuration	2023-04-17
MONDO:0009015	corneal dystrophy-perceptive deafness syndrome	skos:exactMatch	DOID:0111620	corneal dystrophy-perceptive deafness syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009019	congenital hereditary endothelial dystrophy of cornea	skos:exactMatch	DOID:0060649	congenital hereditary endothelial dystrophy of cornea	semapv:ManualMappingCuration	2023-03-17
MONDO:0009020	macular corneal dystrophy	skos:exactMatch	DOID:2565	macular corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009025	apparent mineralocorticoid excess	skos:exactMatch	DOID:4367	apparent mineralocorticoid excess syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009026	Costello syndrome	skos:exactMatch	DOID:0050469	Costello syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009031	craniodiaphyseal dysplasia	skos:exactMatch	DOID:0080032	craniodiaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009032	cranioectodermal dysplasia	skos:exactMatch	DOID:0050577	cranioectodermal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009033	temtamy syndrome	skos:exactMatch	DOID:0111621	Temtamy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009035	craniometaphyseal dysplasia, autosomal recessive	skos:exactMatch	DOID:0080802	autosomal recessive craniometaphyseal dysplasia	semapv:ManualMappingCuration	2024-04-21
MONDO:0009039	Baller-Gerold syndrome	skos:exactMatch	DOID:0050654	Baller-Gerold syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009044	Crigler-Najjar syndrome	skos:exactMatch	DOID:3803	Crigler-Najjar syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009046	Fraser syndrome	skos:exactMatch	DOID:0090001	Fraser syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009052	cutis laxa, autosomal recessive, type 1A	skos:exactMatch	DOID:0070135	autosomal recessive cutis laxa type IA	semapv:ManualMappingCuration	2024-04-21
MONDO:0009053	ALDH18A1-related de Barsy syndrome	skos:exactMatch	DOID:0070132	autosomal recessive cutis laxa type IIIA	semapv:ManualMappingCuration	2023-03-17
MONDO:0009054	autosomal recessive cutis laxa type 2, classic type	skos:exactMatch	DOID:0070141	autosomal recessive cutis laxa type II classic type	semapv:ManualMappingCuration	2023-03-17
MONDO:0009058	cystathioninuria	skos:exactMatch	DOID:0090142	cystathioninuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009061	cystic fibrosis	skos:exactMatch	DOID:1485	cystic fibrosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009063	ventriculomegaly-cystic kidney disease	skos:exactMatch	DOID:0111625	ventriculomegaly - cystic kidney disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009067	cystinuria	skos:exactMatch	DOID:9266	cystinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009068	cytochrome-c oxidase deficiency disease	skos:exactMatch	DOID:3762	cytochrome-c oxidase deficiency disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009069	congenital lactic acidosis, Saguenay-Lac-Saint-Jean type	skos:exactMatch	DOID:0111180	French Canadian Leigh disease	semapv:ManualMappingCuration	2023-06-18
MONDO:0009070	D-glyceric aciduria	skos:exactMatch	DOID:0111626	D-glyceric aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009073	Ritscher-Schinzel syndrome 1	skos:exactMatch	DOID:0060571	Ritscher-Schinzel syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0009079	DOORS syndrome	skos:exactMatch	DOID:0111627	DOORS syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009080	split hand-foot malformation 1 with sensorineural hearing loss	skos:exactMatch	DOID:0090024	split hand-foot malformation 1 with sensorineural hearing loss	semapv:ManualMappingCuration	2023-03-17
MONDO:0009082	high myopia-sensorineural deafness syndrome	skos:exactMatch	DOID:0111628	high myopia-sensorineural deafness syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009090	hearing loss, sensorineural, autosomal-mitochondrial type	skos:exactMatch	DOID:0111752	autosomal-mitochondrial sensorineural deafness	semapv:ManualMappingCuration	2024-02-18
MONDO:0009092	polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly	skos:exactMatch	DOID:0090112	Nasu-Hakola disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009104	Donnai-Barrow syndrome	skos:exactMatch	DOID:0090144	Donnai-Barrow syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009105	trichohepatoenteric syndrome	skos:exactMatch	DOID:0111414	trichohepatoenteric syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009107	diastrophic dysplasia	skos:exactMatch	DOID:14687	diastrophic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009109	lysinuric protein intolerance	skos:exactMatch	DOID:0060439	lysinuric protein intolerance	semapv:ManualMappingCuration	2023-03-17
MONDO:0009110	dicarboxylic aminoaciduria	skos:exactMatch	DOID:0060650	dicarboxylic aminoaciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009111	dihydropyrimidinuria	skos:exactMatch	DOID:0111629	dihydropyrimidinase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009112	rhizomelic chondrodysplasia punctata type 2	skos:exactMatch	DOID:0110852	rhizomelic chondrodysplasia punctata type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009113	hemolytic anemia due to diphosphoglycerate mutase deficiency	skos:exactMatch	DOID:0111630	familial erythrocytosis 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0009114	congenital sucrase-isomaltase deficiency	skos:exactMatch	DOID:0111633	congenital sucrase-isomaltase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009115	congenital lactase deficiency	skos:exactMatch	DOID:0111646	congenital lactase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009123	orthostatic hypotension 1	skos:exactMatch	DOID:0090145	dopamine beta-hydroxylase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009124	Dubowitz syndrome	skos:exactMatch	DOID:14796	Dubowitz syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009126	duodenal atresia	skos:exactMatch	DOID:0080216	duodenal atresia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009130	Dyggve-Melchior-Clausen disease	skos:exactMatch	DOID:0111167	Dyggve-Melchior-Clausen disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009131	Riley-Day syndrome	skos:exactMatch	DOID:11589	Riley-Day syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009133	cerebellar ataxia, intellectual disability, and dysequilibrium	skos:exactMatch	DOID:0050997	cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009134	congenital dyserythropoietic anemia type 2	skos:exactMatch	DOID:0111401	congenital dyserythropoietic anemia type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0009136	dyskeratosis congenita, autosomal recessive 1	skos:exactMatch	DOID:0070015	autosomal recessive dyskeratosis congenita 1	semapv:ManualMappingCuration	2024-08-18
MONDO:0009140	Silverman-Handmaker type dyssegmental dysplasia	skos:exactMatch	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009141	torsion dystonia 2	skos:exactMatch	DOID:0090038	torsion dystonia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009145	SchC6pf-Schulz-Passarge syndrome	skos:exactMatch	DOID:0111647	Schopf-Schulz-Passarge syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009151	cleft lip/palate-ectodermal dysplasia syndrome	skos:exactMatch	DOID:0060773	cleft lip-palate-ectodermal dysplasia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009154	hypothyroidism, congenital, nongoitrous, 5	skos:exactMatch	DOID:0070125	congenital nongoitrous hypothyroidism 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0009155	EEM syndrome	skos:exactMatch	DOID:0111649	ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009159	Ehlers-Danlos syndrome, cardiac valvular type	skos:exactMatch	DOID:0080730	Ehlers-Danlos syndrome cardiac valvular type	semapv:ManualMappingCuration	2023-06-18
MONDO:0009161	Ehlers-Danlos syndrome, dermatosparaxis type	skos:exactMatch	DOID:0080733	Ehlers-Danlos syndrome dermatosparaxis type	semapv:ManualMappingCuration	2023-06-18
MONDO:0009162	Ellis-van Creveld syndrome	skos:exactMatch	DOID:12714	Ellis-Van Creveld syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009166	pontocerebellar hypoplasia type 4	skos:exactMatch	DOID:0060273	pontocerebellar hypoplasia type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0009168	Fowler syndrome	skos:exactMatch	DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009173	congenital enteropathy due to enteropeptidase deficiency	skos:exactMatch	DOID:0111667	enterokinase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009176	epidermodysplasia verruciformis	skos:exactMatch	DOID:13777	epidermodysplasia verruciformis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009179	recessive dystrophic epidermolysis bullosa	skos:exactMatch	DOID:0060642	recessive dystrophic epidermolysis bullosa	semapv:ManualMappingCuration	2023-03-17
MONDO:0009181	epidermolysis bullosa simplex 5B, with muscular dystrophy	skos:exactMatch	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009182	junctional epidermolysis bullosa Herlitz type	skos:exactMatch	DOID:0060737	junctional epidermolysis bullosa Herlitz type	semapv:ManualMappingCuration	2023-03-17
MONDO:0009183	junctional epidermolysis bullosa with pyloric atresia	skos:exactMatch	DOID:0060733	junctional epidermolysis bullosa with pyloric atresia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009185	amelocerebrohypohidrotic syndrome	skos:exactMatch	DOID:0111668	Kohlschutter-Tonz syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009189	multiple epiphyseal dysplasia type 4	skos:exactMatch	DOID:0070300	multiple epiphyseal dysplasia 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0009192	Wolcott-Rallison syndrome	skos:exactMatch	DOID:0090060	Wolcott-Rallison syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009210	congenital factor V deficiency	skos:exactMatch	DOID:2216	factor V deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009211	congenital factor VII deficiency	skos:exactMatch	DOID:2215	factor VII deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009212	congenital factor X deficiency	skos:exactMatch	DOID:2222	factor X deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009213	Fanconi anemia complementation group C	skos:exactMatch	DOID:0111087	Fanconi anemia complementation group C	semapv:ManualMappingCuration	2023-03-17
MONDO:0009214	Fanconi anemia complementation group D2	skos:exactMatch	DOID:0111083	Fanconi anemia complementation group D2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009218	Farber lipogranulomatosis	skos:exactMatch	DOID:0050464	Farber lipogranulomatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009223	hypogonadotropic hypogonadism 23 with or without anosmia	skos:exactMatch	DOID:0090091	hypogonadotropic hypogonadism 23 with or without anosmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009226	fibrochondrogenesis 1	skos:exactMatch	DOID:0080672	fibrochondrogenesis 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0009229	hyaline fibromatosis syndrome	skos:exactMatch	DOID:0111669	hyaline fibromatosis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009231	acromesomelic dysplasia 2B	skos:exactMatch	DOID:0050790	fibular hypoplasia and complex brachydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0009232	Fuhrmann syndrome	skos:exactMatch	DOID:0090067	Fuhrmann syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009234	congenital high-molecular-weight kininogen deficiency	skos:exactMatch	DOID:0111676	high molecular weight kininogen deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009235	familial benign flecked retina	skos:exactMatch	DOID:0111677	familial benign fleck retina	semapv:ManualMappingCuration	2023-03-17
MONDO:0009238	hereditary folate malabsorption	skos:exactMatch	DOID:0111678	hereditary folate malabsorption	semapv:ManualMappingCuration	2023-03-17
MONDO:0009239	hypogonadotropic hypogonadism 24 without anosmia	skos:exactMatch	DOID:0090088	hypogonadotropic hypogonadism 24 without anosmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009240	formiminoglutamic aciduria	skos:exactMatch	DOID:0111679	glutamate formiminotransferase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009242	brittle cornea syndrome	skos:exactMatch	DOID:14775	brittle cornea syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009249	hereditary fructose intolerance	skos:exactMatch	DOID:9869	hereditary fructose intolerance syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009251	fructose-1,6-bisphosphatase deficiency	skos:exactMatch	DOID:5204	fructose-1,6-bisphosphatase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009252	essential fructosuria	skos:exactMatch	DOID:0111680	essential fructosuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009254	fucosidosis	skos:exactMatch	DOID:14500	fucosidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009255	galactokinase deficiency	skos:exactMatch	DOID:14695	galactokinase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009257	galactose epimerase deficiency	skos:exactMatch	DOID:0111458	galactose epimerase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009258	classic galactosemia	skos:exactMatch	DOID:0111459	classic galactosemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009259	gamma-glutamylcysteine synthetase deficiency	skos:exactMatch	DOID:0111681	glutamate-cysteine ligase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009260	GM1 gangliosidosis type 1	skos:exactMatch	DOID:0080502	GM1 gangliosidosis type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009261	GM1 gangliosidosis type 2	skos:exactMatch	DOID:0080501	GM1 gangliosidosis type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009262	GM1 gangliosidosis type 3	skos:exactMatch	DOID:0080489	GM1 gangliosidosis type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009263	GAPO syndrome	skos:exactMatch	DOID:0112249	GAPO syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009265	Gaucher disease type I	skos:exactMatch	DOID:0110957	Gaucher's disease type I	semapv:ManualMappingCuration	2023-03-17
MONDO:0009266	Gaucher disease type II	skos:exactMatch	DOID:0110958	Gaucher's disease type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0009267	Gaucher disease type III	skos:exactMatch	DOID:0110959	Gaucher's disease type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0009268	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome	skos:exactMatch	DOID:0112250	Gaucher's disease type IIIC	semapv:ManualMappingCuration	2023-04-17
MONDO:0009271	geroderma osteodysplastica	skos:exactMatch	DOID:0111266	geroderma osteodysplasticum	semapv:ManualMappingCuration	2023-03-17
MONDO:0009274	ghosal hematodiaphyseal dysplasia	skos:exactMatch	DOID:0112251	Ghosal hematodiaphyseal syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0009276	Bernard-Soulier syndrome	skos:exactMatch	DOID:2217	Bernard-Soulier syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009279	triple-A syndrome	skos:exactMatch	DOID:0050602	triple-A syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009281	glutaryl-CoA dehydrogenase deficiency	skos:exactMatch	DOID:0111254	glutaric acidemia I	semapv:ManualMappingCuration	2023-03-17
MONDO:0009282	multiple acyl-CoA dehydrogenase deficiency	skos:exactMatch	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009283	glutaric acidemia type 3	skos:exactMatch	DOID:0112246	glutaric acidemia type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009284	glutathione synthetase deficiency without 5-oxoprolinuria	skos:exactMatch	DOID:0112252	glutathione synthetase deficiency of erythrocytes	semapv:ManualMappingCuration	2023-04-17
MONDO:0009285	gamma-glutamyl transpeptidase deficiency	skos:exactMatch	DOID:0111257	gamma-glutamyl transpeptidase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009287	glycogen storage disease due to glucose-6-phosphatase deficiency type IA	skos:exactMatch	DOID:2749	glycogen storage disease Ia	semapv:ManualMappingCuration	2023-08-20
MONDO:0009288	glycogen storage disease Ib	skos:exactMatch	DOID:0081330	glycogen storage disease Ib	semapv:ManualMappingCuration	2023-05-21
MONDO:0009288	glycogen storage disease Ib	skos:exactMatch	DOID:0081331	glycogen storage disease Ic	semapv:ManualMappingCuration	2023-06-18
MONDO:0009290	glycogen storage disease II	skos:exactMatch	DOID:2752	glycogen storage disease II	semapv:ManualMappingCuration	2023-03-17
MONDO:0009291	glycogen storage disease III	skos:exactMatch	DOID:2748	glycogen storage disease III	semapv:ManualMappingCuration	2023-03-17
MONDO:0009292	glycogen storage disease due to glycogen branching enzyme deficiency	skos:exactMatch	DOID:2750	glycogen storage disease IV	semapv:ManualMappingCuration	2023-03-17
MONDO:0009293	glycogen storage disease V	skos:exactMatch	DOID:2746	glycogen storage disease V	semapv:ManualMappingCuration	2023-03-17
MONDO:0009294	glycogen storage disease VI	skos:exactMatch	DOID:2754	glycogen storage disease VI	semapv:ManualMappingCuration	2023-03-17
MONDO:0009295	glycogen storage disease VII	skos:exactMatch	DOID:11721	glycogen storage disease VII	semapv:ManualMappingCuration	2023-03-17
MONDO:0009297	familial renal glucosuria	skos:exactMatch	DOID:9432	renal glycosuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009299	46 XX gonadal dysgenesis	skos:exactMatch	DOID:14450	46 XX gonadal dysgenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009305	granulocytopenia with immunoglobulin abnormality	skos:exactMatch	DOID:0111974	immunodeficiency 59	semapv:ManualMappingCuration	2023-04-17
MONDO:0009306	combined immunodeficiency with skin granulomas	skos:exactMatch	DOID:0112253	combined cellular and humoral immune defects with granulomas	semapv:ManualMappingCuration	2023-04-17
MONDO:0009315	congenital factor XII deficiency	skos:exactMatch	DOID:2231	factor XII deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009318	Hallermann-Streiff syndrome	skos:exactMatch	DOID:4534	Hallermann-Streiff syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009319	pantothenate kinase-associated neurodegeneration	skos:exactMatch	DOID:3981	pantothenate kinase-associated neurodegeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0009324	Hartnup disease	skos:exactMatch	DOID:1060	Hartnup disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009326	congenital heart block	skos:exactMatch	DOID:990	congenital heart block	semapv:ManualMappingCuration	2023-03-17
MONDO:0009329	pulmonary venoocclusive disease 2	skos:exactMatch	DOID:0081269	pulmonary venoocclusive disease 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0009338	hepatic veno-occlusive disease-immunodeficiency syndrome	skos:exactMatch	DOID:0112254	hepatic venoocclusive disease with immunodeficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0009339	congenital bile acid synthesis defect 2	skos:exactMatch	DOID:0111069	congenital bile acid synthesis defect 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009341	Mowat-Wilson syndrome	skos:exactMatch	DOID:0060485	Mowat-Wilson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009345	histidinemia	skos:exactMatch	DOID:0060168	histidinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009350	Holzgreve-Wagner-Rehder syndrome	skos:exactMatch	DOID:0060566	Holzgreve-Wagner-Rehder syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009351	homocarnosinosis	skos:exactMatch	DOID:0060177	homocarnosinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009354	methylcobalamin deficiency type cblE	skos:exactMatch	DOID:0050732	methylmalonic aciduria and homocystinuria type cblE	semapv:ManualMappingCuration	2023-03-17
MONDO:0009354	methylcobalamin deficiency type cblE	skos:exactMatch	DOID:0112255	homocystinuria-megaloblastic anemia cblE type	semapv:ManualMappingCuration	2023-04-17
MONDO:0009359	multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome	skos:exactMatch	DOID:0080327	multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0009364	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1	skos:exactMatch	DOID:0111237	congenital muscular dystrophy-dystroglycanopathy type A1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009367	McKusick-Kaufman syndrome	skos:exactMatch	DOID:0111255	McKusick-Kaufman syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009370	L-2-hydroxyglutaric aciduria	skos:exactMatch	DOID:0050574	L-2-hydroxyglutaric aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009372	encephalopathy due to hydroxykynureninuria	skos:exactMatch	DOID:0112257	hydroxykynureninuria	semapv:ManualMappingCuration	2023-04-17
MONDO:0009377	hyperammonemia due to N-acetylglutamate synthase deficiency	skos:exactMatch	DOID:0112258	N-acetylglutamate synthase deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0009380	Dubin-Johnson syndrome	skos:exactMatch	DOID:12308	Dubin-Johnson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009387	familial lipoprotein lipase deficiency	skos:exactMatch	DOID:14118	familial lipoprotein lipase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009388	hyperlysinemia	skos:exactMatch	DOID:9274	hyperlysinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009393	ornithine translocase deficiency	skos:exactMatch	DOID:0050720	ornithine translocase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009394	juvenile Paget disease	skos:exactMatch	DOID:0081368	Paget's disease of bone 5	semapv:ManualMappingCuration	2023-07-09
MONDO:0009395	hyperostosis corticalis generalisata	skos:exactMatch	DOID:0080036	SOST-related sclerosing bone dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009400	hyperprolinemia type 1	skos:exactMatch	DOID:0080542	hyperprolinemia type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009401	hyperprolinemia type 2	skos:exactMatch	DOID:0080543	hyperprolinemia type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009404	hypertelorism, microtia, facial clefting syndrome	skos:exactMatch	DOID:14670	hypertelorism, microtia, facial clefting syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009406	hypertrichotic osteochondrodysplasia Cantu type	skos:exactMatch	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type	semapv:ManualMappingCuration	2023-03-17
MONDO:0009411	autoimmune polyendocrine syndrome type 1	skos:exactMatch	DOID:0050167	autoimmune polyendocrine syndrome type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009413	immunodeficiency, common variable, 2	skos:exactMatch	DOID:0081145	common variable immunodeficiency 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0009416	hypoinsulinemic hypoglycemia and body hemihypertrophy	skos:exactMatch	DOID:0112263	hypoinsulinemic hypoglycemia with hemihypertrophy	semapv:ManualMappingCuration	2023-04-17
MONDO:0009419	Woodhouse-Sakati syndrome	skos:exactMatch	DOID:0112264	Woodhouse-Sakati syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009426	hypoparathyroidism-retardation-dysmorphism syndrome	skos:exactMatch	DOID:0060348	hypoparathyroidism-retardation-dysmorphism syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009431	hereditary hypophosphatemic rickets with hypercalciuria	skos:exactMatch	DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009437	Bamforth-Lazarus syndrome	skos:exactMatch	DOID:0050655	Bamforth-Lazarus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009443	autosomal recessive congenital ichthyosis 4B	skos:exactMatch	DOID:0060713	autosomal recessive congenital ichthyosis 4B	semapv:ManualMappingCuration	2023-03-17
MONDO:0009448	iminoglycinuria	skos:exactMatch	DOID:0112265	iminoglycinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009451	Nezelof syndrome	skos:exactMatch	DOID:2012	Nezelof syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009452	Vici syndrome	skos:exactMatch	DOID:0060356	Vici syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009458	Schimke immuno-osseous dysplasia	skos:exactMatch	DOID:0060490	Schimke immuno-osseous dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009461	spermatogenic failure 5	skos:exactMatch	DOID:0070183	spermatogenic failure 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0009465	multiple intestinal atresia	skos:exactMatch	DOID:14671	multiple intestinal atresia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009469	benign recurrent intrahepatic cholestasis type 1	skos:exactMatch	DOID:0070231	benign recurrent intrahepatic cholestasis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009470	Baraitser-Winter syndrome 1	skos:exactMatch	DOID:0081112	Baraitser-Winter syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0009475	isovaleric acidemia	skos:exactMatch	DOID:14753	isovaleric acidemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009478	combined immunodeficiency due to DOCK8 deficiency	skos:exactMatch	DOID:0080594	hyper IgE recurrent infection syndrome 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0009479	Johanson-Blizzard syndrome	skos:exactMatch	DOID:14694	Johanson-Blizzard syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009482	hypogonadotropic hypogonadism 3 with or without anosmia	skos:exactMatch	DOID:0090092	hypogonadotropic hypogonadism 3 with or without anosmia	semapv:ManualMappingCuration	2023-11-19
MONDO:0009485	oculocerebrofacial syndrome, Kaufman type	skos:exactMatch	DOID:0111456	Kaufman oculocerebrofacial syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009486	autosomal recessive Kenny-Caffey syndrome	skos:exactMatch	DOID:0080722	Kenny-Caffey syndrome type 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0009490	Papillon-Lefevre disease	skos:exactMatch	DOID:3389	Papillon-Lefevre disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009499	Krabbe disease	skos:exactMatch	DOID:10587	Krabbe disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009504	mitochondrial DNA depletion syndrome 9	skos:exactMatch	DOID:0080128	mitochondrial DNA depletion syndrome 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0009511	Larsen-like syndrome, B3GAT3 type	skos:exactMatch	DOID:0080575	Larsen-like syndrome B3GAT3 type	semapv:ManualMappingCuration	2023-03-17
MONDO:0009514	Laurence-Moon syndrome	skos:exactMatch	DOID:1930	Laurence-Moon syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009515	Norum disease	skos:exactMatch	DOID:1391	Norum disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009517	Donohue syndrome	skos:exactMatch	DOID:0050470	Donohue syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009520	3-hydroxy-3-methylglutaric aciduria	skos:exactMatch	DOID:0070541	3-hydroxy-3-methylglutaryl-CoA lyase deficiency	semapv:ManualMappingCuration	2024-07-21
MONDO:0009525	split hand-foot malformation 3	skos:exactMatch	DOID:0090025	split hand-foot malformation 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009528	chylomicron retention disease	skos:exactMatch	DOID:0060357	chylomicron retention disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009530	lipoid proteinosis	skos:exactMatch	DOID:14498	lipoid proteinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009532	Miller-Dieker lissencephaly syndrome	skos:exactMatch	DOID:0060469	Miller-Dieker lissencephaly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009548	renal hypomagnesemia 5 with ocular involvement	skos:exactMatch	DOID:0060881	renal hypomagnesemia 5 with ocular involvement	semapv:ManualMappingCuration	2023-03-17
MONDO:0009550	renal hypomagnesemia 3	skos:exactMatch	DOID:0060880	renal hypomagnesemia 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009552	mal de Meleda	skos:exactMatch	DOID:0060862	mal de Meleda	semapv:ManualMappingCuration	2023-03-17
MONDO:0009557	mandibuloacral dysplasia with type A lipodystrophy	skos:exactMatch	DOID:0081128	mandibuloacral dysplasia type A lipodystrophy	semapv:ManualMappingCuration	2023-06-18
MONDO:0009561	alpha-mannosidosis	skos:exactMatch	DOID:3413	alpha-mannosidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009562	beta-mannosidosis	skos:exactMatch	DOID:3633	beta-mannosidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009563	maple syrup urine disease	skos:exactMatch	DOID:9269	maple syrup urine disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009567	Marinesco-Sjogren syndrome	skos:exactMatch	DOID:0080195	Marinesco-Sjogren syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009568	mast syndrome	skos:exactMatch	DOID:0060245	MAST syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009575	thiamine-responsive megaloblastic anemia syndrome	skos:exactMatch	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009576	megalocornea	skos:exactMatch	DOID:0060305	megalocornea	semapv:ManualMappingCuration	2023-03-17
MONDO:0009579	Frank-Ter Haar syndrome	skos:exactMatch	DOID:0111789	Frank-Ter Haar syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009580	intellectual disability, autosomal recessive 1	skos:exactMatch	DOID:0081177	autosomal recessive intellectual developmental disorder 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0009593	spondylometaphyseal dysplasia, Sedaghatian type	skos:exactMatch	DOID:0112298	spondylometaphyseal dysplasia Sedaghatian type	semapv:ManualMappingCuration	2023-06-18
MONDO:0009595	cartilage-hair hypoplasia	skos:exactMatch	DOID:14773	cartilage-hair hypoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009603	3-hydroxyisobutyryl-CoA hydrolase deficiency	skos:exactMatch	DOID:0060949	3-hydroxyisobutryl-CoA hydrolase deficiency	semapv:ManualMappingCuration	2024-07-21
MONDO:0009609	methylcobalamin deficiency type cblG	skos:exactMatch	DOID:0050733	methylmalonic aciduria and homocystinuria type cblG	semapv:ManualMappingCuration	2023-03-17
MONDO:0009609	methylcobalamin deficiency type cblG	skos:exactMatch	DOID:0112256	homocystinuria-megaloblastic anemia cblG type	semapv:ManualMappingCuration	2023-04-17
MONDO:0009610	3-methylglutaconic aciduria type 1	skos:exactMatch	DOID:0110002	3-methylglutaconic aciduria type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009611	3-methylglutaconic aciduria type 4	skos:exactMatch	DOID:0110006	3-methylglutaconic aciduria type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0009612	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency	skos:exactMatch	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009613	methylmalonic aciduria, cblA type	skos:exactMatch	DOID:0060742	methylmalonic acidemia cblA type	semapv:ManualMappingCuration	2023-03-17
MONDO:0009614	methylmalonic aciduria, cblB type	skos:exactMatch	DOID:0060743	methylmalonic acidemia cblB type	semapv:ManualMappingCuration	2023-03-17
MONDO:0009617	microcephaly 1, primary, autosomal recessive	skos:exactMatch	DOID:0070285	primary autosomal recessive microcephaly 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009619	microcephaly-micromelia syndrome	skos:exactMatch	DOID:0081432	microcephaly-micromelia syndrome	semapv:ManualMappingCuration	2024-05-19
MONDO:0009623	Nijmegen breakage syndrome	skos:exactMatch	DOID:7400	Nijmegen breakage syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009624	microcephaly and chorioretinopathy 1	skos:exactMatch	DOID:0080105	microcephaly and chorioretinopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009626	pseudo-TORCH syndrome	skos:exactMatch	DOID:0050656	pseudo-TORCH syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009627	Galloway-Mowat syndrome	skos:exactMatch	DOID:0080694	Galloway-Mowat syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009635	microvillus inclusion disease	skos:exactMatch	DOID:0060775	microvillus inclusion disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009636	mitochondrial DNA depletion syndrome 3 (hepatocerebral type)	skos:exactMatch	DOID:0080121	mitochondrial DNA depletion syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009637	inborn mitochondrial myopathy	skos:exactMatch	DOID:699	mitochondrial myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009642	orofaciodigital syndrome type II	skos:exactMatch	DOID:0060959	orofaciodigital syndrome II	semapv:ManualMappingCuration	2024-07-21
MONDO:0009643	sulfite oxidase deficiency due to molybdenum cofactor deficiency type A	skos:exactMatch	DOID:0111164	molybdenum cofactor deficiency type A	semapv:ManualMappingCuration	2023-03-17
MONDO:0009644	sulfite oxidase deficiency due to molybdenum cofactor deficiency type B	skos:exactMatch	DOID:0111163	molybdenum cofactor deficiency type B	semapv:ManualMappingCuration	2023-03-17
MONDO:0009650	mucolipidosis type II	skos:exactMatch	DOID:0080070	mucolipidosis II alpha/beta	semapv:ManualMappingCuration	2023-03-17
MONDO:0009652	GNPTG-mucolipidosis	skos:exactMatch	DOID:0080678	mucolipidosis III gamma	semapv:ManualMappingCuration	2023-06-18
MONDO:0009653	mucolipidosis type IV	skos:exactMatch	DOID:0080490	mucolipidosis type IV	semapv:ManualMappingCuration	2023-03-17
MONDO:0009655	mucopolysaccharidosis type 3A	skos:exactMatch	DOID:0111395	mucopolysaccharidosis type IIIA	semapv:ManualMappingCuration	2023-03-17
MONDO:0009656	mucopolysaccharidosis type 3B	skos:exactMatch	DOID:0111394	mucopolysaccharidosis type IIIB	semapv:ManualMappingCuration	2023-03-17
MONDO:0009657	mucopolysaccharidosis type 3C	skos:exactMatch	DOID:0111393	mucopolysaccharidosis type IIIC	semapv:ManualMappingCuration	2023-03-17
MONDO:0009658	mucopolysaccharidosis type 3D	skos:exactMatch	DOID:0111402	mucopolysaccharidosis type IIID	semapv:ManualMappingCuration	2023-03-17
MONDO:0009659	mucopolysaccharidosis type 4A	skos:exactMatch	DOID:0111391	mucopolysaccharidosis IVA	semapv:ManualMappingCuration	2023-03-17
MONDO:0009660	mucopolysaccharidosis type 4B	skos:exactMatch	DOID:0111392	mucopolysaccharidosis type IVB	semapv:ManualMappingCuration	2023-03-17
MONDO:0009661	mucopolysaccharidosis type 6	skos:exactMatch	DOID:12800	mucopolysaccharidosis VI	semapv:ManualMappingCuration	2023-03-17
MONDO:0009662	mucopolysaccharidosis type 7	skos:exactMatch	DOID:12803	Sly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009664	mulibrey nanism	skos:exactMatch	DOID:0050436	mulibrey nanism	semapv:ManualMappingCuration	2023-03-17
MONDO:0009665	biotinidase deficiency	skos:exactMatch	DOID:856	biotinidase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009666	holocarboxylase synthetase deficiency	skos:exactMatch	DOID:859	holocarboxylase synthetase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009667	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3	skos:exactMatch	DOID:0111236	congenital muscular dystrophy-dystroglycanopathy type A3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009669	spinal muscular atrophy, type 1	skos:exactMatch	DOID:13137	Werdnig-Hoffmann disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009670	lethal congenital contracture syndrome 1	skos:exactMatch	DOID:0060559	lethal congenital contracture syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009672	spinal muscular atrophy, type III	skos:exactMatch	DOID:12376	juvenile spinal muscular atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009673	spinal muscular atrophy, type II	skos:exactMatch	DOID:0050530	intermediate spinal muscular atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009675	autosomal recessive limb-girdle muscular dystrophy type 2A	skos:exactMatch	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0009676	autosomal recessive limb-girdle muscular dystrophy type 2B	skos:exactMatch	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B	semapv:ManualMappingCuration	2023-03-17
MONDO:0009677	autosomal recessive limb-girdle muscular dystrophy type 2C	skos:exactMatch	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C	semapv:ManualMappingCuration	2023-03-17
MONDO:0009678	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4	skos:exactMatch	DOID:0050559	Fukuyama congenital muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009679	arthrogryposis due to muscular dystrophy	skos:exactMatch	DOID:0110631	arthrogryposis due to muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009681	Ullrich congenital muscular dystrophy 1A	skos:exactMatch	DOID:0060946	Ullrich congenital muscular dystrophy 1A	semapv:ManualMappingCuration	2024-08-18
MONDO:0009683	autosomal recessive limb-girdle muscular dystrophy type 2H	skos:exactMatch	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H	semapv:ManualMappingCuration	2023-03-17
MONDO:0009685	Miyoshi myopathy	skos:exactMatch	DOID:0070198	Miyoshi muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009696	juvenile myoclonic epilepsy	skos:exactMatch	DOID:4890	juvenile myoclonic epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009697	Lafora disease	skos:exactMatch	DOID:3534	Lafora disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009698	Unverricht-Lundborg syndrome	skos:exactMatch	DOID:0111452	progressive myoclonus epilepsy 1A	semapv:ManualMappingCuration	2023-06-18
MONDO:0009698	Unverricht-Lundborg syndrome	skos:exactMatch	DOID:3535	Unverricht-Lundborg syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009699	action myoclonus-renal failure syndrome	skos:exactMatch	DOID:0111444	progressive myoclonus epilepsy 4	semapv:ManualMappingCuration	2023-04-17
MONDO:0009705	carnitine palmitoyl transferase 1A deficiency	skos:exactMatch	DOID:0090129	carnitine palmitoyltransferase I deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009709	myopathy, centronuclear, 2	skos:exactMatch	DOID:0111220	centronuclear myopathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009710	Thomsen and Becker disease	skos:exactMatch	DOID:2106	myotonia congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0009711	congenital fiber-type disproportion myopathy	skos:exactMatch	DOID:0080102	congenital myopathy 4A	semapv:ManualMappingCuration	2023-03-17
MONDO:0009720	Keipert syndrome	skos:exactMatch	DOID:0111842	Keipert syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009722	Bailey-Bloch congenital myopathy	skos:exactMatch	DOID:0060346	Native American myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009723	Leigh syndrome	skos:exactMatch	DOID:3652	Leigh disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009726	proteosome-associated autoinflammatory syndrome	skos:exactMatch	DOID:0050553	proteasome-associated autoinflammatory syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009726	proteosome-associated autoinflammatory syndrome	skos:exactMatch	DOID:0060913	proteosome-associated autoinflammatory syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0009728	nephronophthisis 1	skos:exactMatch	DOID:0111112	nephronophthisis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009732	congenital nephrotic syndrome, Finnish type	skos:exactMatch	DOID:0080390	nephrotic syndrome type 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0009733	nephrotic syndrome, type 4	skos:exactMatch	DOID:0080383	nephrotic syndrome type 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0009734	hyperinsulinemic hypoglycemia, familial, 1	skos:exactMatch	DOID:0070219	familial hyperinsulinemic hypoglycemia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009735	Netherton syndrome	skos:exactMatch	DOID:0050474	Netherton syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009736	Neu-Laxova syndrome 1	skos:exactMatch	DOID:0080076	Neu-Laxova syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0009737	galactosialidosis	skos:exactMatch	DOID:0080540	galactosialidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009738	sialidosis type 2	skos:exactMatch	DOID:3343	glycoproteinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009744	neuronal ceroid lipofuscinosis 1	skos:exactMatch	DOID:0110721	neuronal ceroid lipofuscinosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009745	neuronal ceroid lipofuscinosis 5	skos:exactMatch	DOID:0110728	neuronal ceroid lipofuscinosis 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0009746	hereditary sensory and autonomic neuropathy type 4	skos:exactMatch	DOID:0070146	hereditary sensory neuropathy type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0009747	mitochondrial DNA depletion syndrome 6 (hepatocerebral type)	skos:exactMatch	DOID:0080125	mitochondrial DNA depletion syndrome 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0009756	Niemann-Pick disease type A	skos:exactMatch	DOID:0070111	Niemann-Pick disease type A	semapv:ManualMappingCuration	2023-03-17
MONDO:0009760	Norman-Roberts syndrome	skos:exactMatch	DOID:0060902	Norman-Roberts syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009762	nystagmus, congenital, autosomal recessive	skos:exactMatch	DOID:0111797	autosomal recessive congenital nystagmus	semapv:ManualMappingCuration	2023-11-19
MONDO:0009764	ocular motor apraxia, Cogan type	skos:exactMatch	DOID:0080849	ocular motor apraxia, Cogan type	semapv:ManualMappingCuration	2023-03-17
MONDO:0009774	cloacal exstrophy	skos:exactMatch	DOID:0080175	cloacal exstrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009776	spermatogenic failure 1	skos:exactMatch	DOID:0070188	spermatogenic failure 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009779	autosomal recessive omodysplasia	skos:exactMatch	DOID:0080844	omodysplasia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0009783	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1	skos:exactMatch	DOID:0111522	autosomal recessive progressive external ophthalmoplegia 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0009786	optic atrophy 6	skos:exactMatch	DOID:0111435	optic atrophy 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0009787	3-methylglutaconic aciduria type 3	skos:exactMatch	DOID:0110004	3-methylglutaconic aciduria type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009793	orofaciodigital syndrome III	skos:exactMatch	DOID:0060373	orofaciodigital syndrome III	semapv:ManualMappingCuration	2023-03-17
MONDO:0009794	orofaciodigital syndrome IV	skos:exactMatch	DOID:0060374	orofaciodigital syndrome IV	semapv:ManualMappingCuration	2023-03-17
MONDO:0009795	orofaciodigital syndrome IX	skos:exactMatch	DOID:0060382	orofaciodigital syndrome IX	semapv:ManualMappingCuration	2023-03-17
MONDO:0009796	ornithine aminotransferase deficiency	skos:exactMatch	DOID:1415	gyrate atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009797	orotic aciduria	skos:exactMatch	DOID:0050833	orotic aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009804	osteogenesis imperfecta type 3	skos:exactMatch	DOID:0110339	osteogenesis imperfecta type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009813	chronic recurrent multifocal osteomyelitis	skos:exactMatch	DOID:0060645	chronic recurrent multifocal osteomyelitis	semapv:ManualMappingCuration	2024-02-18
MONDO:0009815	autosomal recessive osteopetrosis 1	skos:exactMatch	DOID:0110942	autosomal recessive osteopetrosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009816	autosomal recessive osteopetrosis 2	skos:exactMatch	DOID:0110943	autosomal recessive osteopetrosis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009818	autosomal recessive osteopetrosis 3	skos:exactMatch	DOID:0110941	autosomal recessive osteopetrosis 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009820	osteoporosis-pseudoglioma syndrome	skos:exactMatch	DOID:0060849	osteoporosis-pseudoglioma syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009823	primary hyperoxaluria type 1	skos:exactMatch	DOID:0111670	primary hyperoxaluria type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009824	primary hyperoxaluria type 2	skos:exactMatch	DOID:0111671	primary hyperoxaluria type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009830	parkinsonian-pyramidal syndrome	skos:exactMatch	DOID:0060372	Parkinson's disease 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0009832	pancreatic agenesis	skos:exactMatch	DOID:0050877	pancreatic agenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009833	Shwachman-Diamond syndrome	skos:exactMatch	DOID:0060479	Shwachman-Diamond syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009837	choroid plexus papilloma	skos:exactMatch	DOID:2626	choroid plexus papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0009841	PEHO syndrome	skos:exactMatch	DOID:0080539	PEHO syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009843	hypomyelinating leukodystrophy 3	skos:exactMatch	DOID:0060790	hypomyelinating leukodystrophy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0009846	pentosuria	skos:exactMatch	DOID:0111258	pentosuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009849	hyperimmunoglobulinemia D with periodic fever	skos:exactMatch	DOID:0081450	hyperimmunoglobulinemia D periodic fever syndrome	semapv:ManualMappingCuration	2024-05-19
MONDO:0009852	hereditary intrinsic factor deficiency	skos:exactMatch	DOID:0050734	congenital intrinsic factor deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009855	d-bifunctional protein deficiency	skos:exactMatch	DOID:0090031	D-bifunctional protein deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009856	Peters plus syndrome	skos:exactMatch	DOID:0080201	Peters plus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009857	persistent Mullerian duct syndrome	skos:exactMatch	DOID:0050791	persistent Mullerian duct syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009861	phenylketonuria	skos:exactMatch	DOID:9281	phenylketonuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009862	dihydropteridine reductase deficiency	skos:exactMatch	DOID:0081130	BH4-deficient hyperphenylalaninemia C	semapv:ManualMappingCuration	2023-06-18
MONDO:0009863	BH4-deficient hyperphenylalaninemia A	skos:exactMatch	DOID:0090106	BH4-deficient hyperphenylalaninemia A	semapv:ManualMappingCuration	2023-03-17
MONDO:0009867	lethal congenital glycogen storage disease of heart	skos:exactMatch	DOID:0090101	lethal congenital glycogen storage disease of heart	semapv:ManualMappingCuration	2023-03-17
MONDO:0009868	glycogen storage disease IXb	skos:exactMatch	DOID:0111041	glycogen storage disease IXB	semapv:ManualMappingCuration	2023-03-17
MONDO:0009872	Bjornstad syndrome	skos:exactMatch	DOID:0050677	Bjornstad syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009876	isolated growth hormone deficiency type IA	skos:exactMatch	DOID:0060873	isolated growth hormone deficiency type IA	semapv:ManualMappingCuration	2023-03-17
MONDO:0009877	Laron syndrome	skos:exactMatch	DOID:9521	Laron syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009883	alpha-2-plasmin inhibitor deficiency	skos:exactMatch	DOID:0060601	alpha-2-plasmin inhibitor deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009885	Scott syndrome	skos:exactMatch	DOID:0111052	Scott syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009889	autosomal recessive polycystic kidney disease	skos:exactMatch	DOID:0110861	autosomal recessive polycystic kidney disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009892	Chuvash polycythemia	skos:exactMatch	DOID:0060474	familial erythrocytosis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0009894	short-rib thoracic dysplasia 6 with or without polydactyly	skos:exactMatch	DOID:0110092	short-rib thoracic dysplasia 6 with or without polydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0009902	cutaneous porphyria	skos:exactMatch	DOID:13271	cutaneous porphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0009903	postaxial acrofacial dysostosis	skos:exactMatch	DOID:0111259	postaxial acrofacial dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009904	Gitelman syndrome	skos:exactMatch	DOID:0050450	Gitelman syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009908	pterin-4 alpha-carbinolamine dehydratase 1 deficiency	skos:exactMatch	DOID:0081131	BH4-deficient hyperphenylalaninemia D	semapv:ManualMappingCuration	2023-06-18
MONDO:0009910	Wiedemann-Rautenstrauch syndrome	skos:exactMatch	DOID:0081333	Wiedemann-Rautenstrauch syndrome	semapv:ManualMappingCuration	2023-05-21
MONDO:0009916	46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency	skos:exactMatch	DOID:0112248	17-beta hydroxysteroid dehydrogenase 3 deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0009917	autosomal recessive pseudohypoaldosteronism type 1	skos:exactMatch	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009919	peroxisomal acyl-CoA oxidase deficiency	skos:exactMatch	DOID:0050797	peroxisomal acyl-CoA oxidase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0009925	autosomal recessive inherited pseudoxanthoma elasticum	skos:exactMatch	DOID:2738	pseudoxanthoma elasticum	semapv:ManualMappingCuration	2023-03-17
MONDO:0009928	pulmonary alveolar microlithiasis	skos:exactMatch	DOID:12117	pulmonary alveolar microlithiasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009934	alveolar capillary dysplasia with misalignment of pulmonary veins	skos:exactMatch	DOID:13042	persistent fetal circulation syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009937	pulmonary venoocclusive disease	skos:exactMatch	DOID:5453	pulmonary venoocclusive disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009940	pycnodysostosis	skos:exactMatch	DOID:0080038	pycnodysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009943	Pyle disease	skos:exactMatch	DOID:0080019	metaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0009945	pyridoxine-dependent epilepsy	skos:exactMatch	DOID:0080768	pyridoxine-dependent epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0009947	glutathione synthetase deficiency with 5-oxoprolinuria	skos:exactMatch	DOID:0081034	glutatione synthetase deficiency with 5-oxoprolinuria	semapv:ManualMappingCuration	2023-06-18
MONDO:0009950	pyruvate kinase deficiency of red cells	skos:exactMatch	DOID:0111077	pyruvate kinase deficiency of red cells	semapv:ManualMappingCuration	2023-03-17
MONDO:0009953	leukocyte adhesion deficiency type II	skos:exactMatch	DOID:0070255	congenital disorder of glycosylation type IIc	semapv:ManualMappingCuration	2023-03-17
MONDO:0009953	leukocyte adhesion deficiency type II	skos:exactMatch	DOID:0080492	leukocyte adhesion deficiency 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0009955	rapadilino syndrome	skos:exactMatch	DOID:0050774	rapadilino syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009958	adult Refsum disease	skos:exactMatch	DOID:10582	Refsum disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0009959	peroxisome biogenesis disorder type 3B	skos:exactMatch	DOID:0081241	peroxisome biogenesis disorder 3B	semapv:ManualMappingCuration	2023-05-21
MONDO:0009960	inflammatory bowel disease 1	skos:exactMatch	DOID:0110892	inflammatory bowel disease 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0009964	short-rib thoracic dysplasia 9 with or without polydactyly	skos:exactMatch	DOID:0110097	short-rib thoracic dysplasia 9 with or without polydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0009965	Perlman syndrome	skos:exactMatch	DOID:0060476	Perlman syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009966	NPHP3-related Meckel-like syndrome	skos:exactMatch	DOID:0070121	Meckel syndrome 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0009973	reticular dysgenesis	skos:exactMatch	DOID:0060020	reticular dysgenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0009974	familial hemophagocytic lymphohistiocytosis type 1	skos:exactMatch	DOID:0110921	familial hemophagocytic lymphohistiocytosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0009990	Revesz syndrome	skos:exactMatch	DOID:0070026	Revesz syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0009999	autosomal recessive Robinow syndrome	skos:exactMatch	DOID:0060764	autosomal recessive Robinow syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010002	Rothmund-Thomson syndrome	skos:exactMatch	DOID:2732	Rothmund-Thomson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010004	EEC syndrome	skos:exactMatch	DOID:0060782	EEC syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010006	Sandhoff disease	skos:exactMatch	DOID:3323	Sandhoff disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010008	sarcosinemia	skos:exactMatch	DOID:0112307	sarcosinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010010	Schinzel-Giedion syndrome	skos:exactMatch	DOID:0070509	Schinzel Giedion syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0010013	schneckenbecken dysplasia	skos:exactMatch	DOID:0050775	schneckenbecken dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010015	anterior segment dysgenesis 7	skos:exactMatch	DOID:0080612	anterior segment dysgenesis 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0010016	sclerosteosis 1	skos:exactMatch	DOID:0060756	sclerosteosis 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0010017	sea-blue histiocyte syndrome	skos:exactMatch	DOID:4423	sea-blue histiocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0010020	congenital generalized lipodystrophy type 2	skos:exactMatch	DOID:0111136	congenital generalized lipodystrophy type 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0010023	combined immunodeficiency due to ZAP70 deficiency	skos:exactMatch	DOID:0111943	immunodeficiency 48	semapv:ManualMappingCuration	2023-04-17
MONDO:0010024	Beemer-Langer syndrome	skos:exactMatch	DOID:9249	Beemer-Langer syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010026	SHORT syndrome	skos:exactMatch	DOID:0111454	SHORT syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010028	sialuria	skos:exactMatch	DOID:3659	sialuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0010029	situs inversus	skos:exactMatch	DOID:758	situs inversus	semapv:ManualMappingCuration	2023-03-17
MONDO:0010031	Sjogren-Larsson syndrome	skos:exactMatch	DOID:14501	Sjogren-Larsson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010035	Smith-Lemli-Opitz syndrome	skos:exactMatch	DOID:14692	Smith-Lemli-Opitz syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010041	Charlevoix-Saguenay spastic ataxia	skos:exactMatch	DOID:0050946	Charlevoix-Saguenay spastic ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010043	hereditary spastic paraplegia 17	skos:exactMatch	DOID:0110770	hereditary spastic paraplegia 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0010044	hereditary spastic paraplegia 15	skos:exactMatch	DOID:0110768	hereditary spastic paraplegia 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0010046	hereditary spastic paraplegia 23	skos:exactMatch	DOID:0110774	hereditary spastic paraplegia 23	semapv:ManualMappingCuration	2023-03-17
MONDO:0010047	hereditary spastic paraplegia 5A	skos:exactMatch	DOID:0110810	hereditary spastic paraplegia 5A	semapv:ManualMappingCuration	2023-03-17
MONDO:0010053	hereditary spherocytosis type 3	skos:exactMatch	DOID:0110918	hereditary spherocytosis type 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0010056	spinal muscular atrophy, type IV	skos:exactMatch	DOID:0050529	adult spinal muscular atrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010060	mitochondrial DNA depletion syndrome 7 (hepatocerebral type)	skos:exactMatch	DOID:0080126	mitochondrial DNA depletion syndrome 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0010061	autosomal recessive cerebellar ataxia-blindness-deafness syndrome	skos:exactMatch	DOID:0111612	autosomal recessive spinocerebellar ataxia 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0010068	spondyloepimetaphyseal dysplasia, sponastrime type	skos:exactMatch	DOID:5684	spondyloepimetaphyseal dysplasia, Sponastrime type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010072	spondyloepiphyseal dysplasia tarda, autosomal recessive	skos:exactMatch	DOID:0112293	autosomal recessive spondyloepiphyseal dysplasia tarda	semapv:ManualMappingCuration	2024-04-21
MONDO:0010073	spondyloepiphyseal dysplasia tarda, Kohn type	skos:exactMatch	DOID:0112292	spondyloepiphyseal dysplasia tarda with intellectual disability	semapv:ManualMappingCuration	2023-06-18
MONDO:0010075	spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures	skos:exactMatch	DOID:0112198	spondyloepimetaphyseal dysplasia with joint laxity type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010077	spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome	skos:exactMatch	DOID:0112196	spondylometaepiphyseal dysplasia, short limb-hand type	semapv:ManualMappingCuration	2023-04-17
MONDO:0010078	spondyloperipheral dysplasia	skos:exactMatch	DOID:0112195	spondyloperipheral dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010079	Canavan disease	skos:exactMatch	DOID:3613	Canavan disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010083	succinic semialdehyde dehydrogenase deficiency	skos:exactMatch	DOID:0060175	succinic semialdehyde dehydrogenase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010088	mucosulfatidosis	skos:exactMatch	DOID:0050441	mucosulfatidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0010089	isolated sulfite oxidase deficiency	skos:exactMatch	DOID:0111270	isolated sulfite oxidase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010091	Cold-induced sweating syndrome 1	skos:exactMatch	DOID:0080329	cold-induced sweating syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010092	Filippi syndrome	skos:exactMatch	DOID:0112194	Filippi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010094	spondylocarpotarsal synostosis syndrome	skos:exactMatch	DOID:0090116	spondylocarpotarsal synostosis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010099	Tay-Sachs disease AB variant	skos:exactMatch	DOID:4795	GM2 Gangliosidosis, AB variant	semapv:ManualMappingCuration	2023-03-17
MONDO:0010100	Tay-Sachs disease	skos:exactMatch	DOID:3320	Tay-Sachs disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010110	tetraamelia-multiple malformations syndrome	skos:exactMatch	DOID:0112191	tetraamelia syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0010121	thrombocytopenia-absent radius syndrome	skos:exactMatch	DOID:14699	thrombocytopenia-absent radius syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010130	dihydropyrimidine dehydrogenase deficiency	skos:exactMatch	DOID:14218	dihydropyrimidine dehydrogenase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010132	familial thyroid dyshormonogenesis	skos:exactMatch	DOID:0112183	familial thyroid dyshormonogenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0010134	Pendred syndrome	skos:exactMatch	DOID:0060744	Pendred syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010139	isolated thyroid-stimulating hormone deficiency	skos:exactMatch	DOID:0070123	congenital nongoitrous hypothyroidism 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0010142	hypothyroidism due to TSH receptor mutations	skos:exactMatch	DOID:0070126	congenital nongoitrous hypothyroidism 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010149	transcobalamin II deficiency	skos:exactMatch	DOID:0050818	transcobalamin II deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010152	trichomegaly-retina pigmentary degeneration-dwarfism syndrome	skos:exactMatch	DOID:0111271	Oliver-McFarlane syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010156	Troyer syndrome	skos:exactMatch	DOID:0050886	Troyer syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010160	tyrosinemia type II	skos:exactMatch	DOID:0050725	tyrosinemia type II	semapv:ManualMappingCuration	2023-03-17
MONDO:0010161	tyrosinemia type I	skos:exactMatch	DOID:0050726	tyrosinemia type I	semapv:ManualMappingCuration	2023-03-17
MONDO:0010162	tyrosinemia type III	skos:exactMatch	DOID:0050727	tyrosinemia type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0010164	phocomelia, Schinzel type	skos:exactMatch	DOID:0112181	Schinzel type phocomelia	semapv:ManualMappingCuration	2023-04-17
MONDO:0010167	urocanic aciduria	skos:exactMatch	DOID:0112180	urocanase deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0010168	Usher syndrome type 1	skos:exactMatch	DOID:0110826	Usher syndrome type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010169	Usher syndrome type 2A	skos:exactMatch	DOID:0110838	Usher syndrome type 2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0010170	Usher syndrome type 3A	skos:exactMatch	DOID:0110841	Usher syndrome type 3A	semapv:ManualMappingCuration	2023-11-19
MONDO:0010171	Usher syndrome type 1C	skos:exactMatch	DOID:0110830	Usher syndrome type 1C	semapv:ManualMappingCuration	2023-03-17
MONDO:0010173	Mayer-Rokitansky-Kuster-Hauser syndrome type 1	skos:exactMatch	DOID:0112178	Mayer-Rokitansky-Kuster-Hauser syndrome type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010176	orofaciodigital syndrome type 6	skos:exactMatch	DOID:0060376	Joubert syndrome with orofaciodigital defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0010178	congenital bilateral aplasia of vas deferens from CFTR mutation	skos:exactMatch	DOID:0111864	autosomal recessive congenital bilateral absence of vas deferens	semapv:ManualMappingCuration	2023-06-18
MONDO:0010183	methylmalonic aciduria and homocystinuria type cblF	skos:exactMatch	DOID:0050717	methylmalonic aciduria and homocystinuria type cblF	semapv:ManualMappingCuration	2023-03-17
MONDO:0010184	methylmalonic aciduria and homocystinuria type cblC	skos:exactMatch	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC	semapv:ManualMappingCuration	2023-03-17
MONDO:0010185	methylmalonic aciduria and homocystinuria type cblD	skos:exactMatch	DOID:0050716	methylmalonic aciduria and homocystinuria type cblD	semapv:ManualMappingCuration	2023-03-17
MONDO:0010187	vitamin K-dependent clotting factors, combined deficiency of, type 1	skos:exactMatch	DOID:0112173	combined deficiency of vitamin K-dependent clotting factors 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0010188	familial isolated deficiency of vitamin E	skos:exactMatch	DOID:0090028	familial isolated deficiency of vitamin E	semapv:ManualMappingCuration	2023-03-17
MONDO:0010190	pontocerebellar hypoplasia type 2A	skos:exactMatch	DOID:0060267	pontocerebellar hypoplasia type 2A	semapv:ManualMappingCuration	2024-04-21
MONDO:0010191	von Willebrand disease 3	skos:exactMatch	DOID:0111054	von Willebrand's disease 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0010192	Waardenburg syndrome type 4A	skos:exactMatch	DOID:0110953	Waardenburg syndrome type 4A	semapv:ManualMappingCuration	2024-04-21
MONDO:0010193	Weaver syndrome	skos:exactMatch	DOID:14731	Weaver syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010196	Werner syndrome	skos:exactMatch	DOID:5688	Werner syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010200	Wilson disease	skos:exactMatch	DOID:893	Wilson disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010208	wrinkly skin syndrome	skos:exactMatch	DOID:0112171	wrinkly skin syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010209	xanthinuria type I	skos:exactMatch	DOID:0070452	xanthinuria type I	semapv:ManualMappingCuration	2024-04-21
MONDO:0010210	xeroderma pigmentosum group A	skos:exactMatch	DOID:0110843	xeroderma pigmentosum group A	semapv:ManualMappingCuration	2023-03-17
MONDO:0010211	xeroderma pigmentosum group C	skos:exactMatch	DOID:0110844	xeroderma pigmentosum group C	semapv:ManualMappingCuration	2023-03-17
MONDO:0010212	xeroderma pigmentosum group D	skos:exactMatch	DOID:0110845	xeroderma pigmentosum group D	semapv:ManualMappingCuration	2023-03-17
MONDO:0010213	xeroderma pigmentosum group E	skos:exactMatch	DOID:0110846	xeroderma pigmentosum group E	semapv:ManualMappingCuration	2023-03-17
MONDO:0010214	xeroderma pigmentosum variant type	skos:exactMatch	DOID:0110847	xeroderma pigmentosum variant type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010215	xeroderma pigmentosum group F	skos:exactMatch	DOID:0110848	xeroderma pigmentosum group F	semapv:ManualMappingCuration	2023-03-17
MONDO:0010216	xeroderma pigmentosum group G	skos:exactMatch	DOID:0110849	xeroderma pigmentosum group G	semapv:ManualMappingCuration	2023-03-17
MONDO:0010217	de Sanctis-Cacchione syndrome	skos:exactMatch	DOID:0112158	De Sanctis-Cacchione syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010221	CHIME syndrome	skos:exactMatch	DOID:0112152	CHIME syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010224	corpus callosum agenesis-abnormal genitalia syndrome	skos:exactMatch	DOID:0112151	corpus callosum agenesis-abnormal genitalia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010225	Dent disease type 1	skos:exactMatch	DOID:0081453	Dent disease 1	semapv:ManualMappingCuration	2024-07-21
MONDO:0010235	X-linked intellectual disability-psychosis-macroorchidism syndrome	skos:exactMatch	DOID:0060827	X-linked intellectual disability-psychosis-macroorchidism syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010239	lissencephaly type 1 due to doublecortin gene mutation	skos:exactMatch	DOID:0112239	X-linked lissencephaly 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0010241	congenital stationary night blindness 2A	skos:exactMatch	DOID:0110871	congenital stationary night blindness 2A	semapv:ManualMappingCuration	2024-04-21
MONDO:0010246	developmental and epileptic encephalopathy, 9	skos:exactMatch	DOID:0060848	developmental and epileptic encephalopathy 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0010248	X-linked spondyloepimetaphyseal dysplasia	skos:exactMatch	DOID:0112150	X-linked spondyloepimetaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010256	intellectual disability, X-linked 21	skos:exactMatch	DOID:0112022	non-syndromic X-linked intellectual disability 21	semapv:ManualMappingCuration	2023-06-18
MONDO:0010258	MEHMO syndrome	skos:exactMatch	DOID:0060801	MEHMO syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010261	microphthalmia, syndromic 2	skos:exactMatch	DOID:0111809	syndromic microphthalmia 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0010263	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome	skos:exactMatch	DOID:0111860	AMME complex	semapv:ManualMappingCuration	2023-04-17
MONDO:0010264	X-linked adrenal hypoplasia congenita	skos:exactMatch	DOID:0080156	X-linked adrenal hypoplasia congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0010265	Simpson-Golabi-Behmel syndrome type 2	skos:exactMatch	DOID:0080342	Simpson-Golabi-Behmel syndrome type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0010266	intellectual disability, X-linked 58	skos:exactMatch	DOID:0112024	non-syndromic X-linked intellectual disability 58	semapv:ManualMappingCuration	2023-06-18
MONDO:0010268	X-linked lissencephaly with abnormal genitalia	skos:exactMatch	DOID:0112238	X-linked lissencephaly 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0010269	Coats disease	skos:exactMatch	DOID:7765	Coats disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010270	syndromic X-linked intellectual disability 7	skos:exactMatch	DOID:0060808	syndromic X-linked intellectual disability 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0010277	syndromic X-linked intellectual disability Shashi type	skos:exactMatch	DOID:0060826	syndromic X-linked intellectual disability Shashi type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010278	Christianson syndrome	skos:exactMatch	DOID:0060825	Christianson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010279	terminal osseous dysplasia-pigmentary defects syndrome	skos:exactMatch	DOID:0112149	terminal osseous dysplasia	semapv:ManualMappingCuration	2023-04-17
MONDO:0010283	syndromic X-linked intellectual disability Lubs type	skos:exactMatch	DOID:0060799	syndromic X-linked intellectual disability Lubs type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010284	Armfield syndrome	skos:exactMatch	DOID:0050764	Armfield syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010285	syndromic X-linked intellectual disability Abidi type	skos:exactMatch	DOID:0060818	syndromic X-linked intellectual disability Abidi type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010286	syndromic X-linked intellectual disability Siderius type	skos:exactMatch	DOID:0060812	syndromic X-linked intellectual disability Siderius type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010287	hereditary spastic paraplegia 16	skos:exactMatch	DOID:0110769	hereditary spastic paraplegia 16	semapv:ManualMappingCuration	2023-03-17
MONDO:0010292	Uruguay Faciocardiomusculoskeletal syndrome	skos:exactMatch	DOID:0112148	Uruguay faciocardiomusculoskeletal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010293	ectodermal dysplasia and immune deficiency	skos:exactMatch	DOID:0081077	ectodermal dysplasia and immune deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010294	X-linked severe congenital neutropenia	skos:exactMatch	DOID:0112128	X-linked severe congenital neutropenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010298	Lesch-Nyhan syndrome	skos:exactMatch	DOID:1919	Lesch-Nyhan syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010299	hypoxanthine guanine phosphoribosyltransferase partial deficiency	skos:exactMatch	DOID:0112127	HRPT-related hyperuricemia	semapv:ManualMappingCuration	2023-04-17
MONDO:0010302	Ito hypomelanosis	skos:exactMatch	DOID:3156	hypomelanosis of Ito	semapv:ManualMappingCuration	2023-03-17
MONDO:0010305	creatine transporter deficiency	skos:exactMatch	DOID:0050800	cerebral creatine deficiency syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010306	X-linked intellectual disability, Cabezas type	skos:exactMatch	DOID:0060822	syndromic X-linked intellectual disability Cabezas type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010310	osteopathia striata with cranial sclerosis	skos:exactMatch	DOID:0060886	osteopathia striata with cranial sclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0010311	Becker muscular dystrophy	skos:exactMatch	DOID:9883	Becker muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010317	intellectual disability, X-linked, with or without seizures, arx-related	skos:exactMatch	DOID:0112021	non-syndromic X-linked intellectual disability ARX-related	semapv:ManualMappingCuration	2023-06-18
MONDO:0010319	syndromic X-linked intellectual disability Hedera type	skos:exactMatch	DOID:0060806	syndromic X-linked intellectual disability Hedera type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010320	retinitis pigmentosa 23	skos:exactMatch	DOID:0110412	retinitis pigmentosa 23	semapv:ManualMappingCuration	2024-04-21
MONDO:0010325	X-linked intellectual disability, Stocco dos Santos type	skos:exactMatch	DOID:0112126	Stocco Dos Santos type X-linked intellectual disability	semapv:ManualMappingCuration	2023-06-18
MONDO:0010327	HSD10 mitochondrial disease	skos:exactMatch	DOID:0060810	syndromic X-linked intellectual disability type 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0010328	alpha-thalassemia-myelodysplastic syndrome	skos:exactMatch	DOID:0112125	alpha-thalassemia myelodysplasia syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0010333	corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome	skos:exactMatch	DOID:0060816	corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010334	severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome	skos:exactMatch	DOID:0112123	deafness, dystonia, and cerebral hypomyelination	semapv:ManualMappingCuration	2023-04-17
MONDO:0010335	X-linked cone-rod dystrophy 3	skos:exactMatch	DOID:0111007	X-linked cone-rod dystrophy 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0010336	orofaciodigital syndrome VIII	skos:exactMatch	DOID:0060378	orofaciodigital syndrome VIII	semapv:ManualMappingCuration	2023-03-17
MONDO:0010337	X-linked intellectual disability-cerebellar hypoplasia syndrome	skos:exactMatch	DOID:0080311	X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance	semapv:ManualMappingCuration	2023-03-17
MONDO:0010338	X-linked distal spinal muscular atrophy type 3	skos:exactMatch	DOID:0111196	X-linked distal spinal muscular atrophy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0010339	epilepsy, X-linked 1, with variable learning disabilities and behavior disorders	skos:exactMatch	DOID:0112122	X-linked epilepsy with variable learning disabilities and behavior disorders	semapv:ManualMappingCuration	2023-04-17
MONDO:0010353	deafness-intellectual disability, Martin-Probst type syndrome	skos:exactMatch	DOID:0060830	deafness-intellectual disability, Martin-Probst type syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010354	Allan-Herndon-Dudley syndrome	skos:exactMatch	DOID:0050631	Allan-Herndon-Dudley syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010355	syndromic X-linked intellectual disability Claes-Jensen type	skos:exactMatch	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010356	nephrogenic syndrome of inappropriate antidiuresis	skos:exactMatch	DOID:0112121	nephrogenic syndrome of inappropriate antidiuresis	semapv:ManualMappingCuration	2023-03-17
MONDO:0010358	hypophosphatemic rickets, X-linked recessive	skos:exactMatch	DOID:0080353	X-linked recessive hypophosphatemic rickets	semapv:ManualMappingCuration	2024-04-21
MONDO:0010359	Dent disease type 2	skos:exactMatch	DOID:0081454	Dent disease 2	semapv:ManualMappingCuration	2024-07-21
MONDO:0010362	glycogen storage disease IXd	skos:exactMatch	DOID:0111040	glycogen storage disease IXD	semapv:ManualMappingCuration	2023-03-17
MONDO:0010367	SHOX-related short stature	skos:exactMatch	DOID:0112120	SHOX-related short stature	semapv:ManualMappingCuration	2023-03-17
MONDO:0010371	Aland island eye disease	skos:exactMatch	DOID:0050630	Aland Island eye disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010375	developmental and epileptic encephalopathy, 8	skos:exactMatch	DOID:0080215	developmental and epileptic encephalopathy 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0010378	X-linked hereditary sensory and autonomic neuropathy with hearing loss	skos:exactMatch	DOID:0111741	X-linked deafness 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0010379	Brunner syndrome	skos:exactMatch	DOID:0060693	Brunner syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010382	fragile X-associated tremor/ataxia syndrome	skos:exactMatch	DOID:0050879	fragile X-associated tremor/ataxia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010383	fragile X syndrome	skos:exactMatch	DOID:14261	fragile X syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010386	immunodeficiency 33	skos:exactMatch	DOID:0112003	immunodeficiency 33	semapv:ManualMappingCuration	2023-03-17
MONDO:0010389	X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency	skos:exactMatch	DOID:0112000	immunodeficiency 34	semapv:ManualMappingCuration	2023-04-17
MONDO:0010392	glycogen storage disease due to phosphoglycerate kinase 1 deficiency	skos:exactMatch	DOID:0111933	phosphoglycerate kinase 1 deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0010393	intellectual disability, X-linked 93	skos:exactMatch	DOID:0112045	non-syndromic X-linked intellectual disability 93	semapv:ManualMappingCuration	2023-06-18
MONDO:0010395	phosphoribosylpyrophosphate synthetase superactivity	skos:exactMatch	DOID:0111260	phosphoribosylpyrophosphate synthetase superactivity	semapv:ManualMappingCuration	2023-03-17
MONDO:0010396	developmental and epileptic encephalopathy, 2	skos:exactMatch	DOID:0080467	developmental and epileptic encephalopathy 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0010397	severe neonatal-onset encephalopathy with microcephaly	skos:exactMatch	DOID:0111932	severe congenital encephalopathy due to MECP2 mutation	semapv:ManualMappingCuration	2023-04-17
MONDO:0010399	chromosome Xp21 deletion syndrome	skos:exactMatch	DOID:0060427	chromosome Xp21 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010401	X-linked myopathy with postural muscle atrophy	skos:exactMatch	DOID:0070251	X-linked Emery-Dreifuss muscular dystrophy 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0010402	syndromic X-linked intellectual disability 94	skos:exactMatch	DOID:0060823	syndromic X-linked intellectual disability 94	semapv:ManualMappingCuration	2023-11-19
MONDO:0010404	X-linked non progressive cerebellar ataxia	skos:exactMatch	DOID:0111833	X-linked spinocerebellar ataxia 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0010406	chromosome Xp11.22 duplication syndrome	skos:exactMatch	DOID:0112037	chromosome Xp11.22 duplication syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0010407	intellectual disability, X-linked syndromic, Turner type	skos:exactMatch	DOID:0060811	syndromic X-linked intellectual disability Turner type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010408	syndactyly-telecanthus-anogenital and renal malformations syndrome	skos:exactMatch	DOID:0111931	syndactyly-telecanthus-anogenital and renal malformations syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010409	syndromic X-linked intellectual disability Shrimpton type	skos:exactMatch	DOID:0060813	syndromic X-linked intellectual disability Shrimpton type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010417	syndromic X-linked intellectual disability Najm type	skos:exactMatch	DOID:0060807	syndromic X-linked intellectual disability Najm type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010418	hereditary spastic paraplegia 34	skos:exactMatch	DOID:0110785	hereditary spastic paraplegia 34	semapv:ManualMappingCuration	2023-03-17
MONDO:0010421	Bruton-type agammaglobulinemia	skos:exactMatch	DOID:14179	X-linked agammaglobulinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010425	Lisch epithelial corneal dystrophy	skos:exactMatch	DOID:0060450	Lisch epithelial corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010426	X-linked endothelial corneal dystrophy	skos:exactMatch	DOID:0060446	X-linked endothelial corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010427	syndromic X-linked intellectual disability Raymond type	skos:exactMatch	DOID:0060824	syndromic X-linked intellectual disability Raymond type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010428	chromosome Xp11.23-p11.22 duplication syndrome	skos:exactMatch	DOID:0060461	chromosome Xp11.23-p11.22 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010431	Joubert syndrome 10	skos:exactMatch	DOID:0110981	Joubert syndrome 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0010432	thrombophilia, X-linked, due to factor 9 defect	skos:exactMatch	DOID:0111899	X-linked thrombophilia due to factor IX defect	semapv:ManualMappingCuration	2023-04-17
MONDO:0010435	nystagmus 6, congenital, X-linked	skos:exactMatch	DOID:0111795	congenital nystagmus 6	semapv:ManualMappingCuration	2023-06-18
MONDO:0010437	severe X-linked mitochondrial encephalomyopathy	skos:exactMatch	DOID:0111502	combined oxidative phosphorylation deficiency 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0010441	CK syndrome	skos:exactMatch	DOID:0111898	CK syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010444	X-linked dyserythropoetic anemia with abnormal platelets and neutropenia	skos:exactMatch	DOID:0112156	X-linked dyserythropoietic anemia	semapv:ManualMappingCuration	2023-04-17
MONDO:0010447	intellectual disability, X-linked 19	skos:exactMatch	DOID:0112019	non-syndromic X-linked intellectual disability 19	semapv:ManualMappingCuration	2024-04-21
MONDO:0010455	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia	skos:exactMatch	DOID:0080319	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010457	Ogden syndrome	skos:exactMatch	DOID:0050781	Ogden syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010459	amyotrophic lateral sclerosis type 15	skos:exactMatch	DOID:0060206	amyotrophic lateral sclerosis type 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0010460	syndromic X-linked intellectual disability 17	skos:exactMatch	DOID:0060803	syndromic X-linked intellectual disability 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0010461	syndromic X-linked intellectual disability Nascimento type	skos:exactMatch	DOID:0060820	syndromic X-linked intellectual disability Nascimento type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010463	X-linked dominant chondrodysplasia, Chassaing-Lacombe type	skos:exactMatch	DOID:0112106	chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia	semapv:ManualMappingCuration	2023-04-17
MONDO:0010466	multiple congenital anomalies-hypotonia-seizures syndrome 2	skos:exactMatch	DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0010472	developmental and epileptic encephalopathy, 36	skos:exactMatch	DOID:0080470	developmental and epileptic encephalopathy 36	semapv:ManualMappingCuration	2023-03-17
MONDO:0010473	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome	skos:exactMatch	DOID:0060828	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010475	X-linked central congenital hypothyroidism with late-onset testicular enlargement	skos:exactMatch	DOID:0111140	IGSF1 deficiency syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010476	neurodegeneration with brain iron accumulation 5	skos:exactMatch	DOID:0110739	neurodegeneration with brain iron accumulation 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0010478	SLC35A2-congenital disorder of glycosylation	skos:exactMatch	DOID:0070265	congenital disorder of glycosylation type IIm	semapv:ManualMappingCuration	2023-03-17
MONDO:0010479	Charcot-Marie-Tooth disease X-linked dominant 6	skos:exactMatch	DOID:0110207	Charcot-Marie-Tooth disease X-linked dominant 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0010482	X-linked parkinsonism-spasticity syndrome	skos:exactMatch	DOID:0112105	X-linked parkinsonism-spasticity syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010483	X-linked intellectual disability, Cantagrel type	skos:exactMatch	DOID:0112044	non-syndromic X-linked intellectual disability 98	semapv:ManualMappingCuration	2023-06-18
MONDO:0010485	X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome	skos:exactMatch	DOID:0111811	syndromic microphthalmia 13	semapv:ManualMappingCuration	2023-11-19
MONDO:0010487	intellectual disability, X-linked 99	skos:exactMatch	DOID:0112026	non-syndromic X-linked intellectual disability 99	semapv:ManualMappingCuration	2024-04-21
MONDO:0010490	SSR4-congenital disorder of glycosylation	skos:exactMatch	DOID:0080574	congenital disorder of glycosylation Iy	semapv:ManualMappingCuration	2023-04-17
MONDO:0010498	MEND syndrome	skos:exactMatch	DOID:0111865	MEND syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010501	syndromic X-linked intellectual disability 34	skos:exactMatch	DOID:0060817	syndromic X-linked intellectual disability 34	semapv:ManualMappingCuration	2023-11-19
MONDO:0010502	intellectual disability, X-linked 99, syndromic, female-restricted	skos:exactMatch	DOID:0112025	female-restricted syndromic X-linked intellectual disability 99	semapv:ManualMappingCuration	2023-11-19
MONDO:0010504	immunodeficiency 47	skos:exactMatch	DOID:0112002	immunodeficiency 47	semapv:ManualMappingCuration	2023-03-17
MONDO:0010512	intellectual disability, X-linked, syndromic, Bain type	skos:exactMatch	DOID:0070538	syndromic X-linked intellectual developmental disorder Bain type	semapv:ManualMappingCuration	2024-04-21
MONDO:0010514	combined immunodeficiency due to moesin deficiency	skos:exactMatch	DOID:0112001	immunodeficiency 50	semapv:ManualMappingCuration	2023-11-19
MONDO:0010518	Wiskott-Aldrich syndrome	skos:exactMatch	DOID:9169	Wiskott-Aldrich syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010519	alpha thalassemia-X-linked intellectual disability syndrome	skos:exactMatch	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010520	X-linked Alport syndrome	skos:exactMatch	DOID:0110034	X-linked Alport syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010523	X-linked reticulate pigmentary disorder	skos:exactMatch	DOID:0111834	X-linked reticulate pigmentary disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0010524	X-linked sideroblastic anemia with ataxia	skos:exactMatch	DOID:0050554	X-linked sideroblastic anemia with ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010526	Fabry disease	skos:exactMatch	DOID:14499	Fabry disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010529	X-linked spinocerebellar ataxia type 3	skos:exactMatch	DOID:0111831	X-linked spinocerebellar ataxia 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0010532	infantile-onset X-linked spinal muscular atrophy	skos:exactMatch	DOID:0111827	X-linked spinal muscular atrophy 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0010533	Arts syndrome	skos:exactMatch	DOID:0050647	Arts syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010534	X-linked spinocerebellar ataxia type 4	skos:exactMatch	DOID:0111832	X-linked spinocerebellar ataxia 4	semapv:ManualMappingCuration	2023-04-17
MONDO:0010537	Borjeson-Forssman-Lehmann syndrome	skos:exactMatch	DOID:0050681	Borjeson-Forssman-Lehmann syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010538	Mononen-Karnes-Senac syndrome	skos:exactMatch	DOID:0110973	Mononen-Karnes-Senac syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010542	dilated cardiomyopathy 3B	skos:exactMatch	DOID:0081164	dilated cardiomyopathy 3B	semapv:ManualMappingCuration	2024-02-18
MONDO:0010542	dilated cardiomyopathy 3B	skos:exactMatch	DOID:0110461	X-linked dilated cardiomyopathy	semapv:ManualMappingCuration	2024-02-18
MONDO:0010543	Barth syndrome	skos:exactMatch	DOID:0050476	Barth syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010544	cataract 40	skos:exactMatch	DOID:0110272	cataract 40	semapv:ManualMappingCuration	2024-04-21
MONDO:0010545	Nance-Horan syndrome	skos:exactMatch	DOID:0060599	Nance-Horan syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010547	X-linked progressive cerebellar ataxia	skos:exactMatch	DOID:0111829	X-linked spinocerebellar ataxia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0010549	Charcot-Marie-Tooth disease X-linked dominant 1	skos:exactMatch	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010550	Charcot-Marie-Tooth disease X-linked recessive 2	skos:exactMatch	DOID:0110208	Charcot-Marie-Tooth disease X-linked recessive 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0010551	Charcot-Marie-Tooth disease X-linked recessive 3	skos:exactMatch	DOID:0110211	Charcot-Marie-Tooth disease X-linked recessive 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0010554	Abruzzo-Erickson syndrome	skos:exactMatch	DOID:0111826	Abruzzo-Erickson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010556	X-linked chondrodysplasia punctata	skos:exactMatch	DOID:0060292	X-linked chondrodysplasia punctata 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010557	choroideremia	skos:exactMatch	DOID:9821	Choroideremia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010559	MASA syndrome	skos:exactMatch	DOID:0060246	MASA syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010560	cleft palate with or without ankyloglossia, X-linked	skos:exactMatch	DOID:0060613	X-linked cleft palate with or without ankyloglossia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010561	Coffin-Lowry syndrome	skos:exactMatch	DOID:3783	Coffin-Lowry syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010563	blue cone monochromacy	skos:exactMatch	DOID:0050679	blue cone monochromacy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010566	X-linked cone-rod dystrophy 1	skos:exactMatch	DOID:0111008	X-linked cone-rod dystrophy 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0010568	Aicardi syndrome	skos:exactMatch	DOID:8461	Aicardi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010570	craniofrontonasal syndrome	skos:exactMatch	DOID:14737	craniofrontonasal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010571	otopalatodigital syndrome type 2	skos:exactMatch	DOID:0111784	otopalatodigital syndrome type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0010572	occipital horn syndrome	skos:exactMatch	DOID:0111272	occipital horn syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010574	syndromic X-linked intellectual disability 5	skos:exactMatch	DOID:0060800	syndromic X-linked intellectual disability 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0010576	X-linked mixed hearing loss with perilymphatic gusher	skos:exactMatch	DOID:0111737	X-linked deafness 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0010578	deafness dystonia syndrome	skos:exactMatch	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010580	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome	skos:exactMatch	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010584	dyskeratosis congenita, X-linked	skos:exactMatch	DOID:0070025	X-linked dyskeratosis congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0010585	X-linked hypohidrotic ectodermal dysplasia	skos:exactMatch	DOID:0111664	ectodermal dysplasia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0010588	exudative vitreoretinopathy 2, X-linked	skos:exactMatch	DOID:0111413	X-linked exudative vitreoretinopathy 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0010589	Aarskog-Scott syndrome, X-linked	skos:exactMatch	DOID:6683	X-linked Aarskog syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0010592	focal dermal hypoplasia	skos:exactMatch	DOID:2120	focal dermal hypoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010598	glycogen storage disease IXa1	skos:exactMatch	DOID:0111042	glycogen storage disease IXA	semapv:ManualMappingCuration	2023-11-19
MONDO:0010598	glycogen storage disease IXa1	skos:exactMatch	DOID:2751	glycogen storage disease VIII	semapv:ManualMappingCuration	2023-11-19
MONDO:0010602	hemophilia A	skos:exactMatch	DOID:12134	factor VIII deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010604	hemophilia B	skos:exactMatch	DOID:12259	hemophilia B	semapv:ManualMappingCuration	2023-03-17
MONDO:0010613	inborn glycerol kinase deficiency	skos:exactMatch	DOID:0060363	glycerol kinase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010615	isolated growth hormone deficiency type III	skos:exactMatch	DOID:0060875	isolated growth hormone deficiency type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0010618	familial isolated hypoparathyroidism due to agenesis of parathyroid gland	skos:exactMatch	DOID:0111388	X-linked hypoparathyroidism	semapv:ManualMappingCuration	2023-04-17
MONDO:0010619	X-linked dominant hypophosphatemic rickets	skos:exactMatch	DOID:0050445	X-linked dominant hypophosphatemic rickets	semapv:ManualMappingCuration	2023-03-17
MONDO:0010621	CHILD syndrome	skos:exactMatch	DOID:0111822	CHILD syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010622	recessive X-linked ichthyosis	skos:exactMatch	DOID:1700	X-linked ichthyosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0010626	hyper-IgM syndrome type 1	skos:exactMatch	DOID:0060022	CD40 ligand deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010626	hyper-IgM syndrome type 1	skos:exactMatch	DOID:6620	X-linked hyper IgM syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010627	X-linked lymphoproliferative syndrome	skos:exactMatch	DOID:0060705	X-linked lymphoproliferative syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010631	incontinentia pigmenti	skos:exactMatch	DOID:12305	Bloch-Sulzberger syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010632	developmental and epileptic encephalopathy, 1	skos:exactMatch	DOID:0080468	developmental and epileptic encephalopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010635	hypogonadotropic hypogonadism 1 with or without anosmia	skos:exactMatch	DOID:0090094	hypogonadotropic hypogonadism 1 with or without anosmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010645	oculocerebrorenal syndrome	skos:exactMatch	DOID:1056	oculocerebrorenal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010647	spermatogenic failure, X-linked, 2	skos:exactMatch	DOID:0070185	X-linked spermatogenic failure 2	semapv:ManualMappingCuration	2024-02-18
MONDO:0010650	Melnick-Needles syndrome	skos:exactMatch	DOID:0111788	Melnick-Needles syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010651	Menkes disease	skos:exactMatch	DOID:1838	Menkes disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010653	Renpenning syndrome	skos:exactMatch	DOID:0060179	Renpenning syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010654	Partington syndrome	skos:exactMatch	DOID:14744	Partington syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010655	X-linked intellectual disability with marfanoid habitus	skos:exactMatch	DOID:0080985	syndromic X-linked intellectual disorder Lujan-Fryns-type	semapv:ManualMappingCuration	2023-06-18
MONDO:0010657	methylmalonic acidemia with homocystinuria, type cblX	skos:exactMatch	DOID:0111814	methylmalonic acidemia and homocysteinemia cblX type	semapv:ManualMappingCuration	2023-04-17
MONDO:0010658	syndromic X-linked intellectual disability 12	skos:exactMatch	DOID:0060804	syndromic X-linked intellectual disability 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0010659	FRAXE intellectual disability	skos:exactMatch	DOID:0080984	X-linked intellectual developmental disorder 109	semapv:ManualMappingCuration	2023-06-18
MONDO:0010661	severe X-linked intellectual disability, Gustavson type	skos:exactMatch	DOID:0081123	X-linked mental retardation Gustavson type	semapv:ManualMappingCuration	2023-06-18
MONDO:0010663	intellectual disability-hypotonic facies syndrome, X-linked, 1	skos:exactMatch	DOID:0080982	X-linked mental retardation-hypotonic facies syndrome-1	semapv:ManualMappingCuration	2023-06-18
MONDO:0010664	syndromic X-linked intellectual disability Snyder type	skos:exactMatch	DOID:0060802	syndromic X-linked intellectual disability Snyder type	semapv:ManualMappingCuration	2023-03-17
MONDO:0010665	Wilson-Turner syndrome	skos:exactMatch	DOID:0060814	Wilson-Turner syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010667	Prieto syndrome	skos:exactMatch	DOID:0060805	Prieto syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010669	syndactyly type 8	skos:exactMatch	DOID:0111813	syndactyly type 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0010672	linear skin defects with multiple congenital anomalies	skos:exactMatch	DOID:0111875	MLS syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0010674	mucopolysaccharidosis type 2	skos:exactMatch	DOID:12799	mucopolysaccharidosis II	semapv:ManualMappingCuration	2023-03-17
MONDO:0010679	Duchenne muscular dystrophy	skos:exactMatch	DOID:11723	Duchenne muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010683	X-linked myotubular myopathy	skos:exactMatch	DOID:0111225	centronuclear myopathy X-linked	semapv:ManualMappingCuration	2023-03-17
MONDO:0010684	X-linked myopathy with excessive autophagy	skos:exactMatch	DOID:0050760	X-linked myopathy with excessive autophagy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010686	N syndrome	skos:exactMatch	DOID:0050769	N syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010689	Charcot-Marie-Tooth disease X-linked recessive 4	skos:exactMatch	DOID:0110212	Charcot-Marie-Tooth disease X-linked recessive 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0010691	Norrie disease	skos:exactMatch	DOID:0060844	Norrie disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010693	nystagmus 1, congenital, X-linked	skos:exactMatch	DOID:0111790	congenital nystagmus 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0010698	optic atrophy 2	skos:exactMatch	DOID:0111443	optic atrophy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0010699	Charcot-Marie-Tooth disease X-linked recessive 5	skos:exactMatch	DOID:0110210	Charcot-Marie-Tooth disease X-linked recessive 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0010702	orofaciodigital syndrome I	skos:exactMatch	DOID:0060316	orofaciodigital syndrome I	semapv:ManualMappingCuration	2023-03-17
MONDO:0010704	otopalatodigital syndrome type 1	skos:exactMatch	DOID:0111783	otopalatodigital syndrome type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010706	premature ovarian failure 1	skos:exactMatch	DOID:0080857	primary ovarian insufficiency 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0010709	early-onset parkinsonism-intellectual disability syndrome	skos:exactMatch	DOID:0111781	Waisman syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010711	TARP syndrome	skos:exactMatch	DOID:0111780	TARP syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010713	properdin deficiency, X-linked	skos:exactMatch	DOID:0111768	X-linked properdin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010714	Pelizeaus-Merzbacher spectrum disorder	skos:exactMatch	DOID:3210	Pelizaeus-Merzbacher disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010720	partial androgen insensitivity syndrome	skos:exactMatch	DOID:0080776	partial androgen insensitivity syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010725	X-linked retinoschisis	skos:exactMatch	DOID:0060763	X-linked juvenile retinoschisis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010726	Rett syndrome	skos:exactMatch	DOID:1206	Rett syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010732	spastic paraparesis-deafness syndrome	skos:exactMatch	DOID:0081100	spastic paraplegia with deafness	semapv:ManualMappingCuration	2023-04-17
MONDO:0010733	hereditary spastic paraplegia 2	skos:exactMatch	DOID:0110773	hereditary spastic paraplegia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0010735	Kennedy disease	skos:exactMatch	DOID:0060161	Kennedy's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0010737	spondyloepiphyseal dysplasia tarda, X-linked	skos:exactMatch	DOID:0080362	X-linked spondyloepiphyseal dysplasia tarda	semapv:ManualMappingCuration	2023-11-19
MONDO:0010745	beta-thalassemia-X-linked thrombocytopenia syndrome	skos:exactMatch	DOID:0111767	X-linked thrombocytopenia with beta-thalassemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010747	X-linked dystonia-parkinsonism	skos:exactMatch	DOID:0090057	X-linked dystonia-parkinsonism	semapv:ManualMappingCuration	2023-03-17
MONDO:0010752	VACTERL association, X-linked, with or without hydrocephalus	skos:exactMatch	DOID:0111766	X-linked VACTERL association	semapv:ManualMappingCuration	2023-03-17
MONDO:0010753	cardiac valvular dysplasia, X-linked	skos:exactMatch	DOID:0111765	X-linked cardiac valvular dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010758	Wieacker-Wolff syndrome	skos:exactMatch	DOID:0060815	Miles-Carpenter syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010765	46,XY complete gonadal dysgenesis	skos:exactMatch	DOID:14448	46,XY sex reversal	semapv:ManualMappingCuration	2023-03-17
MONDO:0010768	gonadoblastoma	skos:exactMatch	DOID:3301	gonadoblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0010771	histiocytoid cardiomyopathy	skos:exactMatch	DOID:0080198	infantile histiocytoid cardiomyopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010779	mitochondrial non-syndromic sensorineural hearing loss	skos:exactMatch	DOID:0111751	mitochondrial nonsyndromic sensorineural deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0010787	Kearns-Sayre syndrome	skos:exactMatch	DOID:12934	Kearns-Sayre syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010788	Leber hereditary optic neuropathy	skos:exactMatch	DOID:705	Leber hereditary optic neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010789	MELAS syndrome	skos:exactMatch	DOID:3687	MELAS syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010790	MERRF syndrome	skos:exactMatch	DOID:310	MERRF Syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010794	NARP syndrome	skos:exactMatch	DOID:0111273	NARP syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010797	Pearson syndrome	skos:exactMatch	DOID:0060067	Pearson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010799	deafness, aminoglycoside-induced	skos:exactMatch	DOID:0111734	aminoglycoside-induced deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0010802	pancreatic hypoplasia-diabetes-congenital heart disease syndrome	skos:exactMatch	DOID:0111733	pancreatic hypoplasia-diabetes-congenital heart disease syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010803	Eiken syndrome	skos:exactMatch	DOID:0111732	Eiken syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010805	bladder exstrophy	skos:exactMatch	DOID:0080174	bladder exstrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010807	autosomal recessive nonsyndromic hearing loss 2	skos:exactMatch	DOID:0110477	autosomal recessive nonsyndromic deafness 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0010808	fatal familial insomnia	skos:exactMatch	DOID:0050433	fatal familial insomnia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010814	chondrodysplasia-pseudohermaphroditism syndrome	skos:exactMatch	DOID:0060644	chondrodysplasia-pseudohermaphroditism syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010816	Qazi Markouizos syndrome	skos:exactMatch	DOID:0050740	Qazi Markouizos syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010817	autosomal dominant nonsyndromic hearing loss 2A	skos:exactMatch	DOID:0110558	autosomal dominant nonsyndromic deafness 2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0010818	retinitis pigmentosa 12	skos:exactMatch	DOID:0110358	retinitis pigmentosa 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0010823	rhizomelic chondrodysplasia punctata type 3	skos:exactMatch	DOID:0110853	rhizomelic chondrodysplasia punctata type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0010826	childhood absence epilepsy	skos:exactMatch	DOID:0050708	early onset absence epilepsy	semapv:ManualMappingCuration	2024-06-23
MONDO:0010826	childhood absence epilepsy	skos:exactMatch	DOID:1825	childhood absence epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010830	neuronal ceroid lipofuscinosis 8	skos:exactMatch	DOID:0110723	neuronal ceroid lipofuscinosis 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0010839	neuronopathy, distal hereditary motor, autosomal dominant 8	skos:exactMatch	DOID:0111215	autosomal dominant distal hereditary motor neuronopathy 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0010842	multiple cutaneous and mucosal venous malformations	skos:exactMatch	DOID:0050792	multiple cutaneous and mucosal venous malformations	semapv:ManualMappingCuration	2023-03-17
MONDO:0010847	spinocerebellar ataxia type 4	skos:exactMatch	DOID:0050957	spinocerebellar ataxia type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0010848	spinocerebellar ataxia type 5	skos:exactMatch	DOID:0050882	spinocerebellar ataxia type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0010850	Tessier number 4 facial cleft	skos:exactMatch	DOID:0111706	oblique facial clefting 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0010854	Toriello-Lacassie-Droste syndrome	skos:exactMatch	DOID:0111705	oculoectodermal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010857	semantic dementia	skos:exactMatch	DOID:0081391	semantic dementia	semapv:ManualMappingCuration	2024-04-21
MONDO:0010863	type 1 diabetes mellitus 5	skos:exactMatch	DOID:0110744	type 1 diabetes mellitus 5	semapv:ManualMappingCuration	2023-11-19
MONDO:0010866	infantile osteopetrosis with neuroaxonal dysplasia	skos:exactMatch	DOID:0070343	CSF1R-related brain malformation and osteopetrosis	semapv:ManualMappingCuration	2023-04-17
MONDO:0010870	tibial muscular dystrophy	skos:exactMatch	DOID:0111078	tibial muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010877	Charcot-Marie-Tooth disease type 5	skos:exactMatch	DOID:0080067	Charcot-Marie-Tooth disease type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0010878	hereditary spastic paraplegia 6	skos:exactMatch	DOID:0110811	hereditary spastic paraplegia 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0010879	CODAS syndrome	skos:exactMatch	DOID:0111274	CODAS syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010886	2q37 microdeletion syndrome	skos:exactMatch	DOID:0111704	chromosome 2q37 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010888	adenomyosis	skos:exactMatch	DOID:288	endometriosis of uterus	semapv:ManualMappingCuration	2023-03-17
MONDO:0010890	acrocardiofacial syndrome	skos:exactMatch	DOID:0070419	acrocardiofacial syndrome	semapv:ManualMappingCuration	2023-07-09
MONDO:0010894	maturity-onset diabetes of the young type 3	skos:exactMatch	DOID:0111102	maturity-onset diabetes of the young type 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0010895	ABCD syndrome	skos:exactMatch	DOID:0050600	ABCD syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010896	pigment dispersion syndrome	skos:exactMatch	DOID:0060680	pigment dispersion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010898	autosomal dominant epilepsy with auditory features	skos:exactMatch	DOID:0060748	familial temporal lobe epilepsy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0010906	orofacial cleft 11	skos:exactMatch	DOID:0080404	orofacial cleft 11	semapv:ManualMappingCuration	2023-11-19
MONDO:0010907	familial hypertryptophanemia	skos:exactMatch	DOID:0111703	familial hypertryptophanemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0010908	loose anagen syndrome	skos:exactMatch	DOID:0111702	loose anagen hair syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010912	fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement	skos:exactMatch	DOID:0081017	congenital fibrosis of the extraocular muscles 3A	semapv:ManualMappingCuration	2024-04-21
MONDO:0010915	autosomal dominant nonsyndromic hearing loss 4A	skos:exactMatch	DOID:0110573	autosomal dominant nonsyndromic deafness 4A	semapv:ManualMappingCuration	2024-04-21
MONDO:0010916	polycystic kidney disease 3 with or without polycystic liver disease	skos:exactMatch	DOID:0110860	polycystic kidney disease 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0010924	D-2-hydroxyglutaric aciduria	skos:exactMatch	DOID:0050575	D-2-hydroxyglutaric aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0010926	familial hypocalciuric hypercalcemia 3	skos:exactMatch	DOID:0060702	familial hypocalciuric hypercalcemia 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0010933	autosomal recessive nonsyndromic hearing loss 4	skos:exactMatch	DOID:0110498	autosomal recessive nonsyndromic deafness 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0010943	schizophrenia 4	skos:exactMatch	DOID:0070080	schizophrenia 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0010946	hypertrophic cardiomyopathy 6	skos:exactMatch	DOID:0110312	hypertrophic cardiomyopathy 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0010949	Charcot-Marie-Tooth disease type 2B	skos:exactMatch	DOID:0110159	Charcot-Marie-Tooth disease type 2B	semapv:ManualMappingCuration	2023-03-17
MONDO:0010952	hereditary hyperferritinemia with congenital cataracts	skos:exactMatch	DOID:0111256	hyperferritinemia-cataract syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010953	Fanconi anemia complementation group E	skos:exactMatch	DOID:0111084	Fanconi anemia complementation group E	semapv:ManualMappingCuration	2023-03-17
MONDO:0010959	van den Ende-Gupta syndrome	skos:exactMatch	DOID:0111699	Van den Ende-Gupta syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010961	obesity due to prohormone convertase I deficiency	skos:exactMatch	DOID:0111698	proprotein convertase 1/3 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0010962	diffuse nonepidermolytic palmoplantar keratoderma	skos:exactMatch	DOID:0050428	nonepidermolytic palmoplantar keratoderma	semapv:ManualMappingCuration	2023-11-19
MONDO:0010966	achondrogenesis type IB	skos:exactMatch	DOID:0080055	achondrogenesis type IB	semapv:ManualMappingCuration	2023-03-17
MONDO:0010967	autosomal recessive nonsyndromic hearing loss 7	skos:exactMatch	DOID:0110520	autosomal recessive nonsyndromic deafness 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0010970	cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies	skos:exactMatch	DOID:0111697	cleft palate, cardiac defects, and intellectual disabillity	semapv:ManualMappingCuration	2023-11-19
MONDO:0010977	Brody myopathy	skos:exactMatch	DOID:0050692	Brody myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0010979	Timothy syndrome	skos:exactMatch	DOID:0060173	Timothy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0010983	dystonia 9	skos:exactMatch	DOID:0090044	dystonia 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0010986	autosomal recessive nonsyndromic hearing loss 9	skos:exactMatch	DOID:0110535	autosomal recessive nonsyndromic deafness 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0010989	Mayer-Rokitansky-Küster-Hauser syndrome type 2	skos:exactMatch	DOID:0112179	Mayer-Rokitansky-Kuster-Hauser syndrome type 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0010995	Charcot-Marie-Tooth disease type 1C	skos:exactMatch	DOID:0110151	Charcot-Marie-Tooth disease type 1C	semapv:ManualMappingCuration	2023-03-17
MONDO:0010998	ALG3-congenital disorder of glycosylation	skos:exactMatch	DOID:0080556	congenital disorder of glycosylation Id	semapv:ManualMappingCuration	2023-03-17
MONDO:0011001	Brugada syndrome 1	skos:exactMatch	DOID:0110218	Brugada syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0011003	dilated cardiomyopathy 1E	skos:exactMatch	DOID:0110433	dilated cardiomyopathy 1E	semapv:ManualMappingCuration	2024-02-18
MONDO:0011010	Matthew-Wood syndrome	skos:exactMatch	DOID:0111807	syndromic microphthalmia 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0011012	African iron overload	skos:exactMatch	DOID:0111033	African iron overload	semapv:ManualMappingCuration	2023-03-17
MONDO:0011013	autosomal dominant hypocalcemia 1	skos:exactMatch	DOID:0090107	autosomal dominant hypocalcemia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011017	Naxos disease	skos:exactMatch	DOID:0080551	Naxos disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0011018	brachyolmia-amelogenesis imperfecta syndrome	skos:exactMatch	DOID:0090143	brachyolmia-amelogenesis imperfecta syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011022	Potocki-Shaffer syndrome	skos:exactMatch	DOID:0111687	Potocki-Shaffer syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011023	hereditary mixed polyposis syndrome	skos:exactMatch	DOID:0111684	hereditary mixed polyposis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011025	Cayman type cerebellar ataxia	skos:exactMatch	DOID:0060694	Cayman type cerebellar ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011026	autosomal recessive congenital ichthyosis 4A	skos:exactMatch	DOID:0060712	autosomal recessive congenital ichthyosis 4A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011028	autosomal recessive limb-girdle muscular dystrophy type 2F	skos:exactMatch	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F	semapv:ManualMappingCuration	2023-03-17
MONDO:0011031	autosomal dominant nonsyndromic hearing loss 10	skos:exactMatch	DOID:0110542	autosomal dominant nonsyndromic deafness 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0011032	autosomal dominant nonsyndromic hearing loss 11	skos:exactMatch	DOID:0110543	autosomal dominant nonsyndromic deafness 11	semapv:ManualMappingCuration	2024-04-21
MONDO:0011035	neurofibromatosis-Noonan syndrome	skos:exactMatch	DOID:0111683	neurofibromatosis-Noonan syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011045	MMEP syndrome	skos:exactMatch	DOID:0111803	syndromic microphthalmia 8	semapv:ManualMappingCuration	2023-04-17
MONDO:0011053	intellectual disability-sparse hair-brachydactyly syndrome	skos:exactMatch	DOID:0081441	Nicolaides-Baraitser syndrome	semapv:ManualMappingCuration	2024-05-19
MONDO:0011066	Charcot-Marie-Tooth disease type 4B1	skos:exactMatch	DOID:0110191	Charcot-Marie-Tooth disease type 4B1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011068	type 1 diabetes mellitus 12	skos:exactMatch	DOID:0110751	type 1 diabetes mellitus 12	semapv:ManualMappingCuration	2023-11-19
MONDO:0011070	van Maldergem syndrome 1	skos:exactMatch	DOID:0080585	Van Maldergem syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0011074	autosomal dominant nonsyndromic hearing loss 7	skos:exactMatch	DOID:0110591	autosomal dominant nonsyndromic deafness 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0011076	myofibrillar myopathy 1	skos:exactMatch	DOID:0080092	myofibrillar myopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011085	Charcot-Marie-Tooth disease type 4D	skos:exactMatch	DOID:0110186	Charcot-Marie-Tooth disease type 4D	semapv:ManualMappingCuration	2023-03-17
MONDO:0011086	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive	skos:exactMatch	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive	semapv:ManualMappingCuration	2023-03-17
MONDO:0011091	Charcot-Marie-Tooth disease type 2D	skos:exactMatch	DOID:0110164	Charcot-Marie-Tooth disease type 2D	semapv:ManualMappingCuration	2023-03-17
MONDO:0011093	mucopolysaccharidosis type 9	skos:exactMatch	DOID:0050809	mucopolysaccharidosis IX	semapv:ManualMappingCuration	2023-03-17
MONDO:0011099	human HOXA1 syndromes	skos:exactMatch	DOID:0050682	Athabaskan brainstem dysgenesis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011101	peroxisome biogenesis disorder 1B	skos:exactMatch	DOID:0081240	peroxisome biogenesis disorder 1B	semapv:ManualMappingCuration	2023-03-17
MONDO:0011103	autosomal dominant nonsyndromic hearing loss 3A	skos:exactMatch	DOID:0110564	autosomal dominant nonsyndromic deafness 3A	semapv:ManualMappingCuration	2024-04-21
MONDO:0011107	congenital hypotrichosis with juvenile macular dystrophy	skos:exactMatch	DOID:0110711	congenital hypotrichosis with juvenile macular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011113	Charcot-Marie-Tooth disease type 4C	skos:exactMatch	DOID:0110183	Charcot-Marie-Tooth disease type 4C	semapv:ManualMappingCuration	2023-03-17
MONDO:0011119	iridogoniodysgenesis	skos:exactMatch	DOID:0050786	iridogoniodysgenesis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011125	trichothiodystrophy 1, photosensitive	skos:exactMatch	DOID:0111873	photosensitive trichothiodystrophy 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0011128	Sheldon-hall syndrome	skos:exactMatch	DOID:0111599	distal arthrogryposis type 2B	semapv:ManualMappingCuration	2023-03-17
MONDO:0011132	T-cell immunodeficiency, congenital alopecia, and nail dystrophy	skos:exactMatch	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011136	Quebec platelet disorder	skos:exactMatch	DOID:0111050	Quebec platelet disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0011137	retinitis pigmentosa 19	skos:exactMatch	DOID:0110354	retinitis pigmentosa 19	semapv:ManualMappingCuration	2024-04-21
MONDO:0011143	cone-rod dystrophy 6	skos:exactMatch	DOID:0111011	cone-rod dystrophy 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0011144	ceroid lipofuscinosis, neuronal, 6A	skos:exactMatch	DOID:0110729	neuronal ceroid lipofuscinosis 6A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011147	chromosome 18q deletion syndrome	skos:exactMatch	DOID:0060407	chromosome 18q deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011152	PHGDH deficiency	skos:exactMatch	DOID:0050722	PHGDH deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0011153	hyperinsulinemic hypoglycemia, familial, 2	skos:exactMatch	DOID:0070218	familial hyperinsulinemic hypoglycemia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011154	acrofacial dysostosis, Palagonia type	skos:exactMatch	DOID:0060385	acrofacial dysostosis, Patagonia type	semapv:ManualMappingCuration	2023-03-17
MONDO:0011156	progressive familial intrahepatic cholestasis type 2	skos:exactMatch	DOID:0070222	progressive familial intrahepatic cholestasis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011159	autosomal dominant nonsyndromic hearing loss 13	skos:exactMatch	DOID:0110545	autosomal dominant nonsyndromic deafness 13	semapv:ManualMappingCuration	2024-04-21
MONDO:0011168	type 1 diabetes mellitus 10	skos:exactMatch	DOID:0110749	type 1 diabetes mellitus 10	semapv:ManualMappingCuration	2023-11-19
MONDO:0011170	autosomal recessive limb-girdle muscular dystrophy type 2G	skos:exactMatch	DOID:0110281	autosomal recessive limb-girdle muscular dystrophy type 2G	semapv:ManualMappingCuration	2023-03-17
MONDO:0011176	intestinal hypomagnesemia 1	skos:exactMatch	DOID:0060883	intestinal hypomagnesemia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011184	childhood apraxia of speech	skos:exactMatch	DOID:0111275	speech-language disorder-1	semapv:ManualMappingCuration	2023-04-17
MONDO:0011185	Thiel-Behnke corneal dystrophy	skos:exactMatch	DOID:0060455	Thiel-Behnke corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011190	nephronophthisis 2	skos:exactMatch	DOID:0111113	nephronophthisis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011192	autosomal recessive nonsyndromic hearing loss 18A	skos:exactMatch	DOID:0110473	autosomal recessive nonsyndromic deafness 18A	semapv:ManualMappingCuration	2024-04-21
MONDO:0011193	cone dystrophy 3	skos:exactMatch	DOID:0080314	cone-rod dystrophy 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0011196	amyotrophic lateral sclerosis type 5	skos:exactMatch	DOID:0060197	amyotrophic lateral sclerosis type 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0011198	spondyloepimetaphyseal dysplasia, Missouri type	skos:exactMatch	DOID:0080030	spondyloepimetaphyseal dysplasia, Missouri type	semapv:ManualMappingCuration	2023-03-17
MONDO:0011200	torsion dystonia 7	skos:exactMatch	DOID:0090040	torsion dystonia 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0011211	axial spondylometaphyseal dysplasia	skos:exactMatch	DOID:0112299	axial spondylometaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011213	Pierpont syndrome	skos:exactMatch	DOID:0081362	Pierpont syndrome	semapv:ManualMappingCuration	2023-07-09
MONDO:0011214	progressive familial intrahepatic cholestasis type 3	skos:exactMatch	DOID:0070223	progressive familial intrahepatic cholestasis 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011216	hemochromatosis type 2A	skos:exactMatch	DOID:0111027	hemochromatosis type 2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011218	autosomal recessive congenital ichthyosis 11	skos:exactMatch	DOID:0060720	autosomal recessive congenital ichthyosis 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0011219	Fried's tooth and nail syndrome	skos:exactMatch	DOID:0111661	ectodermal dysplasia 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0011223	amyotrophic lateral sclerosis type 4	skos:exactMatch	DOID:0060196	amyotrophic lateral sclerosis type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0011225	severe combined immunodeficiency due to DCLRE1C deficiency	skos:exactMatch	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation	semapv:ManualMappingCuration	2023-03-17
MONDO:0011229	ethylmalonic encephalopathy	skos:exactMatch	DOID:0060640	ethylmalonic encephalopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011231	febrile seizures, familial, 2	skos:exactMatch	DOID:0111310	familial febrile seizures 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011236	hyperinsulinism due to glucokinase deficiency	skos:exactMatch	DOID:0070216	familial hyperinsulinemic hypoglycemia 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011242	Bartter disease type 4A	skos:exactMatch	DOID:0110145	Bartter disease type 4A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011244	Marshall-Smith syndrome	skos:exactMatch	DOID:0050858	Marshall-Smith syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011246	megaconial type congenital muscular dystrophy	skos:exactMatch	DOID:0110632	megaconial type congenital muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011257	MPI-congenital disorder of glycosylation	skos:exactMatch	DOID:0080554	congenital disorder of glycosylation Ib	semapv:ManualMappingCuration	2023-03-17
MONDO:0011261	spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability	skos:exactMatch	DOID:0112294	spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability	semapv:ManualMappingCuration	2023-03-17
MONDO:0011264	torsion dystonia 6	skos:exactMatch	DOID:0090039	torsion dystonia 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0011266	myotonic dystrophy type 2	skos:exactMatch	DOID:0050759	myotonic dystrophy type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011269	psoriasis 2	skos:exactMatch	DOID:0080475	psoriasis 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0011271	rigid spine muscular dystrophy 1	skos:exactMatch	DOID:0110633	rigid spine muscular dystrophy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011273	H syndrome	skos:exactMatch	DOID:0111278	histiocytosis-lymphadenopathy plus syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0011274	Muenke syndrome	skos:exactMatch	DOID:0060703	Muenke syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011275	acromesomelic dysplasia 1, Maroteaux type	skos:exactMatch	DOID:0080050	acromesomelic dysplasia, Maroteaux type	semapv:ManualMappingCuration	2023-03-17
MONDO:0011283	mitochondrial DNA depletion syndrome 1	skos:exactMatch	DOID:0080119	mitochondrial DNA depletion syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011291	ALG6-congenital disorder of glycosylation 1C	skos:exactMatch	DOID:0080555	congenital disorder of glycosylation Ic	semapv:ManualMappingCuration	2023-03-17
MONDO:0011299	Huntington disease-like 1	skos:exactMatch	DOID:0090103	Huntington's disease-like 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011301	pseudohypoparathyroidism type 1B	skos:exactMatch	DOID:0080222	pseudohypoparathyroidism type IB	semapv:ManualMappingCuration	2023-03-17
MONDO:0011302	type 1 diabetes mellitus 17	skos:exactMatch	DOID:0110754	type 1 diabetes mellitus 17	semapv:ManualMappingCuration	2023-11-19
MONDO:0011303	focal segmental glomerulosclerosis 1	skos:exactMatch	DOID:0111128	focal segmental glomerulosclerosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011308	GRACILE syndrome	skos:exactMatch	DOID:0111455	GRACILE syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011309	familial gestational hyperthyroidism	skos:exactMatch	DOID:0081102	familial gestational hyperthyroidism	semapv:ManualMappingCuration	2023-03-17
MONDO:0011327	neuronal intranuclear inclusion disease	skos:exactMatch	DOID:0081294	neuronal intranuclear inclusion disease	semapv:ManualMappingCuration	2023-04-17
MONDO:0011330	spinocerebellar ataxia type 10	skos:exactMatch	DOID:0050960	spinocerebellar ataxia type 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0011331	congenital chylothorax	skos:exactMatch	DOID:0060646	congenital chylothorax	semapv:ManualMappingCuration	2024-06-23
MONDO:0011335	spondyloepimetaphyseal dysplasia with multiple dislocations	skos:exactMatch	DOID:0112199	spondyloepimetaphyseal dysplasia with joint laxity type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011338	Omenn syndrome	skos:exactMatch	DOID:0060010	Omenn syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011339	hereditary spastic paraplegia 8	skos:exactMatch	DOID:0110823	hereditary spastic paraplegia 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0011342	SLC35A1-congenital disorder of glycosylation	skos:exactMatch	DOID:0070258	congenital disorder of glycosylation type IIf	semapv:ManualMappingCuration	2023-03-17
MONDO:0011346	xanthinuria type II	skos:exactMatch	DOID:0070453	xanthinuria type II	semapv:ManualMappingCuration	2024-04-21
MONDO:0011350	autosomal dominant nonsyndromic hearing loss 17	skos:exactMatch	DOID:0110548	autosomal dominant nonsyndromic deafness 17	semapv:ManualMappingCuration	2024-04-21
MONDO:0011359	acromelic frontonasal dysostosis	skos:exactMatch	DOID:0060342	acromelic frontonasal dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0011362	myopathy, myofibrillar, 9, with early respiratory failure	skos:exactMatch	DOID:0111188	myofibrillar myopathy 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0011365	blepharophimosis - intellectual disability syndrome, SBBYS type	skos:exactMatch	DOID:0060290	Ohdo syndrome, SBBYS variant	semapv:ManualMappingCuration	2023-03-17
MONDO:0011377	long QT syndrome 3	skos:exactMatch	DOID:0110646	long QT syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011381	dominant beta-thalassemia	skos:exactMatch	DOID:0080770	autosomal dominant beta thalassemia	semapv:ManualMappingCuration	2023-04-17
MONDO:0011382	sickle cell anemia	skos:exactMatch	DOID:0081445	sickle cell disease	semapv:ManualMappingCuration	2024-05-19
MONDO:0011382	sickle cell anemia	skos:exactMatch	DOID:10923	sickle cell anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011383	autoimmune lymphoproliferative syndrome type 2A	skos:exactMatch	DOID:0110115	autoimmune lymphoproliferative syndrome type 2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011391	megalencephalic leukoencephalopathy with subcortical cysts	skos:exactMatch	DOID:0080315	megalencephalic leukoencephalopathy with subcortical cysts	semapv:ManualMappingCuration	2023-03-17
MONDO:0011393	hypoalphalipoproteinemia, primary, 1	skos:exactMatch	DOID:0080957	primary hypoalphalipoproteinemia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0011395	cone-rod dystrophy 3	skos:exactMatch	DOID:0111013	cone-rod dystrophy 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0011397	autosomal dominant cerebellar ataxia, deafness and narcolepsy	skos:exactMatch	DOID:0050968	autosomal dominant cerebellar ataxia, deafness and narcolepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011399	alpha thalassemia spectrum	skos:exactMatch	DOID:1099	alpha thalassemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011400	dilated cardiomyopathy 1G	skos:exactMatch	DOID:0110430	dilated cardiomyopathy 1G	semapv:ManualMappingCuration	2024-02-18
MONDO:0011405	poikiloderma with neutropenia	skos:exactMatch	DOID:0060551	poikiloderma with neutropenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011408	hereditary spastic paraplegia 10	skos:exactMatch	DOID:0110763	hereditary spastic paraplegia 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0011412	familial encephalopathy with neuroserpin inclusion bodies	skos:exactMatch	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies	semapv:ManualMappingCuration	2023-03-17
MONDO:0011414	Peters anomaly	skos:exactMatch	DOID:0060673	Peters anomaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0011414	Peters anomaly	skos:exactMatch	DOID:0080610	anterior segment dysgenesis 5	semapv:ManualMappingCuration	2023-06-18
MONDO:0011417	hemochromatosis type 3	skos:exactMatch	DOID:0111030	hemochromatosis type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011421	mitochondrial complex V (ATP synthase) deficiency, nuclear type 1	skos:exactMatch	DOID:0050768	mitochondrial complex V (ATP synthase) deficiency nuclear type 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0011423	autosomal recessive limb-girdle muscular dystrophy type 2E	skos:exactMatch	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E	semapv:ManualMappingCuration	2023-03-17
MONDO:0011426	aceruloplasminemia	skos:exactMatch	DOID:0050711	aceruloplasminemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011428	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3	skos:exactMatch	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011436	autosomal recessive distal spinal muscular atrophy 1	skos:exactMatch	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011439	spinocerebellar ataxia type 12	skos:exactMatch	DOID:0050962	spinocerebellar ataxia type 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0011445	hereditary spastic paraplegia 11	skos:exactMatch	DOID:0110764	hereditary spastic paraplegia 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0011448	PPARG-related familial partial lipodystrophy	skos:exactMatch	DOID:0070204	familial partial lipodystrophy type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011451	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1	skos:exactMatch	DOID:0080357	mitochondrial complex IV deficiency nuclear type 2	semapv:ManualMappingCuration	2023-11-19
MONDO:0011456	nephronophthisis 3	skos:exactMatch	DOID:0111114	nephronophthisis 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0011459	arrhythmogenic right ventricular dysplasia 5	skos:exactMatch	DOID:0110074	arrhythmogenic right ventricular dysplasia 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0011461	generalized epilepsy with febrile seizures plus, type 2	skos:exactMatch	DOID:0111294	generalized epilepsy with febrile seizures plus 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0011462	pyogenic arthritis-pyoderma gangrenosum-acne syndrome	skos:exactMatch	DOID:0080519	PAPA syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011464	spinocerebellar ataxia type 11	skos:exactMatch	DOID:0050961	spinocerebellar ataxia type 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0011475	Charcot-Marie-Tooth disease type 4B2	skos:exactMatch	DOID:0110190	Charcot-Marie-Tooth disease type 4B2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011476	MHC class I deficiency	skos:exactMatch	DOID:0060009	MHC class I deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0011482	dilated cardiomyopathy 1I	skos:exactMatch	DOID:0110431	dilated cardiomyopathy 1I	semapv:ManualMappingCuration	2024-02-18
MONDO:0011484	catecholaminergic polymorphic ventricular tachycardia 1	skos:exactMatch	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011484	catecholaminergic polymorphic ventricular tachycardia 1	skos:exactMatch	DOID:0110071	arrhythmogenic right ventricular dysplasia 2	semapv:ManualMappingCuration	2023-07-09
MONDO:0011486	congenital muscular dystrophy 1B	skos:exactMatch	DOID:0110634	congenital muscular dystrophy 1B	semapv:ManualMappingCuration	2023-03-17
MONDO:0011489	hereditary spastic paraplegia 12	skos:exactMatch	DOID:0110765	hereditary spastic paraplegia 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0011493	Stickler syndrome type 2	skos:exactMatch	DOID:0080675	Stickler syndrome 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0011505	familial hypobetalipoproteinemia 2	skos:exactMatch	DOID:0111061	familial hypobetalipoproteinemia 2	semapv:ManualMappingCuration	2023-11-19
MONDO:0011512	Brooke-Spiegler syndrome	skos:exactMatch	DOID:0050693	Brooke-Spiegler syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011514	tricuspid atresia	skos:exactMatch	DOID:0080169	tricuspid atresia	semapv:ManualMappingCuration	2023-11-19
MONDO:0011522	hereditary spastic paraplegia 14	skos:exactMatch	DOID:0110767	hereditary spastic paraplegia 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0011527	Charcot-Marie-Tooth disease type 4E	skos:exactMatch	DOID:0110195	Charcot-Marie-Tooth disease type 4E	semapv:ManualMappingCuration	2023-03-17
MONDO:0011528	hyper-IgM syndrome type 2	skos:exactMatch	DOID:0060758	immunodeficiency with hyper-IgM type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011529	spinocerebellar ataxia type 13	skos:exactMatch	DOID:0050963	spinocerebellar ataxia type 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0011532	hereditary spastic paraplegia 13	skos:exactMatch	DOID:0110766	hereditary spastic paraplegia 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0011533	temtamy preaxial brachydactyly syndrome	skos:exactMatch	DOID:0050814	temtamy preaxial brachydactyly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011534	Charcot-Marie-Tooth disease type 4G	skos:exactMatch	DOID:0110196	Charcot-Marie-Tooth disease type 4G	semapv:ManualMappingCuration	2023-03-17
MONDO:0011535	split hand-foot malformation 4	skos:exactMatch	DOID:0090023	split hand-foot malformation 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0011537	macrocephaly-autism syndrome	skos:exactMatch	DOID:0060867	macrocephaly-autism syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011539	nemaline myopathy 5	skos:exactMatch	DOID:0110936	nemaline myopathy 5A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011540	spinocerebellar ataxia type 14	skos:exactMatch	DOID:0050964	spinocerebellar ataxia type 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0011541	dilated cardiomyopathy 1J	skos:exactMatch	DOID:0110440	dilated cardiomyopathy 1J	semapv:ManualMappingCuration	2023-03-17
MONDO:0011559	benign recurrent intrahepatic cholestasis type 2	skos:exactMatch	DOID:0070232	benign recurrent intrahepatic cholestasis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011565	metabolic syndrome X	skos:exactMatch	DOID:14221	abdominal obesity-metabolic syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011569	Charcot-Marie-Tooth disease type 2B1	skos:exactMatch	DOID:0110156	Charcot-Marie-Tooth disease type 2B1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011570	Charcot-Marie-Tooth disease type 2B2	skos:exactMatch	DOID:0110179	Charcot-Marie-Tooth disease type 2B2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011577	myopathy, proximal, and ophthalmoplegia	skos:exactMatch	DOID:0080719	congenital myopathy 6	semapv:ManualMappingCuration	2023-04-17
MONDO:0011579	late-onset retinal degeneration	skos:exactMatch	DOID:0060869	late-onset retinal degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0011581	arrhythmogenic cardiomyopathy with wooly hair and keratoderma	skos:exactMatch	DOID:0090128	Carvajal syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011582	multiple mitochondrial dysfunctions syndrome 1	skos:exactMatch	DOID:0080133	multiple mitochondrial dysfunctions syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011583	cerebral amyloid angiopathy, APP-related	skos:exactMatch	DOID:0070028	APP-related cerebral amyloid angiopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011584	Fanconi anemia complementation group D1	skos:exactMatch	DOID:0111089	Fanconi anemia complementation group D1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011585	autosomal recessive distal spinal muscular atrophy 2	skos:exactMatch	DOID:0111065	autosomal recessive distal hereditary motor neuronopathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011595	nonsyndromic congenital nail disorder 7	skos:exactMatch	DOID:0080085	nonsyndromic congenital nail disorder 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0011596	dermatitis, atopic, 2	skos:exactMatch	DOID:0110098	atopic dermatitis 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0011599	birdshot chorioretinopathy	skos:exactMatch	DOID:0111079	birdshot chorioretinopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011601	neonatal intrahepatic cholestasis due to citrin deficiency	skos:exactMatch	DOID:0070341	neonatal-onset type II citrullinemia	semapv:ManualMappingCuration	2023-06-18
MONDO:0011603	GNE myopathy	skos:exactMatch	DOID:0080718	GNE myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011610	dimethylglycine dehydrogenase deficiency	skos:exactMatch	DOID:0081446	dimethylglycine dehydrogenase deficiency	semapv:ManualMappingCuration	2024-05-19
MONDO:0011612	glycine encephalopathy	skos:exactMatch	DOID:9268	glycine encephalopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011614	3-hydroxy-3-methylglutaryl-CoA synthase deficiency	skos:exactMatch	DOID:0081168	HMG-CoA synthase 2 deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0011628	propionic acidemia	skos:exactMatch	DOID:14701	propionic acidemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011629	MOGS-congenital disorder of glycosylation	skos:exactMatch	DOID:0070254	congenital disorder of glycosylation type IIb	semapv:ManualMappingCuration	2023-03-17
MONDO:0011631	hemochromatosis type 4	skos:exactMatch	DOID:0111028	hemochromatosis type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0011633	Charcot-Marie-Tooth disease axonal type 2C	skos:exactMatch	DOID:0110182	Charcot-Marie-Tooth disease axonal type 2C	semapv:ManualMappingCuration	2023-03-17
MONDO:0011638	neuroferritinopathy	skos:exactMatch	DOID:0110737	neurodegeneration with brain iron accumulation 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011652	Phelan-McDermid syndrome	skos:exactMatch	DOID:0080354	Phelan-McDermid syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011661	inflammatory bowel disease 5	skos:exactMatch	DOID:0110889	inflammatory bowel disease 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0011664	immunodeficiency due to CD25 deficiency	skos:exactMatch	DOID:0111968	immunodeficiency 41	semapv:ManualMappingCuration	2023-04-17
MONDO:0011667	maturity-onset diabetes of the young type 4	skos:exactMatch	DOID:0111103	maturity-onset diabetes of the young type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0011668	maturity-onset diabetes of the young type 6	skos:exactMatch	DOID:0111104	maturity-onset diabetes of the young type 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0011669	hypotonia-cystinuria syndrome	skos:exactMatch	DOID:0060858	hypotonia-cystinuria syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011670	Ehlers-Danlos syndrome due to tenascin-X deficiency	skos:exactMatch	DOID:0080731	Ehlers-Danlos syndrome classic-like 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0011671	Huntington disease-like 2	skos:exactMatch	DOID:0090104	Huntington's disease-like 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011674	Charcot-Marie-Tooth disease dominant intermediate B	skos:exactMatch	DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B	semapv:ManualMappingCuration	2023-03-17
MONDO:0011675	Charcot-Marie-Tooth Disease, axonal, type 2GG	skos:exactMatch	DOID:0110202	Charcot-Marie-Tooth disease dominant intermediate A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011681	episodic ataxia type 4	skos:exactMatch	DOID:0050992	episodic ataxia type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0011682	episodic ataxia type 3	skos:exactMatch	DOID:0050991	episodic ataxia type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011683	oculocutaneous albinism type 4	skos:exactMatch	DOID:0070098	oculocutaneous albinism type IV	semapv:ManualMappingCuration	2023-03-17
MONDO:0011686	DNA ligase IV deficiency	skos:exactMatch	DOID:0060021	DNA ligase IV deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0011687	Charcot-Marie-Tooth disease axonal type 2F	skos:exactMatch	DOID:0110163	Charcot-Marie-Tooth disease axonal type 2F	semapv:ManualMappingCuration	2023-03-17
MONDO:0011688	muscular dystrophy-dystroglycanopathy type B5	skos:exactMatch	DOID:0110635	muscular dystrophy-dystroglycanopathy type B5	semapv:ManualMappingCuration	2023-03-17
MONDO:0011694	spinocerebellar ataxia type 15/16	skos:exactMatch	DOID:0050965	spinocerebellar ataxia type 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0011698	glycine N-methyltransferase deficiency	skos:exactMatch	DOID:0111037	glycine N-methyltransferase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0011702	dilated cardiomyopathy 1L	skos:exactMatch	DOID:0110436	dilated cardiomyopathy 1L	semapv:ManualMappingCuration	2024-02-18
MONDO:0011706	Kufor-Rakeb syndrome	skos:exactMatch	DOID:0060556	Kufor-Rakeb syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011708	autosomal dominant nonsyndromic hearing loss 36	skos:exactMatch	DOID:0110563	autosomal dominant nonsyndromic deafness 36	semapv:ManualMappingCuration	2024-04-21
MONDO:0011715	Seckel syndrome 2	skos:exactMatch	DOID:0070013	Seckel syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0011717	hyperinsulinism-hyperammonemia syndrome	skos:exactMatch	DOID:0070217	familial hyperinsulinemic hypoglycemia 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0011719	gastrointestinal stromal tumor	skos:exactMatch	DOID:9253	gastrointestinal stromal tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0011720	spermatogenic failure 3	skos:exactMatch	DOID:0070168	spermatogenic failure 3	semapv:ManualMappingCuration	2024-02-18
MONDO:0011721	distal myopathy with anterior tibial onset	skos:exactMatch	DOID:0111187	distal myopathy with anterior tibial onset	semapv:ManualMappingCuration	2023-03-17
MONDO:0011728	benign essential blepharospasm	skos:exactMatch	DOID:529	blepharospasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0011730	fumaric aciduria	skos:exactMatch	DOID:0111261	fumarase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0011735	hyper-IgM syndrome type 3	skos:exactMatch	DOID:0060023	immunodeficiency with hyper IgM type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011738	bilateral frontoparietal polymicrogyria	skos:exactMatch	DOID:0080922	bilateral frontoparietal polymicrogyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0011740	Carney-Stratakis syndrome	skos:exactMatch	DOID:0080533	Carney-Stratakis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011749	oculocutaneous albinism type 1B	skos:exactMatch	DOID:0070095	oculocutaneous albinism type IB	semapv:ManualMappingCuration	2023-03-17
MONDO:0011758	Hurler syndrome	skos:exactMatch	DOID:0111390	mucopolysaccharidosis Ih	semapv:ManualMappingCuration	2023-03-17
MONDO:0011759	Hurler-Scheie syndrome	skos:exactMatch	DOID:0111389	mucopolysaccharidosis Ih/s	semapv:ManualMappingCuration	2023-03-17
MONDO:0011760	Scheie syndrome	skos:exactMatch	DOID:0060222	Scheie syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011765	multiple epiphyseal dysplasia type 5	skos:exactMatch	DOID:0070299	multiple epiphyseal dysplasia 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0011767	autosomal recessive nonsyndromic hearing loss 31	skos:exactMatch	DOID:0110490	autosomal recessive nonsyndromic deafness 31	semapv:ManualMappingCuration	2024-04-21
MONDO:0011771	neuronopathy, distal hereditary motor, autosomal recessive 3	skos:exactMatch	DOID:0111211	autosomal recessive distal hereditary motor neuronopathy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011772	B4GALT1-congenital disorder of glycosylation	skos:exactMatch	DOID:0070256	congenital disorder of glycosylation type IId	semapv:ManualMappingCuration	2023-03-17
MONDO:0011773	anauxetic dysplasia	skos:exactMatch	DOID:0080942	anauxetic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011776	CINCA syndrome	skos:exactMatch	DOID:0090029	CINCA syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011781	spinocerebellar ataxia type 17	skos:exactMatch	DOID:0050967	spinocerebellar ataxia type 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0011783	ALG12-congenital disorder of glycosylation	skos:exactMatch	DOID:0080559	congenital disorder of glycosylation Ig	semapv:ManualMappingCuration	2023-03-17
MONDO:0011785	hereditary spastic paraplegia 19	skos:exactMatch	DOID:0110772	hereditary spastic paraplegia 19	semapv:ManualMappingCuration	2023-03-17
MONDO:0011787	autosomal recessive limb-girdle muscular dystrophy type 2I	skos:exactMatch	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I	semapv:ManualMappingCuration	2023-03-17
MONDO:0011789	familial meningioma	skos:exactMatch	DOID:4586	familial meningioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0011801	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1	skos:exactMatch	DOID:0090115	spinocerebellar ataxia with axonal neuropathy 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011803	hereditary spastic paraplegia 7	skos:exactMatch	DOID:0110816	hereditary spastic paraplegia 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0011804	autoimmune lymphoproliferative syndrome type 2B	skos:exactMatch	DOID:0110116	autoimmune lymphoproliferative syndrome type 2B	semapv:ManualMappingCuration	2023-03-17
MONDO:0011811	autosomal recessive cerebellar ataxia-saccadic intrusion syndrome	skos:exactMatch	DOID:0111611	autosomal recessive spinocerebellar ataxia 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0011812	Duane-radial ray syndrome	skos:exactMatch	DOID:0060747	Duane-radial ray syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011814	Smith-McCort dysplasia 1	skos:exactMatch	DOID:0081270	Smith-McCort dysplasia 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0011819	spinocerebellar ataxia type 19/22	skos:exactMatch	DOID:0050970	spinocerebellar ataxia type 19/22	semapv:ManualMappingCuration	2023-03-17
MONDO:0011821	Meckel syndrome, type 3	skos:exactMatch	DOID:0070117	Meckel syndrome 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0011822	Bartter disease type 3	skos:exactMatch	DOID:0110144	Bartter disease type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011829	coenzyme Q10 deficiency, primary, 1	skos:exactMatch	DOID:0070238	primary coenzyme Q10 deficiency 1	semapv:ManualMappingCuration	2024-02-18
MONDO:0011830	lissencephaly due to LIS1 mutation	skos:exactMatch	DOID:0112237	lissencephaly 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0011831	arrhythmogenic right ventricular dysplasia 8	skos:exactMatch	DOID:0110076	arrhythmogenic right ventricular dysplasia 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0011833	spinocerebellar ataxia type 21	skos:exactMatch	DOID:0050972	spinocerebellar ataxia type 21	semapv:ManualMappingCuration	2023-03-17
MONDO:0011834	spinocerebellar ataxia type 18	skos:exactMatch	DOID:0050969	spinocerebellar ataxia type 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0011835	sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	skos:exactMatch	DOID:0111276	sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0011837	vitamin K-dependent clotting factors, combined deficiency of, type 2	skos:exactMatch	DOID:0112174	combined deficiency of vitamin K-dependent clotting factors 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0011838	Bothnia retinal dystrophy	skos:exactMatch	DOID:0050683	Bothnia retinal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0011839	Newfoundland cone-rod dystrophy	skos:exactMatch	DOID:0111015	Newfoundland cone-rod dystrophy	semapv:ManualMappingCuration	2023-11-19
MONDO:0011840	dilated cardiomyopathy 1M	skos:exactMatch	DOID:0110449	dilated cardiomyopathy 1M	semapv:ManualMappingCuration	2024-02-18
MONDO:0011841	biotin-responsive basal ganglia disease	skos:exactMatch	DOID:0050659	biotin-responsive basal ganglia disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0011842	GRN-related frontotemporal lobar degeneration with Tdp43 inclusions	skos:exactMatch	DOID:0060672	GRN-related frontotemporal lobar degeneration with TDP43 inclusions	semapv:ManualMappingCuration	2023-03-17
MONDO:0011843	hypertrophic cardiomyopathy 25	skos:exactMatch	DOID:0110328	hypertrophic cardiomyopathy 25	semapv:ManualMappingCuration	2024-04-21
MONDO:0011852	nonsyndromic congenital nail disorder 8	skos:exactMatch	DOID:0080086	nonsyndromic congenital nail disorder 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0011855	granular corneal dystrophy type II	skos:exactMatch	DOID:0060444	granular corneal dystrophy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011856	spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome	skos:exactMatch	DOID:0112305	spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism	semapv:ManualMappingCuration	2023-04-17
MONDO:0011862	hereditary spastic paraplegia 24	skos:exactMatch	DOID:0110775	hereditary spastic paraplegia 24	semapv:ManualMappingCuration	2023-03-17
MONDO:0011868	lethal congenital contracture syndrome 2	skos:exactMatch	DOID:0060560	lethal congenital contracture syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011871	Niemann-Pick disease type B	skos:exactMatch	DOID:0070112	Niemann-Pick disease type B	semapv:ManualMappingCuration	2023-03-17
MONDO:0011872	Griscelli syndrome type 2	skos:exactMatch	DOID:0060833	Griscelli syndrome type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011875	epilepsy, idiopathic generalized, susceptibility to, 11	skos:exactMatch	DOID:0111312	idiopathic generalized epilepsy 11	semapv:ManualMappingCuration	2024-04-21
MONDO:0011877	autosomal dominant osteopetrosis 1	skos:exactMatch	DOID:0110937	autosomal dominant osteopetrosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011879	neuronopathy, distal hereditary motor, type 7B	skos:exactMatch	DOID:0111202	autosomal dominant distal hereditary motor neuronopathy 14	semapv:ManualMappingCuration	2024-04-21
MONDO:0011881	keratosis palmoplantaris striata 3	skos:exactMatch	DOID:0081110	keratosis palmoplantaris striata 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0011886	torsion dystonia 13	skos:exactMatch	DOID:0090037	torsion dystonia 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0011889	Charcot-Marie-Tooth disease type 2I	skos:exactMatch	DOID:0110158	Charcot-Marie-Tooth disease type 2I	semapv:ManualMappingCuration	2023-03-17
MONDO:0011890	Charcot-Marie-Tooth disease type 1D	skos:exactMatch	DOID:0110150	Charcot-Marie-Tooth disease type 1D	semapv:ManualMappingCuration	2023-03-17
MONDO:0011892	epilepsy, idiopathic generalized, susceptibility to, 9	skos:exactMatch	DOID:0111323	idiopathic generalized epilepsy 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0011894	Charcot-Marie-Tooth disease type 2E	skos:exactMatch	DOID:0110165	Charcot-Marie-Tooth disease type 2E	semapv:ManualMappingCuration	2023-03-17
MONDO:0011897	leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome	skos:exactMatch	DOID:0060794	hypomyelinating leukodystrophy 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0011899	Noonan syndrome-like disorder with loose anagen hair	skos:exactMatch	DOID:0080691	Noonan syndrome-like disorder with loose anagen hair	semapv:ManualMappingCuration	2023-03-17
MONDO:0011901	Charcot-Marie-Tooth disease axonal type 2H	skos:exactMatch	DOID:0110166	Charcot-Marie-Tooth disease axonal type 2H	semapv:ManualMappingCuration	2023-03-17
MONDO:0011902	Charcot-Marie-Tooth disease type 1F	skos:exactMatch	DOID:0110149	Charcot-Marie-Tooth disease type 1F	semapv:ManualMappingCuration	2023-03-17
MONDO:0011903	Charcot-Marie-Tooth disease type 2J	skos:exactMatch	DOID:0110157	Charcot-Marie-Tooth disease type 2J	semapv:ManualMappingCuration	2023-03-17
MONDO:0011906	congenital bile acid synthesis defect 1	skos:exactMatch	DOID:0111071	congenital bile acid synthesis defect 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0011907	acrocapitofemoral dysplasia	skos:exactMatch	DOID:0050604	acrocapitofemoral dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011909	Charcot-Marie-Tooth disease dominant intermediate D	skos:exactMatch	DOID:0110200	Charcot-Marie-Tooth disease dominant intermediate D	semapv:ManualMappingCuration	2023-03-17
MONDO:0011911	craniolenticulosutural dysplasia	skos:exactMatch	DOID:0070307	craniolenticulosutural dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0011913	Alzheimer disease 3	skos:exactMatch	DOID:0110042	Alzheimer's disease 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0011916	Charcot-Marie-Tooth disease axonal type 2K	skos:exactMatch	DOID:0110167	Charcot-Marie-Tooth disease axonal type 2K	semapv:ManualMappingCuration	2023-03-17
MONDO:0011925	congenital merosin-deficient muscular dystrophy 1A	skos:exactMatch	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A	semapv:ManualMappingCuration	2023-03-17
MONDO:0011929	chromosome 1p36 deletion syndrome	skos:exactMatch	DOID:0060410	chromosome 1p36 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011933	ALG2-congenital disorder of glycosylation	skos:exactMatch	DOID:0080561	congenital disorder of glycosylation Ii	semapv:ManualMappingCuration	2023-03-17
MONDO:0011934	dermatofibrosarcoma protuberans	skos:exactMatch	DOID:3507	dermatofibrosarcoma protuberans	semapv:ManualMappingCuration	2023-03-17
MONDO:0011936	microphthalmia with brain and digit anomalies	skos:exactMatch	DOID:0111805	syndromic microphthalmia 6	semapv:ManualMappingCuration	2023-04-17
MONDO:0011938	atrial septal defect 2	skos:exactMatch	DOID:0110107	atrial heart septal defect 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0011945	Gaucher disease perinatal lethal	skos:exactMatch	DOID:0110960	Gaucher's disease perinatal lethal	semapv:ManualMappingCuration	2023-03-17
MONDO:0011948	pontocerebellar hypoplasia type 3	skos:exactMatch	DOID:0060272	pontocerebellar hypoplasia type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0011950	infantile-onset autosomal recessive nonprogressive cerebellar ataxia	skos:exactMatch	DOID:0111617	autosomal recessive spinocerebellar ataxia 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0011957	retinal macular dystrophy type 2	skos:exactMatch	DOID:0070517	retinal macular dystrophy 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0011959	sweet syndrome	skos:exactMatch	DOID:0080746	Sweet syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011961	hereditary sensory and autonomic neuropathy type 1B	skos:exactMatch	DOID:0070148	hereditary sensory neuropathy type 1B	semapv:ManualMappingCuration	2023-03-17
MONDO:0011962	endometrial cancer	skos:exactMatch	DOID:1380	endometrial cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0011964	DPAGT1-congenital disorder of glycosylation	skos:exactMatch	DOID:0080562	congenital disorder of glycosylation Ij	semapv:ManualMappingCuration	2023-03-17
MONDO:0011965	familial temporal lobe epilepsy 2	skos:exactMatch	DOID:0060755	familial temporal lobe epilepsy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0011968	autosomal recessive limb-girdle muscular dystrophy type 2D	skos:exactMatch	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D	semapv:ManualMappingCuration	2023-03-17
MONDO:0011969	ALG8-congenital disorder of glycosylation	skos:exactMatch	DOID:0080560	congenital disorder of glycosylation Ih	semapv:ManualMappingCuration	2023-03-17
MONDO:0011970	rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome	skos:exactMatch	DOID:0111645	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011971	hyper-IgM syndrome type 5	skos:exactMatch	DOID:0060759	immunodeficiency with hyper IgM type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0011972	ovarian hyperstimulation syndrome	skos:exactMatch	DOID:5425	ovarian hyperstimulation syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0011985	hyper-IgM syndrome type 4	skos:exactMatch	DOID:0060760	immunodeficiency with hyper-IgM type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0011988	neutrophil immunodeficiency syndrome	skos:exactMatch	DOID:0112064	immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis	semapv:ManualMappingCuration	2023-04-17
MONDO:0011992	hereditary spastic paraplegia 25	skos:exactMatch	DOID:0110776	hereditary spastic paraplegia 25	semapv:ManualMappingCuration	2023-03-17
MONDO:0011997	Hermansky-Pudlak syndrome 2	skos:exactMatch	DOID:0060540	Hermansky-Pudlak syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012012	Charcot-Marie-Tooth disease dominant intermediate C	skos:exactMatch	DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C	semapv:ManualMappingCuration	2023-03-17
MONDO:0012014	Charcot-Marie-Tooth disease recessive intermediate A	skos:exactMatch	DOID:0110201	Charcot-Marie-Tooth disease recessive intermediate A	semapv:ManualMappingCuration	2023-03-17
MONDO:0012019	spondyloepiphyseal dysplasia, Kimberley type	skos:exactMatch	DOID:0112282	spondyloepiphyseal dysplasia Kimberley type	semapv:ManualMappingCuration	2023-06-18
MONDO:0012020	chromosome 22q11.2 microduplication syndrome	skos:exactMatch	DOID:0060436	chromosome 22q11.2 microduplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012031	platelet-type bleeding disorder 10	skos:exactMatch	DOID:0111046	platelet-type bleeding disorder 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0012033	bradyopsia	skos:exactMatch	DOID:0050335	bradyopsia	semapv:ManualMappingCuration	2023-03-17
MONDO:0012034	autosomal dominant limb-girdle muscular dystrophy type 1F	skos:exactMatch	DOID:0110304	autosomal dominant limb-girdle muscular dystrophy type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012041	familial adenomatous polyposis 2	skos:exactMatch	DOID:0080410	familial adenomatous polyposis 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012043	Reis-Bucklers corneal dystrophy	skos:exactMatch	DOID:0060453	Reis-Bucklers corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0012052	ALG1-congenital disorder of glycosylation	skos:exactMatch	DOID:0080563	congenital disorder of glycosylation Ik	semapv:ManualMappingCuration	2023-03-17
MONDO:0012056	Leber congenital amaurosis 9	skos:exactMatch	DOID:0110005	Leber congenital amaurosis 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0012062	dilated cardiomyopathy 1O	skos:exactMatch	DOID:0110451	dilated cardiomyopathy 1O	semapv:ManualMappingCuration	2024-02-18
MONDO:0012064	choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome	skos:exactMatch	DOID:0080695	Burn-McKeown syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0012072	familial partial lipodystrophy, Kobberling type	skos:exactMatch	DOID:0070207	familial partial lipodystrophy type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0012074	mandibuloacral dysplasia with type B lipodystrophy	skos:exactMatch	DOID:0081129	mandibuloacral dysplasia type B lipodystrophy	semapv:ManualMappingCuration	2023-06-18
MONDO:0012077	amyotrophic lateral sclerosis type 8	skos:exactMatch	DOID:0050752	amyotrophic lateral sclerosis type 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0012080	neuronopathy, distal hereditary motor, type 2B	skos:exactMatch	DOID:0111207	autosomal dominant distal hereditary motor neuronopathy 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0012083	autosomal dominant nonsyndromic hearing loss 28	skos:exactMatch	DOID:0110557	autosomal dominant nonsyndromic deafness 28	semapv:ManualMappingCuration	2024-04-21
MONDO:0012084	aromatic L-amino acid decarboxylase deficiency	skos:exactMatch	DOID:0090123	aromatic L-amino acid decarboxylase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012088	primary ciliary dyskinesia 5	skos:exactMatch	DOID:0110617	primary ciliary dyskinesia 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012092	hereditary sensory and autonomic neuropathy type 5	skos:exactMatch	DOID:0070145	hereditary sensory and autonomic neuropathy type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012096	Charcot-Marie-Tooth disease axonal type 2L	skos:exactMatch	DOID:0110174	Charcot-Marie-Tooth disease axonal type 2L	semapv:ManualMappingCuration	2023-03-17
MONDO:0012098	spinocerebellar ataxia type 20	skos:exactMatch	DOID:0050971	spinocerebellar ataxia type 20	semapv:ManualMappingCuration	2023-03-17
MONDO:0012103	spinocerebellar ataxia type 25	skos:exactMatch	DOID:0050974	spinocerebellar ataxia type 25	semapv:ManualMappingCuration	2023-03-17
MONDO:0012112	hypertrophic cardiomyopathy 10	skos:exactMatch	DOID:0110316	hypertrophic cardiomyopathy 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0012116	spinocerebellar ataxia type 8	skos:exactMatch	DOID:0050959	spinocerebellar ataxia type 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0012117	ALG9-congenital disorder of glycosylation	skos:exactMatch	DOID:0080564	congenital disorder of glycosylation Il	semapv:ManualMappingCuration	2023-03-17
MONDO:0012118	COG7-congenital disorder of glycosylation	skos:exactMatch	DOID:0070257	congenital disorder of glycosylation type IIe	semapv:ManualMappingCuration	2024-04-21
MONDO:0012123	congenital disorder of glycosylation type 1E	skos:exactMatch	DOID:0080557	congenital disorder of glycosylation Ie	semapv:ManualMappingCuration	2023-03-17
MONDO:0012125	hypomyelinating leukodystrophy 2	skos:exactMatch	DOID:0060787	hypomyelinating leukodystrophy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012127	autosomal recessive limb-girdle muscular dystrophy type 2J	skos:exactMatch	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J	semapv:ManualMappingCuration	2023-03-17
MONDO:0012128	transposition of the great arteries, dextro-looped	skos:exactMatch	DOID:0060771	dextro-looped transposition of the great arteries 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0012130	myofibrillar myopathy 2	skos:exactMatch	DOID:0080093	myofibrillar myopathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012138	muscular dystrophy-dystroglycanopathy type B6	skos:exactMatch	DOID:0110637	muscular dystrophy-dystroglycanopathy type B6	semapv:ManualMappingCuration	2023-03-17
MONDO:0012141	orofacial cleft 6, susceptibility to	skos:exactMatch	DOID:0080593	orofacial cleft 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0012142	orofacial cleft 5	skos:exactMatch	DOID:0080399	orofacial cleft 5	semapv:ManualMappingCuration	2023-11-19
MONDO:0012155	choanal atresia	skos:exactMatch	DOID:9574	choanal atresia	semapv:ManualMappingCuration	2023-03-17
MONDO:0012160	spondylometaphyseal dysplasia-cone-rod dystrophy syndrome	skos:exactMatch	DOID:0112300	spondylometaphyseal dysplasia with cone-rod dystrophy	semapv:ManualMappingCuration	2023-04-17
MONDO:0012163	immunodeficiency 104	skos:exactMatch	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive	semapv:ManualMappingCuration	2023-03-17
MONDO:0012166	autosomal dominant sensory ataxia 1	skos:exactMatch	DOID:0111170	autosomal dominant sensory ataxia 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0012172	mitochondrial trifunctional protein deficiency	skos:exactMatch	DOID:0111277	mitochondrial trifunctional protein deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012181	hereditary spastic paraplegia 27	skos:exactMatch	DOID:0110778	hereditary spastic paraplegia 27	semapv:ManualMappingCuration	2023-03-17
MONDO:0012184	Pierson syndrome	skos:exactMatch	DOID:0060852	Pierson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012185	spondylometaphyseal dysplasia, A4 type	skos:exactMatch	DOID:0112301	spondylometaphyseal dysplasia type A4	semapv:ManualMappingCuration	2023-06-18
MONDO:0012186	Fanconi anemia complementation group I	skos:exactMatch	DOID:0111091	Fanconi anemia complementation group I	semapv:ManualMappingCuration	2023-03-17
MONDO:0012187	Fanconi anemia complementation group J	skos:exactMatch	DOID:0111097	Fanconi anemia complementation group J	semapv:ManualMappingCuration	2023-03-17
MONDO:0012188	neuronal ceroid lipofuscinosis 9	skos:exactMatch	DOID:0110733	neuronal ceroid lipofuscinosis 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0012191	hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	skos:exactMatch	DOID:0111474	combined oxidative phosphorylation deficiency 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0012193	autosomal dominant limb-girdle muscular dystrophy type 1G	skos:exactMatch	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012195	arthrogryposis-severe scoliosis syndrome	skos:exactMatch	DOID:0111610	distal arthrogryposis type 4	semapv:ManualMappingCuration	2023-04-17
MONDO:0012198	PCWH syndrome	skos:exactMatch	DOID:0090111	PCWH syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012203	familial hyperthyroidism due to mutations in TSH receptor	skos:exactMatch	DOID:0081101	nonautoimmune hyperthyroidism	semapv:ManualMappingCuration	2023-04-17
MONDO:0012211	MPDU1-congenital disorder of glycosylation	skos:exactMatch	DOID:0080558	congenital disorder of glycosylation If	semapv:ManualMappingCuration	2023-03-17
MONDO:0012212	Loeys-Dietz syndrome 1	skos:exactMatch	DOID:0070235	Loeys-Dietz syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0012213	hereditary spastic paraplegia 26	skos:exactMatch	DOID:0110777	hereditary spastic paraplegia 26	semapv:ManualMappingCuration	2023-03-17
MONDO:0012215	myofibrillar myopathy 3	skos:exactMatch	DOID:0080094	myofibrillar myopathy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012216	foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome	skos:exactMatch	DOID:0070531	foveal hypoplasia 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0012220	Griscelli syndrome type 3	skos:exactMatch	DOID:0060834	Griscelli syndrome type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012221	alpha-N-acetylgalactosaminidase deficiency type 1	skos:exactMatch	DOID:0112318	Schindler disease type 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0012222	alpha-N-acetylgalactosaminidase deficiency type 2	skos:exactMatch	DOID:0112319	Kanzaki disease	semapv:ManualMappingCuration	2023-04-17
MONDO:0012231	Charcot-Marie-Tooth disease type 2A2	skos:exactMatch	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0012235	autosomal recessive spinocerebellar ataxia 7	skos:exactMatch	DOID:0080059	autosomal recessive spinocerebellar ataxia 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0012237	nemaline myopathy 6	skos:exactMatch	DOID:0110935	nemaline myopathy 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0012238	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2	skos:exactMatch	DOID:0111517	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012239	congenital myopathy 4B, autosomal recessive	skos:exactMatch	DOID:0110926	nemaline myopathy 1	semapv:ManualMappingCuration	2023-09-24
MONDO:0012240	congenital myopathy 23	skos:exactMatch	DOID:0110932	nemaline myopathy 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0012241	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3	skos:exactMatch	DOID:0111520	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012246	spinocerebellar ataxia type 26	skos:exactMatch	DOID:0050975	spinocerebellar ataxia type 26	semapv:ManualMappingCuration	2023-03-17
MONDO:0012247	spinocerebellar ataxia type 27	skos:exactMatch	DOID:0050976	spinocerebellar ataxia type 27	semapv:ManualMappingCuration	2023-03-17
MONDO:0012248	autosomal recessive limb-girdle muscular dystrophy type 2K	skos:exactMatch	DOID:0110297	autosomal recessive limb-girdle muscular dystrophy type 2K	semapv:ManualMappingCuration	2023-03-17
MONDO:0012250	Charcot-Marie-Tooth disease type 4H	skos:exactMatch	DOID:0110192	Charcot-Marie-Tooth disease type 4H	semapv:ManualMappingCuration	2023-03-17
MONDO:0012251	MEDNIK syndrome	skos:exactMatch	DOID:0060483	MEDNIK syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012256	hereditary spastic paraplegia 28	skos:exactMatch	DOID:0110779	hereditary spastic paraplegia 28	semapv:ManualMappingCuration	2023-03-17
MONDO:0012269	chromosome 3q29 microdeletion syndrome	skos:exactMatch	DOID:0060419	chromosome 3q29 microdeletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012274	acromesomelic dysplasia 3	skos:exactMatch	DOID:0081237	acromesomelic dysplasia-3	semapv:ManualMappingCuration	2023-06-18
MONDO:0012276	generalized epilepsy-paroxysmal dyskinesia syndrome	skos:exactMatch	DOID:0070442	paroxysmal nonkinesigenic dyskinesia 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0012277	myofibrillar myopathy 4	skos:exactMatch	DOID:0080095	myofibrillar myopathy 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012280	Goldberg-Shprintzen syndrome	skos:exactMatch	DOID:0060481	Goldberg-Shprintzen syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012289	myofibrillar myopathy 5	skos:exactMatch	DOID:0080096	myofibrillar myopathy 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012290	CEDNIK syndrome	skos:exactMatch	DOID:0060337	CEDNIK syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012297	spastic paraplegia, optic atropy, and neuropathy	skos:exactMatch	DOID:0060491	SPOAN syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012301	mitochondrial DNA depletion syndrome, myopathic form	skos:exactMatch	DOID:0080120	mitochondrial DNA depletion syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012308	Joubert syndrome with renal defect	skos:exactMatch	DOID:0110999	Joubert syndrome 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012315	distal 10q deletion syndrome	skos:exactMatch	DOID:0060390	distal 10q deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012320	migraine, familial hemiplegic, 3	skos:exactMatch	DOID:0111183	familial hemiplegic migraine 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012322	holoprosencephaly 5	skos:exactMatch	DOID:0110878	holoprosencephaly 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012333	autosomal recessive nonsyndromic hearing loss 53	skos:exactMatch	DOID:0110509	autosomal recessive nonsyndromic deafness 53	semapv:ManualMappingCuration	2024-04-21
MONDO:0012334	hereditary spastic paraplegia 29	skos:exactMatch	DOID:0110780	hereditary spastic paraplegia 29	semapv:ManualMappingCuration	2023-03-17
MONDO:0012342	7q11.23 microduplication syndrome	skos:exactMatch	DOID:0080926	7q11.23 duplication syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0012345	acral peeling skin syndrome	skos:exactMatch	DOID:0070521	peeling skin syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0012351	zygodactyly type 1	skos:exactMatch	DOID:0111820	zygodactyly 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0012353	erythrocytosis, familial, 3	skos:exactMatch	DOID:0080338	familial erythrocytosis 3	semapv:ManualMappingCuration	2024-02-18
MONDO:0012354	platelet-type bleeding disorder 8	skos:exactMatch	DOID:0060692	platelet-type bleeding disorder 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0012363	retinitis pigmentosa 32	skos:exactMatch	DOID:0110355	retinitis pigmentosa 32	semapv:ManualMappingCuration	2023-03-17
MONDO:0012381	hyperinsulinism due to INSR deficiency	skos:exactMatch	DOID:0070220	familial hyperinsulinemic hypoglycemia 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012382	hyperinsulinemic hypoglycemia, familial, 4	skos:exactMatch	DOID:0070215	familial hyperinsulinemic hypoglycemia 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012383	primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency	skos:exactMatch	DOID:0111967	immunodeficiency 54	semapv:ManualMappingCuration	2023-04-17
MONDO:0012391	neuronal ceroid lipofuscinosis 8 northern epilepsy variant	skos:exactMatch	DOID:0110724	neuronal ceroid lipofuscinosis 8 northern epilepsy variant	semapv:ManualMappingCuration	2023-03-17
MONDO:0012393	congenital brain dysgenesis due to glutamine synthetase deficiency	skos:exactMatch	DOID:0070544	congenital glutamine deficiency	semapv:ManualMappingCuration	2024-07-21
MONDO:0012394	multiple synostoses syndrome 2	skos:exactMatch	DOID:0081318	multiple synostoses syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0012396	exercise-induced hyperinsulinism	skos:exactMatch	DOID:0070214	familial hyperinsulinemic hypoglycemia 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0012399	complex cortical dysplasia with other brain malformations 7	skos:exactMatch	DOID:0090132	complex cortical dysplasia with other brain malformations 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0012400	cortical dysplasia-focal epilepsy syndrome	skos:exactMatch	DOID:0090130	cortical dysplasia-focal epilepsy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012401	congenital stromal corneal dystrophy	skos:exactMatch	DOID:0060445	congenital stromal corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0012407	pyridoxal phosphate-responsive seizures	skos:exactMatch	DOID:0111329	pyridoxamine 5'-phosphate oxidase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012410	Finnish upper limb-onset distal myopathy	skos:exactMatch	DOID:0111189	distal myopathy 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0012411	giant axonal neuropathy 2	skos:exactMatch	DOID:0090069	giant axonal neuropathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012413	syndromic microphthalmia type 5	skos:exactMatch	DOID:0111806	syndromic microphthalmia 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0012414	neuronal ceroid lipofuscinosis 10	skos:exactMatch	DOID:0110725	neuronal ceroid lipofuscinosis 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0012415	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4	skos:exactMatch	DOID:0111525	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4	semapv:ManualMappingCuration	2023-11-19
MONDO:0012419	age related macular degeneration 7	skos:exactMatch	DOID:0110019	age related macular degeneration 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0012426	immunodeficiency 25	skos:exactMatch	DOID:0060007	CD3zeta deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012426	immunodeficiency 25	skos:exactMatch	DOID:0111942	immunodeficiency 25	semapv:ManualMappingCuration	2023-03-17
MONDO:0012432	Joubert syndrome 5	skos:exactMatch	DOID:0111000	Joubert syndrome 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0012434	arrhythmogenic right ventricular dysplasia 10	skos:exactMatch	DOID:0110081	arrhythmogenic right ventricular dysplasia 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0012435	3-methylglutaconic aciduria type 5	skos:exactMatch	DOID:0110000	3-methylglutaconic aciduria type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012436	neonatal diabetes mellitus with congenital hypothyroidism	skos:exactMatch	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism	semapv:ManualMappingCuration	2023-03-17
MONDO:0012438	pontocerebellar hypoplasia type 5	skos:exactMatch	DOID:0060274	pontocerebellar hypoplasia type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012448	hereditary spastic paraplegia 33	skos:exactMatch	DOID:0110784	hereditary spastic paraplegia 33	semapv:ManualMappingCuration	2023-09-24
MONDO:0012449	spinocerebellar ataxia type 23	skos:exactMatch	DOID:0050973	spinocerebellar ataxia type 23	semapv:ManualMappingCuration	2023-03-17
MONDO:0012450	spinocerebellar ataxia type 28	skos:exactMatch	DOID:0050977	spinocerebellar ataxia type 28	semapv:ManualMappingCuration	2023-03-17
MONDO:0012453	hereditary spastic paraplegia 31	skos:exactMatch	DOID:0110782	hereditary spastic paraplegia 31	semapv:ManualMappingCuration	2023-03-17
MONDO:0012455	Kleefstra syndrome	skos:exactMatch	DOID:0080597	Kleefstra syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012456	congenital primary aphakia	skos:exactMatch	DOID:0080607	anterior segment dysgenesis 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0012456	congenital primary aphakia	skos:exactMatch	DOID:11367	congenital aphakia	semapv:ManualMappingCuration	2023-03-17
MONDO:0012475	cone dystrophy with supernormal rod response	skos:exactMatch	DOID:0081022	retinal cone dystrophy 3B	semapv:ManualMappingCuration	2023-04-17
MONDO:0012476	hereditary spastic paraplegia 30	skos:exactMatch	DOID:0110781	hereditary spastic paraplegia 30	semapv:ManualMappingCuration	2023-03-17
MONDO:0012479	congenital malabsorptive diarrhea 4	skos:exactMatch	DOID:0060779	congenital malabsorptive diarrhea 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012481	mevalonic aciduria	skos:exactMatch	DOID:0050452	mevalonic aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0012495	spondyloepimetaphyseal dysplasia, Genevieve type	skos:exactMatch	DOID:0080576	spondyloepimetaphyseal dysplasia, Genevieve-type	semapv:ManualMappingCuration	2023-03-17
MONDO:0012502	normophosphatemic familial tumoral calcinosis	skos:exactMatch	DOID:0080170	normophosphatemic familial tumoral calcinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0012503	thiopurine S-methyltransferase deficiency	skos:exactMatch	DOID:0080172	thiopurine S-methyltransferase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012504	camptodactyly-tall stature-scoliosis-hearing loss syndrome	skos:exactMatch	DOID:0111160	camptodactyly-tall stature-scoliosis-hearing loss syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012510	combined oxidative phosphorylation defect type 2	skos:exactMatch	DOID:0111483	combined oxidative phosphorylation deficiency 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012511	preterm premature rupture of the membranes	skos:exactMatch	DOID:0111144	preterm premature rupture of the membranes	semapv:ManualMappingCuration	2023-03-17
MONDO:0012512	fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3	skos:exactMatch	DOID:0111486	combined oxidative phosphorylation deficiency 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012514	hypomyelinating leukodystrophy 5	skos:exactMatch	DOID:0060793	hypomyelinating leukodystrophy 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012516	mandibulofacial dysostosis-microcephaly syndrome	skos:exactMatch	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type	semapv:ManualMappingCuration	2023-03-17
MONDO:0012517	Gaucher disease due to saposin C deficiency	skos:exactMatch	DOID:0110961	atypical Gaucher's disease due to saposin C deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012526	hereditary angioedema type 3	skos:exactMatch	DOID:0080940	hereditary angioedema type III	semapv:ManualMappingCuration	2023-06-18
MONDO:0012531	xeroderma pigmentosum group B	skos:exactMatch	DOID:0110850	xeroderma pigmentosum group B	semapv:ManualMappingCuration	2023-03-17
MONDO:0012534	combined oxidative phosphorylation defect type 4	skos:exactMatch	DOID:0111494	combined oxidative phosphorylation deficiency 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012538	nemaline myopathy 7	skos:exactMatch	DOID:0110934	nemaline myopathy 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0012539	Joubert syndrome 6	skos:exactMatch	DOID:0111001	Joubert syndrome 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0012540	age related macular degeneration 4	skos:exactMatch	DOID:0110017	age related macular degeneration 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0012544	brachydactyly-syndactyly syndrome	skos:exactMatch	DOID:0050689	brachydactyly-syndactyly syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012548	Kostmann syndrome	skos:exactMatch	DOID:0112133	severe congenital neutropenia 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0012549	autosomal recessive ataxia, Beauce type	skos:exactMatch	DOID:0111618	autosomal recessive spinocerebellar ataxia 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0012552	multiple endocrine neoplasia type 4	skos:exactMatch	DOID:0080137	multiple endocrine neoplasia type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012553	cerebrooculofacioskeletal syndrome 2	skos:exactMatch	DOID:0080912	cerebrooculofacioskeletal syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0012556	DK1-congenital disorder of glycosylation	skos:exactMatch	DOID:0080565	congenital disorder of glycosylation Im	semapv:ManualMappingCuration	2023-03-17
MONDO:0012561	congenital anomalies of kidney and urinary tract 1	skos:exactMatch	DOID:0080206	CAKUT1	semapv:ManualMappingCuration	2023-03-17
MONDO:0012563	holoprosencephaly 9	skos:exactMatch	DOID:0110873	holoprosencephaly 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0012565	Fanconi anemia complementation group N	skos:exactMatch	DOID:0111094	Fanconi anemia complementation group N	semapv:ManualMappingCuration	2023-03-17
MONDO:0012574	Potocki-Lupski syndrome	skos:exactMatch	DOID:0060853	Potocki-Lupski syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012588	neuronal ceroid lipofuscinosis 7	skos:exactMatch	DOID:0110722	neuronal ceroid lipofuscinosis 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0012589	Pitt-Hopkins syndrome	skos:exactMatch	DOID:0060488	Pitt-Hopkins syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012590	XFE progeroid syndrome	skos:exactMatch	DOID:0060590	XFE progeroid syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012591	osteogenesis imperfecta type 5	skos:exactMatch	DOID:0110344	osteogenesis imperfecta type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012594	complement factor I deficiency	skos:exactMatch	DOID:0050419	complement factor I deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012596	PSAT deficiency	skos:exactMatch	DOID:0050723	PSAT deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012605	isolated microphthalmia 5	skos:exactMatch	DOID:0060837	isolated microphthalmia 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012608	neuronopathy, distal hereditary motor, autosomal recessive 4	skos:exactMatch	DOID:0111213	autosomal recessive distal hereditary motor neuronopathy 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012611	polyhydramnios, megalencephaly, and symptomatic epilepsy	skos:exactMatch	DOID:0070511	polyhydramnios, megalencephaly, and symptomatic epilepsy	semapv:ManualMappingCuration	2024-04-21
MONDO:0012624	acyl-CoA dehydrogenase 9 deficiency	skos:exactMatch	DOID:0112072	nuclear type mitochondrial complex I deficiency 20	semapv:ManualMappingCuration	2023-04-17
MONDO:0012625	retinitis pigmentosa 37	skos:exactMatch	DOID:0110399	retinitis pigmentosa 37	semapv:ManualMappingCuration	2024-04-21
MONDO:0012626	Meckel syndrome, type 4	skos:exactMatch	DOID:0070118	Meckel syndrome 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0012635	COG8-congenital disorder of glycosylation	skos:exactMatch	DOID:0070260	congenital disorder of glycosylation type IIh	semapv:ManualMappingCuration	2023-03-17
MONDO:0012637	COG1-congenital disorder of glycosylation	skos:exactMatch	DOID:0070259	congenital disorder of glycosylation type IIg	semapv:ManualMappingCuration	2023-03-17
MONDO:0012638	microphthalmia-brain atrophy syndrome	skos:exactMatch	DOID:0111812	syndromic microphthalmia 10	semapv:ManualMappingCuration	2023-04-17
MONDO:0012639	hereditary spastic paraplegia 18	skos:exactMatch	DOID:0110771	hereditary spastic paraplegia 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0012640	Charcot-Marie-Tooth disease type 4J	skos:exactMatch	DOID:0110184	Charcot-Marie-Tooth disease type 4J	semapv:ManualMappingCuration	2023-03-17
MONDO:0012643	hereditary spastic paraplegia 32	skos:exactMatch	DOID:0110783	hereditary spastic paraplegia 32	semapv:ManualMappingCuration	2023-03-17
MONDO:0012651	spastic ataxia 2	skos:exactMatch	DOID:0050941	spastic ataxia 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012652	autosomal recessive limb-girdle muscular dystrophy type 2L	skos:exactMatch	DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L	semapv:ManualMappingCuration	2023-03-17
MONDO:0012656	lethal congenital contracture syndrome 3	skos:exactMatch	DOID:0060653	lethal congenital contracture syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012658	brachydactyly type B2	skos:exactMatch	DOID:0110975	brachydactyly type B2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012659	age related macular degeneration 9	skos:exactMatch	DOID:0110021	age related macular degeneration 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0012662	Usher syndrome type 2D	skos:exactMatch	DOID:0110840	Usher syndrome type 2D	semapv:ManualMappingCuration	2023-03-17
MONDO:0012664	spastic ataxia 3	skos:exactMatch	DOID:0050942	spastic ataxia 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012665	cataract 33	skos:exactMatch	DOID:0110264	cataract 33	semapv:ManualMappingCuration	2023-03-17
MONDO:0012667	dilated cardiomyopathy 1W	skos:exactMatch	DOID:0110446	dilated cardiomyopathy 1W	semapv:ManualMappingCuration	2024-02-18
MONDO:0012669	Legius syndrome	skos:exactMatch	DOID:0070484	Legius syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0012670	autosomal recessive nonsyndromic hearing loss 63	skos:exactMatch	DOID:0110515	autosomal recessive nonsyndromic deafness 63	semapv:ManualMappingCuration	2023-03-17
MONDO:0012675	corticosteroid-binding globulin deficiency	skos:exactMatch	DOID:0090030	corticosteroid-binding globulin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012676	autosomal recessive osteopetrosis 4	skos:exactMatch	DOID:0110944	autosomal recessive osteopetrosis 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012679	autosomal recessive osteopetrosis 6	skos:exactMatch	DOID:0110945	autosomal recessive osteopetrosis 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0012682	immunodeficiency 35	skos:exactMatch	DOID:0111989	immunodeficiency 35	semapv:ManualMappingCuration	2023-03-17
MONDO:0012683	pontocerebellar hypoplasia type 6	skos:exactMatch	DOID:0060275	pontocerebellar hypoplasia type 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0012684	arrhythmogenic right ventricular dysplasia 12	skos:exactMatch	DOID:0110083	arrhythmogenic right ventricular dysplasia 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0012698	Waardenburg syndrome type 2E	skos:exactMatch	DOID:0110956	Waardenburg syndrome type 2E	semapv:ManualMappingCuration	2024-04-21
MONDO:0012699	autosomal recessive limb-girdle muscular dystrophy type 2M	skos:exactMatch	DOID:0110296	autosomal recessive limb-girdle muscular dystrophy type 2M	semapv:ManualMappingCuration	2023-03-17
MONDO:0012701	cataract 12 multiple types	skos:exactMatch	DOID:0110239	cataract 12 multiple types	semapv:ManualMappingCuration	2023-03-17
MONDO:0012704	dilated cardiomyopathy 1X	skos:exactMatch	DOID:0110444	dilated cardiomyopathy 1X	semapv:ManualMappingCuration	2024-02-18
MONDO:0012714	early-onset myopathy with fatal cardiomyopathy	skos:exactMatch	DOID:0081341	congenital myopathy 5	semapv:ManualMappingCuration	2023-07-09
MONDO:0012716	spondyloepiphyseal dysplasia, Cantu type	skos:exactMatch	DOID:0112287	spondyloepiphyseal dysplasia-brachydactyly and distinctive speech	semapv:ManualMappingCuration	2023-04-17
MONDO:0012718	hypotonia with lactic acidemia and hyperammonemia	skos:exactMatch	DOID:0111473	combined oxidative phosphorylation deficiency 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012719	combined PSAP deficiency	skos:exactMatch	DOID:0111330	combined saposin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012721	progressive myoclonic epilepsy type 3	skos:exactMatch	DOID:0111446	progressive myoclonus epilepsy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0012723	Leber congenital amaurosis 10	skos:exactMatch	DOID:0110291	Leber congenital amaurosis 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0012724	familial cold autoinflammatory syndrome 2	skos:exactMatch	DOID:0090063	familial cold autoinflammatory syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012729	erythrocytosis, familial, 4	skos:exactMatch	DOID:0080339	familial erythrocytosis 4	semapv:ManualMappingCuration	2024-02-18
MONDO:0012733	autosomal recessive bestrophinopathy	skos:exactMatch	DOID:0050662	bestrophinopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0012736	long QT syndrome 9	skos:exactMatch	DOID:0110650	long QT syndrome 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0012737	long QT syndrome 10	skos:exactMatch	DOID:0110651	long QT syndrome 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0012738	long QT syndrome 11	skos:exactMatch	DOID:0110652	long QT syndrome 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0012740	chromosome 22q11.2 deletion syndrome, distal	skos:exactMatch	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal	semapv:ManualMappingCuration	2023-03-17
MONDO:0012742	Brugada syndrome 3	skos:exactMatch	DOID:0110220	Brugada syndrome 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0012745	dilated cardiomyopathy 1Z	skos:exactMatch	DOID:0110434	dilated cardiomyopathy 1Z	semapv:ManualMappingCuration	2024-02-18
MONDO:0012746	dilated cardiomyopathy 2A	skos:exactMatch	DOID:0110460	dilated cardiomyopathy 2A	semapv:ManualMappingCuration	2024-02-18
MONDO:0012755	episodic ataxia type 7	skos:exactMatch	DOID:0050995	episodic ataxia type 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0012756	proximal 16p11.2 microdeletion syndrome	skos:exactMatch	DOID:0070515	chromosome 16p11.2 deletion syndrome, 593-kb	semapv:ManualMappingCuration	2024-04-21
MONDO:0012761	chromosome 3q29 microduplication syndrome	skos:exactMatch	DOID:0060459	chromosome 3q29 microduplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012766	hereditary spastic paraplegia 37	skos:exactMatch	DOID:0110788	hereditary spastic paraplegia 37	semapv:ManualMappingCuration	2023-03-17
MONDO:0012767	age related macular degeneration 11	skos:exactMatch	DOID:0110023	age related macular degeneration 11	semapv:ManualMappingCuration	2024-04-21
MONDO:0012774	chromosome 15q13.3 microdeletion syndrome	skos:exactMatch	DOID:0060394	chromosome 15q13.3 microdeletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012783	RFT1-congenital disorder of glycosylation	skos:exactMatch	DOID:0080566	congenital disorder of glycosylation In	semapv:ManualMappingCuration	2023-03-17
MONDO:0012784	autosomal recessive ataxia due to ubiquinone deficiency	skos:exactMatch	DOID:0070241	primary coenzyme Q10 deficiency 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012786	juvenile cataract-microcornea-renal glucosuria syndrome	skos:exactMatch	DOID:0070353	cataract 47	semapv:ManualMappingCuration	2023-03-17
MONDO:0012787	hereditary spastic paraplegia 39	skos:exactMatch	DOID:0110790	hereditary spastic paraplegia 39	semapv:ManualMappingCuration	2023-03-17
MONDO:0012789	dystonia 16	skos:exactMatch	DOID:0090048	dystonia 16	semapv:ManualMappingCuration	2023-03-17
MONDO:0012791	mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria	skos:exactMatch	DOID:0080124	mitochondrial DNA depletion syndrome 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0012792	mitochondrial DNA depletion syndrome 8a	skos:exactMatch	DOID:0070331	mitochondrial DNA depletion syndrome 8b	semapv:ManualMappingCuration	2023-06-18
MONDO:0012792	mitochondrial DNA depletion syndrome 8a	skos:exactMatch	DOID:0080127	mitochondrial DNA depletion syndrome 8A	semapv:ManualMappingCuration	2023-03-17
MONDO:0012794	ANE syndrome	skos:exactMatch	DOID:0112244	alopecia, neurologic defects, and endocrinopathy syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0012796	retinitis pigmentosa 41	skos:exactMatch	DOID:0110376	retinitis pigmentosa 41	semapv:ManualMappingCuration	2024-04-21
MONDO:0012799	hypertrophic cardiomyopathy 11	skos:exactMatch	DOID:0110317	hypertrophic cardiomyopathy 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0012802	oculoauricular syndrome	skos:exactMatch	DOID:0060482	oculoauricular syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012804	hypertrophic cardiomyopathy 12	skos:exactMatch	DOID:0110318	hypertrophic cardiomyopathy 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0012805	childhood onset GLUT1 deficiency syndrome 2	skos:exactMatch	DOID:0090045	glucose transporter type 1 deficiency syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012806	ectodermal dysplasia and immunodeficiency 2	skos:exactMatch	DOID:0081079	ectodermal dysplasia and immunodeficiency 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0012808	dilated cardiomyopathy 1AA	skos:exactMatch	DOID:0110428	dilated cardiomyopathy 1AA	semapv:ManualMappingCuration	2024-02-18
MONDO:0012812	developmental and epileptic encephalopathy, 4	skos:exactMatch	DOID:0080436	developmental and epileptic encephalopathy 4	semapv:ManualMappingCuration	2024-02-18
MONDO:0012824	hypomyelinating leukodystrophy 4	skos:exactMatch	DOID:0060789	hypomyelinating leukodystrophy 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0012825	extraskeletal myxoid chondrosarcoma	skos:exactMatch	DOID:6496	extraskeletal myxoid chondrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0012830	chromosome 10q23 deletion syndrome	skos:exactMatch	DOID:0060389	chromosome 10q23 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012833	Crouzon syndrome-acanthosis nigricans syndrome	skos:exactMatch	DOID:0111161	Crouzon syndrome-acanthosis nigricans syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012850	hypophosphatemic nephrolithiasis/osteoporosis 1	skos:exactMatch	DOID:0080077	hypophosphatemic nephrolithiasis/osteoporosis 1	semapv:ManualMappingCuration	2024-02-18
MONDO:0012851	hypophosphatemic nephrolithiasis/osteoporosis 2	skos:exactMatch	DOID:0080078	hypophosphatemic nephrolithiasis/osteoporosis 2	semapv:ManualMappingCuration	2024-02-18
MONDO:0012856	Birk-Barel syndrome	skos:exactMatch	DOID:0050675	Birk-Barel syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012859	autosomal recessive osteopetrosis 7	skos:exactMatch	DOID:0110946	autosomal recessive osteopetrosis 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0012864	chromosome 2q32-q33 deletion syndrome	skos:exactMatch	DOID:0060428	SATB2-associated syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012866	hereditary spastic paraplegia 35	skos:exactMatch	DOID:0110786	hereditary spastic paraplegia 35	semapv:ManualMappingCuration	2023-03-17
MONDO:0012867	hereditary spastic paraplegia 38	skos:exactMatch	DOID:0110789	hereditary spastic paraplegia 38	semapv:ManualMappingCuration	2023-03-17
MONDO:0012868	thrombophilia due to protein S deficiency, autosomal dominant	skos:exactMatch	DOID:0111900	autosomal dominant thrombophilia due to protein S deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0012873	Ehlers-Danlos syndrome, spondylocheirodysplastic type	skos:exactMatch	DOID:0080739	Ehlers-Danlos syndrome spondylodysplastic type 3	semapv:ManualMappingCuration	2023-06-18
MONDO:0012876	heparin cofactor 2 deficiency	skos:exactMatch	DOID:0111901	heparin cofactor II deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0012880	hypogonadotropic hypogonadism 5 with or without anosmia	skos:exactMatch	DOID:0090084	hypogonadotropic hypogonadism 5 with or without anosmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0012885	SRD5A3-congenital disorder of glycosylation	skos:exactMatch	DOID:0080568	congenital disorder of glycosylation Iq	semapv:ManualMappingCuration	2023-03-17
MONDO:0012895	torsion dystonia 17	skos:exactMatch	DOID:0090042	torsion dystonia 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0012897	congenital factor XI deficiency	skos:exactMatch	DOID:2229	factor XI deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012900	cardiomyopathy, familial restrictive, 3	skos:exactMatch	DOID:0111427	restrictive cardiomyopathy 3	semapv:ManualMappingCuration	2024-02-18
MONDO:0012905	hypomyelinating leukodystrophy 6	skos:exactMatch	DOID:0060798	hypomyelinating leukodystrophy 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0012912	pseudopseudohypoparathyroidism	skos:exactMatch	DOID:4183	pseudopseudohypoparathyroidism	semapv:ManualMappingCuration	2023-03-17
MONDO:0012914	chromosome 1q21.1 deletion syndrome	skos:exactMatch	DOID:0060411	chromosome 1q21.1 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012915	chromosome 1q21.1 duplication syndrome	skos:exactMatch	DOID:0060435	chromosome 1q21.1 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012916	chromosome 2p16.1-p15 deletion syndrome	skos:exactMatch	DOID:0060415	chromosome 2p16.1-p15 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012919	type 1 diabetes mellitus 20	skos:exactMatch	DOID:0110757	type 1 diabetes mellitus 20	semapv:ManualMappingCuration	2023-04-17
MONDO:0012921	type 1 diabetes mellitus 22	skos:exactMatch	DOID:0110759	type 1 diabetes mellitus 22	semapv:ManualMappingCuration	2023-11-19
MONDO:0012923	congenital generalized lipodystrophy type 3	skos:exactMatch	DOID:0111137	congenital generalized lipodystrophy type 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0012927	chromosome 1q41-q42 deletion syndrome	skos:exactMatch	DOID:0060412	chromosome 1q41-q42 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012928	hereditary spastic paraplegia 42	skos:exactMatch	DOID:0110794	hereditary spastic paraplegia 42	semapv:ManualMappingCuration	2023-03-17
MONDO:0012929	Compton-North congenital myopathy	skos:exactMatch	DOID:0080101	Compton-North congenital myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0012930	autosomal recessive severe congenital neutropenia due to G6PC3 deficiency	skos:exactMatch	DOID:0112136	severe congenital neutropenia 4	semapv:ManualMappingCuration	2023-04-17
MONDO:0012941	inflammatory bowel disease 25	skos:exactMatch	DOID:0110909	inflammatory bowel disease 25	semapv:ManualMappingCuration	2023-03-17
MONDO:0012945	amyotrophic lateral sclerosis type 11	skos:exactMatch	DOID:0060202	amyotrophic lateral sclerosis type 11	semapv:ManualMappingCuration	2024-04-21
MONDO:0012947	intellectual disability, autosomal dominant 4	skos:exactMatch	DOID:0070034	autosomal dominant intellectual developmental disorder 4	semapv:ManualMappingCuration	2023-11-19
MONDO:0012948	chromosome 6pter-p24 deletion syndrome	skos:exactMatch	DOID:0060422	chromosome 6pter-p24 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012960	intellectual disability, autosomal dominant 5	skos:exactMatch	DOID:0070035	autosomal dominant intellectual developmental disorder 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0012964	chromosome 15q26-qter deletion syndrome	skos:exactMatch	DOID:0060397	chromosome 15q26-qter deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012975	autosomal dominant nonsyndromic hearing loss 3B	skos:exactMatch	DOID:0110565	autosomal dominant nonsyndromic deafness 3B	semapv:ManualMappingCuration	2024-04-21
MONDO:0012977	autosomal recessive nonsyndromic hearing loss 1B	skos:exactMatch	DOID:0110476	autosomal recessive nonsyndromic deafness 1B	semapv:ManualMappingCuration	2024-04-21
MONDO:0012980	endocrine-cerebro-osteodysplasia syndrome	skos:exactMatch	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012981	hereditary spherocytosis type 4	skos:exactMatch	DOID:0110919	hereditary spherocytosis type 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0012982	episodic ataxia type 6	skos:exactMatch	DOID:0050994	episodic ataxia type 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0012983	cone-rod dystrophy 12	skos:exactMatch	DOID:0111019	cone-rod dystrophy 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0012984	PHARC syndrome	skos:exactMatch	DOID:0080181	PHARC syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012986	bilateral parasagittal parieto-occipital polymicrogyria	skos:exactMatch	DOID:0080923	bilateral parasagittal parieto-occipital polymicrogyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0012988	hypogonadotropic hypogonadism 6 with or without anosmia	skos:exactMatch	DOID:0090086	hypogonadotropic hypogonadism 6 with or without anosmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0012991	Kahrizi syndrome	skos:exactMatch	DOID:0050807	Kahrizi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0012994	dopa-responsive dystonia due to sepiapterin reductase deficiency	skos:exactMatch	DOID:0111168	sepiapterin reductase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012996	AGAT deficiency	skos:exactMatch	DOID:0050712	AGAT deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0012999	guanidinoacetate methyltransferase deficiency	skos:exactMatch	DOID:0050799	guanidinoacetate methyltransferase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013005	EAST syndrome	skos:exactMatch	DOID:0060484	EAST syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013006	isolated growth hormone deficiency type IB	skos:exactMatch	DOID:0060874	isolated growth hormone deficiency type IB	semapv:ManualMappingCuration	2023-03-17
MONDO:0013007	combined immunodeficiency due to ORAI1 deficiency	skos:exactMatch	DOID:0111976	immunodeficiency 9	semapv:ManualMappingCuration	2023-04-17
MONDO:0013008	combined immunodeficiency due to STIM1 deficiency	skos:exactMatch	DOID:0111970	immunodeficiency 10	semapv:ManualMappingCuration	2023-04-17
MONDO:0013011	atrial septal defect 5	skos:exactMatch	DOID:0110110	atrial heart septal defect 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0013016	leukocyte adhesion deficiency 3	skos:exactMatch	DOID:0110912	leukocyte adhesion deficiency 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013017	hypotrichosis 5	skos:exactMatch	DOID:0110702	hypotrichosis 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0013025	chromosome 6q24-q25 deletion syndrome	skos:exactMatch	DOID:0060424	chromosome 6q24-q25 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013026	subepithelial mucinous corneal dystrophy	skos:exactMatch	DOID:0060454	subepithelial mucinous corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0013027	posterior amorphous corneal dystrophy	skos:exactMatch	DOID:0060452	posterior amorphous corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0013030	dilated cardiomyopathy 1BB	skos:exactMatch	DOID:0110458	dilated cardiomyopathy 1BB	semapv:ManualMappingCuration	2024-02-18
MONDO:0013032	epilepsy, idiopathic generalized, susceptibility to, 8	skos:exactMatch	DOID:0111322	idiopathic generalized epilepsy 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0013034	keratosis palmoplantaris striata 2	skos:exactMatch	DOID:0081109	keratosis palmoplantaris striata 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0013035	orofaciodigital syndrome XI	skos:exactMatch	DOID:0060381	orofaciodigital syndrome XI	semapv:ManualMappingCuration	2023-03-17
MONDO:0013038	CLOVES syndrome	skos:exactMatch	DOID:0080351	CLOVES syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013051	autosomal recessive cutis laxa type 2B	skos:exactMatch	DOID:0070137	autosomal recessive cutis laxa type IIB	semapv:ManualMappingCuration	2023-03-17
MONDO:0013056	developmental and epileptic encephalopathy, 39	skos:exactMatch	DOID:0080349	developmental and epileptic encephalopathy 39	semapv:ManualMappingCuration	2023-03-17
MONDO:0013058	cystic leukoencephalopathy without megalencephaly	skos:exactMatch	DOID:0081007	RNASET2-deficient cystic leukoencephalopathy	semapv:ManualMappingCuration	2023-04-17
MONDO:0013060	autosomal recessive Parkinson disease 14	skos:exactMatch	DOID:0060900	Parkinson's disease 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0013061	myofibrillar myopathy 6	skos:exactMatch	DOID:0080097	myofibrillar myopathy 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0013062	long QT syndrome 12	skos:exactMatch	DOID:0110653	long QT syndrome 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0013065	premature ovarian failure 7	skos:exactMatch	DOID:0080864	primary ovarian insufficiency 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0013066	46,XY sex reversal 3	skos:exactMatch	DOID:0111772	46,XY sex reversal 3	semapv:ManualMappingCuration	2023-11-19
MONDO:0013067	cataract 34 multiple types	skos:exactMatch	DOID:0110230	cataract 34 multiple types	semapv:ManualMappingCuration	2024-04-21
MONDO:0013069	autosomal recessive optic atrophy, OPA7 type	skos:exactMatch	DOID:0111437	optic atrophy 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0013070	spermatogenic failure 7	skos:exactMatch	DOID:0070173	spermatogenic failure 7	semapv:ManualMappingCuration	2024-02-18
MONDO:0013071	Emery-Dreifuss muscular dystrophy 4, autosomal dominant	skos:exactMatch	DOID:0070249	autosomal dominant Emery-Dreifuss muscular dystrophy 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0013081	lymphoproliferative syndrome 1	skos:exactMatch	DOID:0060707	lymphoproliferative syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0013090	chromosome 19q13.11 deletion syndrome	skos:exactMatch	DOID:0060408	chromosome 19q13.11 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013110	neurodegenerative syndrome due to cerebral folate transport deficiency	skos:exactMatch	DOID:0050719	cerebral folate receptor alpha deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013111	acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins	skos:exactMatch	DOID:0080778	transient infantile liver failure	semapv:ManualMappingCuration	2023-04-17
MONDO:0013112	bronchiectasis with or without elevated sweat chloride 3	skos:exactMatch	DOID:0080528	bronchiectasis 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0013117	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5	skos:exactMatch	DOID:0111518	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0013127	asphyxiating thoracic dystrophy 3	skos:exactMatch	DOID:0050549	Saldino-Noonan syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013127	asphyxiating thoracic dystrophy 3	skos:exactMatch	DOID:0110087	asphyxiating thoracic dystrophy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013130	isolated microphthalmia 4	skos:exactMatch	DOID:0060836	isolated microphthalmia 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0013131	polycystic kidney disease 2	skos:exactMatch	DOID:0110859	polycystic kidney disease 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013132	hereditary spastic paraplegia 36	skos:exactMatch	DOID:0110787	hereditary spastic paraplegia 36	semapv:ManualMappingCuration	2023-03-17
MONDO:0013139	neutropenia, severe congenital, 2, autosomal dominant	skos:exactMatch	DOID:0112131	severe congenital neutropenia 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0013143	hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency	skos:exactMatch	DOID:0111903	thrombophilia due to HRG deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0013144	hereditary antithrombin deficiency	skos:exactMatch	DOID:3755	antithrombin III deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013147	dilated cardiomyopathy 1CC	skos:exactMatch	DOID:0110424	dilated cardiomyopathy 1CC	semapv:ManualMappingCuration	2024-02-18
MONDO:0013148	Brugada syndrome 8	skos:exactMatch	DOID:0110225	Brugada syndrome 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0013154	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2	skos:exactMatch	DOID:0111240	congenital muscular dystrophy-dystroglycanopathy type A2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013155	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3	skos:exactMatch	DOID:0112378	muscular dystrophy-dystroglycanopathy type B3	semapv:ManualMappingCuration	2023-06-18
MONDO:0013156	muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4	skos:exactMatch	DOID:0112379	muscular dystrophy-dystroglycanopathy type B4	semapv:ManualMappingCuration	2023-06-18
MONDO:0013157	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5	skos:exactMatch	DOID:0111241	congenital muscular dystrophy-dystroglycanopathy type A5	semapv:ManualMappingCuration	2023-03-17
MONDO:0013158	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6	skos:exactMatch	DOID:0111242	congenital muscular dystrophy-dystroglycanopathy type A6	semapv:ManualMappingCuration	2023-03-17
MONDO:0013159	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1	skos:exactMatch	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1	semapv:ManualMappingCuration	2023-08-20
MONDO:0013160	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2	skos:exactMatch	DOID:0112380	muscular dystrophy-dystroglycanopathy type B2	semapv:ManualMappingCuration	2023-06-18
MONDO:0013161	autosomal recessive limb-girdle muscular dystrophy type 2O	skos:exactMatch	DOID:0110292	autosomal recessive limb-girdle muscular dystrophy type 2O	semapv:ManualMappingCuration	2023-03-17
MONDO:0013162	autosomal recessive limb-girdle muscular dystrophy type 2N	skos:exactMatch	DOID:0110298	autosomal recessive limb-girdle muscular dystrophy type 2N	semapv:ManualMappingCuration	2023-03-17
MONDO:0013165	hereditary spastic paraplegia 45	skos:exactMatch	DOID:0110797	hereditary spastic paraplegia 45	semapv:ManualMappingCuration	2023-03-17
MONDO:0013166	GABA aminotransaminase deficiency	skos:exactMatch	DOID:0060174	GABA aminotransferase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013168	dilated cardiomyopathy 1DD	skos:exactMatch	DOID:0110447	dilated cardiomyopathy 1DD	semapv:ManualMappingCuration	2024-02-18
MONDO:0013169	chromosome 5p13 duplication syndrome	skos:exactMatch	DOID:0060460	chromosome 5p13 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013170	cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies	skos:exactMatch	DOID:0070139	autosomal recessive cutis laxa type IC	semapv:ManualMappingCuration	2023-03-17
MONDO:0013171	purine nucleoside phosphorylase deficiency	skos:exactMatch	DOID:5813	purine nucleoside phosphorylase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013173	intellectual disability, autosomal recessive 13	skos:exactMatch	DOID:0081098	autosomal recessive intellectual developmental disorder 13	semapv:ManualMappingCuration	2023-06-18
MONDO:0013175	retinitis pigmentosa 50	skos:exactMatch	DOID:0110396	retinitis pigmentosa 50	semapv:ManualMappingCuration	2024-04-21
MONDO:0013177	congenital muscular dystrophy due to integrin alpha-7 deficiency	skos:exactMatch	DOID:0110639	congenital muscular dystrophy due to integrin alpha-7 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013178	congenital muscular dystrophy due to LMNA mutation	skos:exactMatch	DOID:0110640	congenital muscular dystrophy due to LMNA mutation	semapv:ManualMappingCuration	2023-03-17
MONDO:0013179	hereditary spastic paraplegia 44	skos:exactMatch	DOID:0110796	hereditary spastic paraplegia 44	semapv:ManualMappingCuration	2023-03-17
MONDO:0013182	chromosome 17p13.3 duplication syndrome	skos:exactMatch	DOID:0060432	chromosome 17p13.3 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013184	congenital diarrhea 5 with tufting enteropathy	skos:exactMatch	DOID:0060776	congenital diarrhea 5 with tufting enteropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0013186	Noonan syndrome 6	skos:exactMatch	DOID:0060584	Noonan syndrome 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0013189	trichotillomania	skos:exactMatch	DOID:0050587	trichotillomania	semapv:ManualMappingCuration	2023-11-19
MONDO:0013191	focal segmental glomerulosclerosis 5	skos:exactMatch	DOID:0111130	focal segmental glomerulosclerosis 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0013195	hypertrophic cardiomyopathy 13	skos:exactMatch	DOID:0110319	hypertrophic cardiomyopathy 13	semapv:ManualMappingCuration	2023-04-17
MONDO:0013196	Lynch syndrome 8	skos:exactMatch	DOID:0070270	hereditary nonpolyposis colorectal cancer type 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0013197	hypertrophic cardiomyopathy 14	skos:exactMatch	DOID:0110320	hypertrophic cardiomyopathy 14	semapv:ManualMappingCuration	2024-04-21
MONDO:0013198	dilated cardiomyopathy 1EE	skos:exactMatch	DOID:0110453	dilated cardiomyopathy 1EE	semapv:ManualMappingCuration	2024-02-18
MONDO:0013200	hypertrophic cardiomyopathy 15	skos:exactMatch	DOID:0110321	hypertrophic cardiomyopathy 15	semapv:ManualMappingCuration	2024-04-21
MONDO:0013208	cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome	skos:exactMatch	DOID:0080536	hypermanganesemia with dystonia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0013211	dilated cardiomyopathy 1FF	skos:exactMatch	DOID:0110459	dilated cardiomyopathy 1FF	semapv:ManualMappingCuration	2024-02-18
MONDO:0013212	Charcot-Marie-Tooth disease axonal type 2N	skos:exactMatch	DOID:0110177	Charcot-Marie-Tooth disease axonal type 2N	semapv:ManualMappingCuration	2023-03-17
MONDO:0013220	hemochromatosis type 2B	skos:exactMatch	DOID:0111032	hemochromatosis type 2B	semapv:ManualMappingCuration	2023-03-17
MONDO:0013222	Miyoshi muscular dystrophy 3	skos:exactMatch	DOID:0070201	Miyoshi muscular dystrophy 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013223	autosomal recessive spondylometaphyseal dysplasia, Megarbane type	skos:exactMatch	DOID:0112304	spondylometaphyseal dysplasia Megarbane-Dagher-Melike type	semapv:ManualMappingCuration	2023-06-18
MONDO:0013225	congenital generalized lipodystrophy type 4	skos:exactMatch	DOID:0111138	congenital generalized lipodystrophy type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0013238	chromosome 17q23.1-q23.2 deletion syndrome	skos:exactMatch	DOID:0060405	chromosome 17q23.1-q23.2 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013239	hereditary spastic paraplegia 41	skos:exactMatch	DOID:0110793	hereditary spastic paraplegia 41	semapv:ManualMappingCuration	2023-03-17
MONDO:0013240	maturity-onset diabetes of the young type 10	skos:exactMatch	DOID:0111108	maturity-onset diabetes of the young type 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0013241	spinocerebellar ataxia type 30	skos:exactMatch	DOID:0050979	spinocerebellar ataxia type 30	semapv:ManualMappingCuration	2023-03-17
MONDO:0013247	Fanconi renotubular syndrome 2	skos:exactMatch	DOID:0080758	Fanconi renotubular syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0013252	Warsaw breakage syndrome	skos:exactMatch	DOID:0060535	Warsaw breakage syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013254	microcephaly, seizures, and developmental delay	skos:exactMatch	DOID:0080457	microcephaly, seizures, and developmental delay	semapv:ManualMappingCuration	2023-03-17
MONDO:0013256	chromosome 15q24 deletion syndrome	skos:exactMatch	DOID:0060395	chromosome 15q24 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013266	intellectual disability, autosomal dominant 20	skos:exactMatch	DOID:0070050	neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language	semapv:ManualMappingCuration	2024-08-18
MONDO:0013267	distal 16p11.2 microdeletion syndrome	skos:exactMatch	DOID:0060398	chromosome 16p11.2 deletion syndrome, 220-kb	semapv:ManualMappingCuration	2023-03-17
MONDO:0013268	frontonasal dysplasia with alopecia and genital anomaly	skos:exactMatch	DOID:0081046	frontonasal dysplasia 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0013271	frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome	skos:exactMatch	DOID:0081047	frontonasal dysplasia 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0013272	chromosome 14q11-q22 deletion syndrome	skos:exactMatch	DOID:0060392	chromosome 14q11-q22 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013273	chromosome 16p13.3 duplication syndrome	skos:exactMatch	DOID:0060431	chromosome 16p13.3 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013278	lymphatic malformation 3	skos:exactMatch	DOID:0070208	hereditary lymphedema IC	semapv:ManualMappingCuration	2024-04-21
MONDO:0013279	long QT syndrome 13	skos:exactMatch	DOID:0110654	long QT syndrome 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0013281	COG4-congenital disorder of glycosylation	skos:exactMatch	DOID:0070262	congenital disorder of glycosylation type IIj	semapv:ManualMappingCuration	2023-03-17
MONDO:0013282	alpha 1-antitrypsin deficiency	skos:exactMatch	DOID:13372	alpha 1-antitrypsin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013284	immunodeficiency, common variable, 4	skos:exactMatch	DOID:0081147	common variable immunodeficiency 4	semapv:ManualMappingCuration	2023-06-18
MONDO:0013286	immunodeficiency, common variable, 6	skos:exactMatch	DOID:0081149	common variable immunodeficiency 6	semapv:ManualMappingCuration	2023-06-18
MONDO:0013291	glycogen storage disease XV	skos:exactMatch	DOID:0050579	glycogen storage disease XV	semapv:ManualMappingCuration	2023-03-17
MONDO:0013292	chromosome 4q21 deletion syndrome	skos:exactMatch	DOID:0060420	chromosome 4q21 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013297	autosomal dominant limb-girdle muscular dystrophy type 1H	skos:exactMatch	DOID:0110303	autosomal dominant limb-girdle muscular dystrophy type 1H	semapv:ManualMappingCuration	2023-03-17
MONDO:0013298	chromosome 17q21.31 duplication syndrome	skos:exactMatch	DOID:0060434	chromosome 17q21.31 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013299	chromosome 6q11-q14 deletion syndrome	skos:exactMatch	DOID:0060423	chromosome 6q11-q14 deletion syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0013302	nephronophthisis 11	skos:exactMatch	DOID:0111118	nephronophthisis 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0013304	von Willebrand disease 2	skos:exactMatch	DOID:0060574	von Willebrand's disease 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013306	combined oxidative phosphorylation defect type 7	skos:exactMatch	DOID:0111487	combined oxidative phosphorylation deficiency 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0013310	congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency	skos:exactMatch	DOID:0080925	cytochrome P450 oxidoreductase deficiency	semapv:ManualMappingCuration	2023-06-18
MONDO:0013316	occult macular dystrophy	skos:exactMatch	DOID:0050578	occult macular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0013320	chromosome 16p12.2-p11.2 deletion syndrome	skos:exactMatch	DOID:0060400	chromosome 16p12.2-p11.2 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013325	COG5-congenital disorder of glycosylation	skos:exactMatch	DOID:0070261	congenital disorder of glycosylation type IIi	semapv:ManualMappingCuration	2023-03-17
MONDO:0013327	primary hyperoxaluria type 3	skos:exactMatch	DOID:0111672	primary hyperoxaluria type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013334	cocoon syndrome	skos:exactMatch	DOID:0060647	fetal encasement syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013336	chromosome 19p13.13 deletion syndrome	skos:exactMatch	DOID:0060426	chromosome 19p13.13 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013338	Charcot-Marie-Tooth disease recessive intermediate B	skos:exactMatch	DOID:0110204	Charcot-Marie-Tooth disease recessive intermediate B	semapv:ManualMappingCuration	2023-03-17
MONDO:0013339	dilated cardiomyopathy 1GG	skos:exactMatch	DOID:0110435	dilated cardiomyopathy 1GG	semapv:ManualMappingCuration	2024-02-18
MONDO:0013341	methylmalonic acidemia due to transcobalamin receptor defect	skos:exactMatch	DOID:0060741	methylmalonic acidemia due to transcobalamin receptor defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0013342	hereditary spastic paraplegia 48	skos:exactMatch	DOID:0110800	hereditary spastic paraplegia 48	semapv:ManualMappingCuration	2023-03-17
MONDO:0013349	ALG11-congenital disorder of glycosylation	skos:exactMatch	DOID:0080567	congenital disorder of glycosylation Ip	semapv:ManualMappingCuration	2023-03-17
MONDO:0013351	infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	skos:exactMatch	DOID:0111262	infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0013352	intellectual disability-severe speech delay-mild dysmorphism syndrome	skos:exactMatch	DOID:0111331	intellectual disability-severe speech delay-mild dysmorphism syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013354	spastic ataxia 4	skos:exactMatch	DOID:0050943	spastic ataxia 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0013355	congenital dyserythropoietic anemia type 4	skos:exactMatch	DOID:0111400	congenital dyserythropoietic anemia type IV	semapv:ManualMappingCuration	2023-03-17
MONDO:0013357	chromosome 17q11.2 deletion syndrome, 1.4Mb	skos:exactMatch	DOID:0060403	chromosome 17q11.2 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013361	congenital prothrombin deficiency	skos:exactMatch	DOID:2235	prothrombin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013363	chromosome 2q31.1 duplication syndrome	skos:exactMatch	DOID:0060458	chromosome 2q31.1 duplication syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0013369	hypertrophic cardiomyopathy 7	skos:exactMatch	DOID:0110313	hypertrophic cardiomyopathy 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0013371	dilated cardiomyopathy 1U	skos:exactMatch	DOID:0110455	dilated cardiomyopathy 1U	semapv:ManualMappingCuration	2024-02-18
MONDO:0013372	long QT syndrome 5	skos:exactMatch	DOID:0110647	long QT syndrome 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0013373	dilated cardiomyopathy 1V	skos:exactMatch	DOID:0110427	dilated cardiomyopathy 1V	semapv:ManualMappingCuration	2024-02-18
MONDO:0013375	Klippel-Feil syndrome 3, autosomal dominant	skos:exactMatch	DOID:0080591	Klippel-Feil syndrome 3	semapv:ManualMappingCuration	2024-02-18
MONDO:0013377	isolated microphthalmia 7	skos:exactMatch	DOID:0060838	isolated microphthalmia 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0013378	orofacial cleft 10	skos:exactMatch	DOID:0080403	orofacial cleft 10	semapv:ManualMappingCuration	2023-11-19
MONDO:0013389	developmental and epileptic encephalopathy, 12	skos:exactMatch	DOID:0080459	developmental and epileptic encephalopathy 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0013390	autosomal recessive limb-girdle muscular dystrophy type 2Q	skos:exactMatch	DOID:0110285	autosomal recessive limb-girdle muscular dystrophy type 2Q	semapv:ManualMappingCuration	2023-03-17
MONDO:0013392	autosomal recessive spinocerebellar ataxia 10	skos:exactMatch	DOID:0050999	autosomal recessive spinocerebellar ataxia 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0013396	chromosome 1p32-p31 deletion syndrome	skos:exactMatch	DOID:0060409	NFIA-related disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0013400	Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency	skos:exactMatch	DOID:0050546	congenital adrenal insufficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013401	hereditary spastic paraplegia 51	skos:exactMatch	DOID:0110803	hereditary spastic paraplegia 51	semapv:ManualMappingCuration	2024-04-21
MONDO:0013404	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase	skos:exactMatch	DOID:0111039	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase	semapv:ManualMappingCuration	2023-03-17
MONDO:0013409	age related macular degeneration 5	skos:exactMatch	DOID:0110028	age related macular degeneration 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0013410	46,XY sex reversal 6	skos:exactMatch	DOID:0111769	46,XY sex reversal 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0013411	cataract 16 multiple types	skos:exactMatch	DOID:0110250	cataract 16 multiple types	semapv:ManualMappingCuration	2023-03-17
MONDO:0013412	hypertrophic cardiomyopathy 9	skos:exactMatch	DOID:0110315	hypertrophic cardiomyopathy 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0013415	chromosome 17p13.1 deletion syndrome	skos:exactMatch	DOID:0060402	chromosome 17p13.1 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013417	complement component 3 deficiency	skos:exactMatch	DOID:8354	complement component 3 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013420	age related macular degeneration 12	skos:exactMatch	DOID:0110024	age related macular degeneration 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0013421	type II complement component 8 deficiency	skos:exactMatch	DOID:0060302	type II complement component 8 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013424	3p- syndrome	skos:exactMatch	DOID:0060417	3p deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013426	aneurysm-osteoarthritis syndrome	skos:exactMatch	DOID:0070237	Loeys-Dietz syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013427	immunodeficiency 31B	skos:exactMatch	DOID:0111944	immunodeficiency 31B	semapv:ManualMappingCuration	2023-03-17
MONDO:0013439	congenital bile acid synthesis defect 3	skos:exactMatch	DOID:0111070	congenital bile acid synthesis defect 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013440	autosomal recessive limb-girdle muscular dystrophy type 2P	skos:exactMatch	DOID:0110293	autosomal recessive limb-girdle muscular dystrophy type 2P	semapv:ManualMappingCuration	2023-03-17
MONDO:0013453	Leber congenital amaurosis 8	skos:exactMatch	DOID:0110079	Leber congenital amaurosis 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0013459	osteogenesis imperfecta type 10	skos:exactMatch	DOID:0110346	osteogenesis imperfecta type 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0013463	congenital heart defects, multiple types, 6	skos:exactMatch	DOID:0060772	multiple types of congenital heart defects 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0013464	episodic ataxia type 5	skos:exactMatch	DOID:0050993	episodic ataxia type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0013470	generalized epilepsy with febrile seizures plus, type 7	skos:exactMatch	DOID:0111295	generalized epilepsy with febrile seizures plus 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0013472	fatal infantile hypertonic myofibrillar myopathy	skos:exactMatch	DOID:0080309	fatal infantile hypertonic myofibrillar myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0013474	hypertrophic cardiomyopathy 17	skos:exactMatch	DOID:0110323	hypertrophic cardiomyopathy 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0013477	hypertrophic cardiomyopathy 20	skos:exactMatch	DOID:0110326	hypertrophic cardiomyopathy 20	semapv:ManualMappingCuration	2023-03-17
MONDO:0013478	PLIN1-related familial partial lipodystrophy	skos:exactMatch	DOID:0070205	familial partial lipodystrophy type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0013479	dilated cardiomyopathy 1HH	skos:exactMatch	DOID:0110448	dilated cardiomyopathy 1HH	semapv:ManualMappingCuration	2024-02-18
MONDO:0013481	chromosome 13q14 deletion syndrome	skos:exactMatch	DOID:0060391	chromosome 13q14 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013485	spinocerebellar ataxia type 35	skos:exactMatch	DOID:0050982	spinocerebellar ataxia type 35	semapv:ManualMappingCuration	2023-03-17
MONDO:0013489	autosomal recessive nonsyndromic hearing loss 89	skos:exactMatch	DOID:0110534	autosomal recessive nonsyndromic deafness 89	semapv:ManualMappingCuration	2024-04-21
MONDO:0013498	schizophrenia 15	skos:exactMatch	DOID:0070091	schizophrenia 15	semapv:ManualMappingCuration	2024-04-21
MONDO:0013499	Fanconi anemia complementation group P	skos:exactMatch	DOID:0111092	Fanconi anemia complementation group P	semapv:ManualMappingCuration	2023-03-17
MONDO:0013500	immunodeficiency 51	skos:exactMatch	DOID:0111996	immunodeficiency 51	semapv:ManualMappingCuration	2023-03-17
MONDO:0013501	frontotemporal dementia and/or amyotrophic lateral sclerosis 6	skos:exactMatch	DOID:0060205	frontotemporal dementia and/or amyotrophic lateral sclerosis 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0013504	spermatogenic failure 8	skos:exactMatch	DOID:0070169	spermatogenic failure 8	semapv:ManualMappingCuration	2024-02-18
MONDO:0013512	hemoglobin H disease	skos:exactMatch	DOID:0110031	hemoglobin H disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0013514	hypotrichosis 3	skos:exactMatch	DOID:0110700	hypotrichosis 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0013521	dyskeratosis congenita, autosomal dominant 2	skos:exactMatch	DOID:0070016	autosomal dominant dyskeratosis congenita 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013522	dyskeratosis congenita, autosomal dominant 3	skos:exactMatch	DOID:0070018	autosomal dominant dyskeratosis congenita 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013523	Nestor-Guillermo progeria syndrome	skos:exactMatch	DOID:0081334	Nestor-Guillermo progeria syndrome	semapv:ManualMappingCuration	2023-05-21
MONDO:0013526	progressive myoclonic epilepsy type 6	skos:exactMatch	DOID:0111449	progressive myoclonus epilepsy 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0013527	lissencephaly 4	skos:exactMatch	DOID:0112235	lissencephaly 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0013531	PSPH deficiency	skos:exactMatch	DOID:0050724	PSPH deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013534	apolipoprotein c-III deficiency	skos:exactMatch	DOID:0111370	apolipoprotein C-III deficiency	semapv:ManualMappingCuration	2023-11-19
MONDO:0013541	complex cortical dysplasia with other brain malformations 1	skos:exactMatch	DOID:0090137	complex cortical dysplasia with other brain malformations 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0013546	mitochondrial complex V (ATP synthase) deficiency nuclear type 2	skos:exactMatch	DOID:0060331	mitochondrial complex V (ATP synthase) deficiency nuclear type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013547	mitochondrial complex V (ATP synthase) deficiency nuclear type 3	skos:exactMatch	DOID:0060332	mitochondrial complex V (ATP synthase) deficiency nuclear type 3	semapv:ManualMappingCuration	2023-11-19
MONDO:0013550	distal myopathy with posterior leg and anterior hand involvement	skos:exactMatch	DOID:0111190	distal myopathy 4	semapv:ManualMappingCuration	2023-04-17
MONDO:0013555	Hermansky-Pudlak syndrome 3	skos:exactMatch	DOID:0060541	Hermansky-Pudlak syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0013559	Hermansky-Pudlak syndrome 7	skos:exactMatch	DOID:0060545	Hermansky-Pudlak syndrome 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0013560	Hermansky-Pudlak syndrome 8	skos:exactMatch	DOID:0060546	Hermansky-Pudlak syndrome 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0013561	chondrodysplasia with joint dislocations, gPAPP type	skos:exactMatch	DOID:0112224	chondrodysplasia with joint dislocations gPAPP type	semapv:ManualMappingCuration	2023-04-17
MONDO:0013563	multiple congenital anomalies-hypotonia-seizures syndrome 1	skos:exactMatch	DOID:0080138	multiple congenital anomalies-hypotonia-seizures syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0013566	Fanconi anemia complementation group L	skos:exactMatch	DOID:0111082	Fanconi anemia complementation group L	semapv:ManualMappingCuration	2023-03-17
MONDO:0013567	atrial septal defect 3	skos:exactMatch	DOID:0110108	atrial heart septal defect 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0013570	combined oxidative phosphorylation defect type 8	skos:exactMatch	DOID:0111479	combined oxidative phosphorylation deficiency 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0013578	DYRK1A-related intellectual disability syndrome	skos:exactMatch	DOID:0070037	autosomal dominant intellectual developmental disorder 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0013581	intellectual disability, autosomal dominant 2	skos:exactMatch	DOID:0070032	autosomal dominant intellectual developmental disorder 2	semapv:ManualMappingCuration	2023-11-19
MONDO:0013584	hereditary sensory neuropathy-deafness-dementia syndrome	skos:exactMatch	DOID:0070158	hereditary sensory neuropathy type 1E	semapv:ManualMappingCuration	2023-03-17
MONDO:0013585	hydrolethalus syndrome 2	skos:exactMatch	DOID:0111356	hydrolethalus syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013591	epiphyseal dysplasia, multiple, 6	skos:exactMatch	DOID:0070301	multiple epiphyseal dysplasia 6	semapv:ManualMappingCuration	2023-11-19
MONDO:0013594	spinocerebellar ataxia type 36	skos:exactMatch	DOID:0050983	spinocerebellar ataxia type 36	semapv:ManualMappingCuration	2023-03-17
MONDO:0013597	platelet-type bleeding disorder 14	skos:exactMatch	DOID:0111047	platelet-type bleeding disorder 14	semapv:ManualMappingCuration	2024-04-21
MONDO:0013598	myostatin-related muscle hypertrophy	skos:exactMatch	DOID:0111072	myostatin-related muscle hypertrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0013599	autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome	skos:exactMatch	DOID:0111946	immunodeficiency 31C	semapv:ManualMappingCuration	2023-04-17
MONDO:0013606	Hermansky-Pudlak syndrome 9	skos:exactMatch	DOID:0060547	Hermansky-Pudlak syndrome 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0013607	monocytopenia with susceptibility to infections	skos:exactMatch	DOID:0111947	immunodeficiency 21	semapv:ManualMappingCuration	2023-04-17
MONDO:0013612	geleophysic dysplasia 2	skos:exactMatch	DOID:0111726	geleophysic dysplasia 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0013613	Leber congenital amaurosis 16	skos:exactMatch	DOID:0110118	Leber congenital amaurosis 16	semapv:ManualMappingCuration	2024-04-21
MONDO:0013620	congenital myasthenic syndrome 16	skos:exactMatch	DOID:0110682	congenital myasthenic syndrome 16	semapv:ManualMappingCuration	2024-04-21
MONDO:0013621	LAMB2-related infantile-onset nephrotic syndrome	skos:exactMatch	DOID:0080380	nephrotic syndrome type 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0013622	platelet-type bleeding disorder 9	skos:exactMatch	DOID:0111045	platelet-type bleeding disorder 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0013623	platelet-type bleeding disorder 11	skos:exactMatch	DOID:0111057	platelet-type bleeding disorder 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0013624	Rafiq syndrome	skos:exactMatch	DOID:0081097	Rafiq syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0013626	psoriasis 14, pustular	skos:exactMatch	DOID:0080474	pustular psoriasis 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0013634	neuropathy, hereditary sensory, type 2C	skos:exactMatch	DOID:0070147	hereditary sensory neuropathy type 2C	semapv:ManualMappingCuration	2024-04-21
MONDO:0013644	Charcot-Marie-Tooth disease axonal type 2O	skos:exactMatch	DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O	semapv:ManualMappingCuration	2023-03-17
MONDO:0013645	autosomal recessive spinocerebellar ataxia 11	skos:exactMatch	DOID:0080063	autosomal recessive spinocerebellar ataxia 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0013646	chromosome 8q21.11 deletion syndrome	skos:exactMatch	DOID:0060425	chromosome 8q21.11 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013655	intellectual disability, autosomal dominant 8	skos:exactMatch	DOID:0070038	autosomal dominant intellectual developmental disorder 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0013656	intellectual disability, autosomal dominant 9	skos:exactMatch	DOID:0070039	NESCAV syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013657	intellectual disability, autosomal dominant 10	skos:exactMatch	DOID:0070040	autosomal dominant intellectual developmental disorder 10	semapv:ManualMappingCuration	2023-11-19
MONDO:0013661	combined malonic and methylmalonic acidemia	skos:exactMatch	DOID:0111263	combined malonic and methylmalonic acidemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0013674	neurodegeneration with brain iron accumulation 4	skos:exactMatch	DOID:0110738	neurodegeneration with brain iron accumulation 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0013675	multiple mitochondrial dysfunctions syndrome 2	skos:exactMatch	DOID:0080134	multiple mitochondrial dysfunctions syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013677	Emery-Dreifuss muscular dystrophy 7, autosomal dominant	skos:exactMatch	DOID:0070252	autosomal dominant Emery-Dreifuss muscular dystrophy 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0013679	sclerosteosis 2	skos:exactMatch	DOID:0060757	sclerosteosis 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0013687	autosomal recessive spinocerebellar ataxia 12	skos:exactMatch	DOID:0080060	autosomal recessive spinocerebellar ataxia 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0013690	Pitt-Hopkins-like syndrome 2	skos:exactMatch	DOID:0111332	Pitt-Hopkins-like syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0013702	intellectual disability, autosomal recessive 27	skos:exactMatch	DOID:0081193	autosomal recessive intellectual developmental disorder 27	semapv:ManualMappingCuration	2023-06-18
MONDO:0013721	complement component 4a deficiency	skos:exactMatch	DOID:0060297	complement component 4A deficiency	semapv:ManualMappingCuration	2023-11-19
MONDO:0013722	hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism	skos:exactMatch	DOID:0060797	hypomyelinating leukodystrophy 8	semapv:ManualMappingCuration	2023-11-19
MONDO:0013726	encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1	skos:exactMatch	DOID:0070347	encephalopathy due to defective mitochondrial and peroxisomal fission 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0013730	graft versus host disease	skos:exactMatch	DOID:0081267	graft-versus-host disease	semapv:ManualMappingCuration	2023-04-17
MONDO:0013731	MEGF10-related myopathy	skos:exactMatch	DOID:0111333	early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013737	hereditary spastic paraplegia 46	skos:exactMatch	DOID:0110798	hereditary spastic paraplegia 46	semapv:ManualMappingCuration	2023-03-17
MONDO:0013741	familial temporal lobe epilepsy 5	skos:exactMatch	DOID:0060752	familial temporal lobe epilepsy 5	semapv:ManualMappingCuration	2023-11-19
MONDO:0013750	atrial septal defect 8	skos:exactMatch	DOID:0110113	atrial heart septal defect 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0013751	cutis laxa, autosomal dominant 2	skos:exactMatch	DOID:0070136	autosomal dominant cutis laxa 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0013753	Charcot-Marie-Tooth disease axonal type 2P	skos:exactMatch	DOID:0110169	Charcot-Marie-Tooth disease axonal type 2P	semapv:ManualMappingCuration	2023-03-17
MONDO:0013755	PYCR1-related de Barsy syndrome	skos:exactMatch	DOID:0070138	autosomal recessive cutis laxa type IIIB	semapv:ManualMappingCuration	2023-03-17
MONDO:0013758	Charcot-Marie-Tooth disease dominant intermediate E	skos:exactMatch	DOID:0110205	Charcot-Marie-Tooth disease dominant intermediate E	semapv:ManualMappingCuration	2023-03-17
MONDO:0013766	familial cold autoinflammatory syndrome 3	skos:exactMatch	DOID:0090064	familial cold autoinflammatory syndrome 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0013767	autoimmune lymphoproliferative syndrome type 4	skos:exactMatch	DOID:0110117	autoimmune lymphoproliferative syndrome type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0013770	atrial septal defect 9	skos:exactMatch	DOID:0110114	atrial heart septal defect 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0013775	thrombomodulin-related bleeding disorder	skos:exactMatch	DOID:0111908	thrombophilia due to thrombomodulin defect	semapv:ManualMappingCuration	2023-04-17
MONDO:0013776	spastic ataxia 5	skos:exactMatch	DOID:0050944	spastic ataxia 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0013788	Usher syndrome type 3B	skos:exactMatch	DOID:0110842	Usher syndrome type 3B	semapv:ManualMappingCuration	2024-04-21
MONDO:0013789	DDOST-congenital disorder of glycosylation	skos:exactMatch	DOID:0080569	congenital disorder of glycosylation Ir	semapv:ManualMappingCuration	2023-03-17
MONDO:0013795	fibrochondrogenesis 2	skos:exactMatch	DOID:0080673	fibrochondrogenesis 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0013796	chromosome 17q12 duplication syndrome	skos:exactMatch	DOID:0060433	chromosome 17q12 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013797	chromosome 17q12 deletion syndrome	skos:exactMatch	DOID:0060404	chromosome 17q12 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013801	developmental and epileptic encephalopathy, 13	skos:exactMatch	DOID:0080445	developmental and epileptic encephalopathy 13	semapv:ManualMappingCuration	2024-04-21
MONDO:0013802	infantile cerebellar-retinal degeneration	skos:exactMatch	DOID:0050883	infantile cerebellar-retinal degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0013805	intellectual disability, autosomal dominant 13	skos:exactMatch	DOID:0070043	autosomal dominant intellectual developmental disorder 13	semapv:ManualMappingCuration	2023-04-17
MONDO:0013808	Maffucci syndrome	skos:exactMatch	DOID:0060221	Maffucci syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013810	COG6-ongenital disorder of glycosylation	skos:exactMatch	DOID:0070264	congenital disorder of glycosylation type IIl	semapv:ManualMappingCuration	2023-03-17
MONDO:0013811	combined oxidative phosphorylation defect type 9	skos:exactMatch	DOID:0111472	combined oxidative phosphorylation deficiency 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0013813	dystonia 21	skos:exactMatch	DOID:0090046	dystonia 21	semapv:ManualMappingCuration	2023-03-17
MONDO:0013819	intellectual disability, autosomal dominant 14	skos:exactMatch	DOID:0070044	Coffin-Siris syndrome 2	semapv:ManualMappingCuration	2024-08-18
MONDO:0013821	intellectual disability, autosomal dominant 16	skos:exactMatch	DOID:0070046	Coffin-Siris syndrome 4	semapv:ManualMappingCuration	2024-08-18
MONDO:0013824	Joubert syndrome 17	skos:exactMatch	DOID:0110986	Joubert Syndrome 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0013825	congenital diarrhea 6	skos:exactMatch	DOID:0060780	congenital diarrhea 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0013826	autosomal recessive nonsyndromic hearing loss 86	skos:exactMatch	DOID:0110532	autosomal recessive nonsyndromic deafness 86	semapv:ManualMappingCuration	2024-04-21
MONDO:0013835	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7	skos:exactMatch	DOID:0111234	congenital muscular dystrophy-dystroglycanopathy A7	semapv:ManualMappingCuration	2023-03-17
MONDO:0013836	familial steroid-resistant nephrotic syndrome with sensorineural deafness	skos:exactMatch	DOID:0070243	primary coenzyme Q10 deficiency 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0013837	deafness-encephaloneuropathy-obesity-valvulopathy syndrome	skos:exactMatch	DOID:0070239	primary coenzyme Q10 deficiency 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0013838	coenzyme Q10 deficiency, primary, 3	skos:exactMatch	DOID:0070240	primary coenzyme Q10 deficiency 3	semapv:ManualMappingCuration	2024-02-18
MONDO:0013839	hereditary sensory and autonomic neuropathy type 6	skos:exactMatch	DOID:0070151	hereditary sensory and autonomic neuropathy type 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0013840	encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome	skos:exactMatch	DOID:0070242	primary coenzyme Q10 deficiency 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0013847	chromosome 16p11.2 duplication syndrome	skos:exactMatch	DOID:0060430	chromosome 16p11.2 duplication syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013848	dilated cardiomyopathy 2B	skos:exactMatch	DOID:0110441	dilated cardiomyopathy 2B	semapv:ManualMappingCuration	2024-02-18
MONDO:0013859	cataract 38	skos:exactMatch	DOID:0110245	cataract 38	semapv:ManualMappingCuration	2024-04-21
MONDO:0013862	immunodeficiency, common variable, 7	skos:exactMatch	DOID:0081150	common variable immunodeficiency 7	semapv:ManualMappingCuration	2023-06-18
MONDO:0013863	combined immunodeficiency due to LRBA deficiency	skos:exactMatch	DOID:0081151	common variable immunodeficiency 8	semapv:ManualMappingCuration	2023-06-18
MONDO:0013865	mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency	skos:exactMatch	DOID:0111480	combined oxidative phosphorylation deficiency 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0013866	neuronal ceroid lipofuscinosis 11	skos:exactMatch	DOID:0110732	neuronal ceroid lipofuscinosis 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0013869	adenine phosphoribosyltransferase deficiency	skos:exactMatch	DOID:0060350	adenine phosphoribosyltransferase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013870	TMEM165-congenital disorder of glycosylation	skos:exactMatch	DOID:0070263	congenital disorder of glycosylation type IIk	semapv:ManualMappingCuration	2023-03-17
MONDO:0013873	IMAGe syndrome	skos:exactMatch	DOID:0050885	IMAGe syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013875	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome	skos:exactMatch	DOID:0110001	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0013877	mitochondrial pyruvate carrier deficiency	skos:exactMatch	DOID:0080363	mitochondrial pyruvate carrier deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013884	neuronopathy, distal hereditary motor, type 5B	skos:exactMatch	DOID:0111205	autosomal dominant distal hereditary motor neuronopathy 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0013885	Malan overgrowth syndrome	skos:exactMatch	DOID:0112102	Sotos syndrome 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0013886	cerebellar dysfunction with variable cognitive and behavioral abnormalities	skos:exactMatch	DOID:0050998	nonprogressive cerebellar ataxia with mental retardation	semapv:ManualMappingCuration	2023-03-17
MONDO:0013890	congenital myopathy with internal nuclei and atypical cores	skos:exactMatch	DOID:0111224	centronuclear myopathy 4	semapv:ManualMappingCuration	2023-04-17
MONDO:0013891	amyotrophic lateral sclerosis type 18	skos:exactMatch	DOID:0060209	amyotrophic lateral sclerosis type 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0013896	Joubert syndrome 18	skos:exactMatch	DOID:0110987	Joubert Syndrome 18	semapv:ManualMappingCuration	2024-04-21
MONDO:0013898	karyomegalic interstitial nephritis	skos:exactMatch	DOID:0060911	karyomegalic interstitial nephritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0013901	spermatogenic failure 10	skos:exactMatch	DOID:0070178	spermatogenic failure 10	semapv:ManualMappingCuration	2024-02-18
MONDO:0013904	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8	skos:exactMatch	DOID:0111231	congenital muscular dystrophy-dystroglycanopathy type A8	semapv:ManualMappingCuration	2023-03-17
MONDO:0013905	autosomal recessive spinocerebellar ataxia 13	skos:exactMatch	DOID:0080062	autosomal recessive spinocerebellar ataxia 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0013906	amelogenesis imperfecta hypomaturation type 2A4	skos:exactMatch	DOID:0110062	amelogenesis imperfecta hypomaturation type 2A4	semapv:ManualMappingCuration	2023-03-17
MONDO:0013907	bilateral generalized polymicrogyria	skos:exactMatch	DOID:0080920	bilateral generalized polymicrogyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0013922	Seckel syndrome 7	skos:exactMatch	DOID:0070011	Seckel syndrome 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0013927	peroxisome biogenesis disorder 3A (Zellweger)	skos:exactMatch	DOID:0080478	peroxisome biogenesis disorder 3A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013928	dystonia 23	skos:exactMatch	DOID:0090051	dystonia 23	semapv:ManualMappingCuration	2023-03-17
MONDO:0013930	peroxisome biogenesis disorder 4A (Zellweger)	skos:exactMatch	DOID:0080479	peroxisome biogenesis disorder 4A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013931	peroxisome biogenesis disorder 4B	skos:exactMatch	DOID:0081433	Peroxisome biogenesis disorder 4B	semapv:ManualMappingCuration	2024-05-19
MONDO:0013932	peroxisome biogenesis disorder 5A (Zellweger)	skos:exactMatch	DOID:0080480	peroxisome biogenesis disorder 5A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013936	peroxisome biogenesis disorder 6A (Zellweger)	skos:exactMatch	DOID:0080481	peroxisome biogenesis disorder 6A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013937	peroxisome biogenesis disorder 6B	skos:exactMatch	DOID:0081435	Peroxisome biogenesis disorder 6B	semapv:ManualMappingCuration	2024-05-19
MONDO:0013938	peroxisome biogenesis disorder 7A (Zellweger)	skos:exactMatch	DOID:0080482	peroxisome biogenesis disorder 7A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013942	peroxisome biogenesis disorder 8A (Zellweger)	skos:exactMatch	DOID:0080483	peroxisome biogenesis disorder 8A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013947	neuronopathy, distal hereditary motor, autosomal recessive 5	skos:exactMatch	DOID:0111214	autosomal recessive distal hereditary motor neuronopathy 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0013948	peroxisome biogenesis disorder 10A (Zellweger)	skos:exactMatch	DOID:0080484	peroxisome biogenesis disorder 10A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013949	peroxisome biogenesis disorder 11A (Zellweger)	skos:exactMatch	DOID:0080485	peroxisome biogenesis disorder 11A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013950	peroxisome biogenesis disorder 11B	skos:exactMatch	DOID:0081439	Peroxisome biogenesis disorder 11B	semapv:ManualMappingCuration	2024-05-19
MONDO:0013951	peroxisome biogenesis disorder 12A (Zellweger)	skos:exactMatch	DOID:0080486	peroxisome biogenesis disorder 12A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013952	peroxisome biogenesis disorder 13A (Zellweger)	skos:exactMatch	DOID:0080487	peroxisome biogenesis disorder 13A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013953	immunodeficiency 28	skos:exactMatch	DOID:0111995	immunodeficiency 28	semapv:ManualMappingCuration	2024-04-21
MONDO:0013954	Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency	skos:exactMatch	DOID:0111950	immunodeficiency 29	semapv:ManualMappingCuration	2023-04-17
MONDO:0013955	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency	skos:exactMatch	DOID:0111990	immunodeficiency 30	semapv:ManualMappingCuration	2023-04-17
MONDO:0013956	Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency	skos:exactMatch	DOID:0111945	immunodeficiency 31A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013957	Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency	skos:exactMatch	DOID:0111986	immunodeficiency 32A	semapv:ManualMappingCuration	2023-04-17
MONDO:0013959	Charcot-Marie-Tooth disease type 4F	skos:exactMatch	DOID:0110193	Charcot-Marie-Tooth disease type 4F	semapv:ManualMappingCuration	2023-03-17
MONDO:0013962	hereditary spastic paraplegia 53	skos:exactMatch	DOID:0110805	hereditary spastic paraplegia 53	semapv:ManualMappingCuration	2023-03-17
MONDO:0013966	catecholaminergic polymorphic ventricular tachycardia 4	skos:exactMatch	DOID:0060678	catecholaminergic polymorphic ventricular tachycardia 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0013967	peroxisome biogenesis disorder 14B	skos:exactMatch	DOID:0081274	peroxisome biogenesis disorder 14B	semapv:ManualMappingCuration	2023-04-17
MONDO:0013968	PGM1-congenital disorder of glycosylation	skos:exactMatch	DOID:0080570	congenital disorder of glycosylation It	semapv:ManualMappingCuration	2023-03-17
MONDO:0013969	combined oxidative phosphorylation defect type 11	skos:exactMatch	DOID:0111481	combined oxidative phosphorylation deficiency 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0013970	branched-chain keto acid dehydrogenase kinase deficiency	skos:exactMatch	DOID:0090126	branched-chain keto acid dehydrogenase kinase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013971	leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome	skos:exactMatch	DOID:0111493	combined oxidative phosphorylation deficiency 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0013975	ectodermal dysplasia 7, hair/nail type	skos:exactMatch	DOID:0111660	ectodermal dysplasia 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0013977	combined oxidative phosphorylation defect type 13	skos:exactMatch	DOID:0111467	combined oxidative phosphorylation deficiency 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0013978	autosomal recessive nonsyndromic hearing loss 70	skos:exactMatch	DOID:0110521	autosomal recessive nonsyndromic deafness 70	semapv:ManualMappingCuration	2024-04-21
MONDO:0013986	combined oxidative phosphorylation defect type 14	skos:exactMatch	DOID:0111477	combined oxidative phosphorylation deficiency 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0013987	combined oxidative phosphorylation defect type 15	skos:exactMatch	DOID:0111491	combined oxidative phosphorylation deficiency 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0013989	developmental and epileptic encephalopathy, 14	skos:exactMatch	DOID:0080439	developmental and epileptic encephalopathy 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0013990	pontocerebellar hypoplasia type 8	skos:exactMatch	DOID:0060277	pontocerebellar hypoplasia type 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0013991	obesity due to congenital leptin deficiency	skos:exactMatch	DOID:0111334	congenital leptin deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0013993	pontocerebellar hypoplasia type 7	skos:exactMatch	DOID:0060276	pontocerebellar hypoplasia type 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0014002	autosomal dominant nocturnal frontal lobe epilepsy 5	skos:exactMatch	DOID:0060686	autosomal dominant nocturnal frontal lobe epilepsy 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0014006	Schuurs-Hoeijmakers syndrome	skos:exactMatch	DOID:0070047	Schuurs-Hoeijmakers syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014012	Charcot-Marie-Tooth disease axonal type 2Q	skos:exactMatch	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q	semapv:ManualMappingCuration	2023-03-17
MONDO:0014015	hereditary spastic paraplegia 56	skos:exactMatch	DOID:0110808	hereditary spastic paraplegia 56	semapv:ManualMappingCuration	2023-03-17
MONDO:0014016	hereditary spastic paraplegia 49	skos:exactMatch	DOID:0110801	hereditary spastic paraplegia 49	semapv:ManualMappingCuration	2023-03-17
MONDO:0014018	hereditary spastic paraplegia 54	skos:exactMatch	DOID:0110806	hereditary spastic paraplegia 54	semapv:ManualMappingCuration	2023-03-17
MONDO:0014020	hereditary spastic paraplegia 55	skos:exactMatch	DOID:0110807	hereditary spastic paraplegia 55	semapv:ManualMappingCuration	2023-03-17
MONDO:0014021	familial episodic pain syndrome with predominantly upper body involvement	skos:exactMatch	DOID:0111729	familial episodic pain syndrome 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0014022	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10	skos:exactMatch	DOID:0111239	congenital muscular dystrophy-dystroglycanopathy type A10	semapv:ManualMappingCuration	2023-03-17
MONDO:0014023	congenital muscular dystrophy with intellectual disability and severe epilepsy	skos:exactMatch	DOID:0080571	congenital disorder of glycosylation Iu	semapv:ManualMappingCuration	2023-03-17
MONDO:0014024	hereditary spastic paraplegia 43	skos:exactMatch	DOID:0110795	hereditary spastic paraplegia 43	semapv:ManualMappingCuration	2023-03-17
MONDO:0014025	lower motor neuron syndrome with late-adult onset	skos:exactMatch	DOID:0081356	spinal muscular atrophy, Jokela type	semapv:ManualMappingCuration	2023-07-09
MONDO:0014028	distal arthrogryposis type 5D	skos:exactMatch	DOID:0111594	distal arthrogryposis type 5D	semapv:ManualMappingCuration	2023-03-17
MONDO:0014033	dystonia 25	skos:exactMatch	DOID:0090055	dystonia 25	semapv:ManualMappingCuration	2023-03-17
MONDO:0014034	severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome	skos:exactMatch	DOID:0070048	GAND syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014035	severe intellectual disability-progressive spastic diplegia syndrome	skos:exactMatch	DOID:0070049	autosomal dominant intellectual developmental disorder 19	semapv:ManualMappingCuration	2023-03-17
MONDO:0014037	spermatogenic failure 11	skos:exactMatch	DOID:0070180	spermatogenic failure 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0014039	mitochondrial DNA depletion syndrome 11	skos:exactMatch	DOID:0080129	mitochondrial DNA depletion syndrome 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0014043	microcephalic primordial dwarfism due to ZNF335 deficiency	skos:exactMatch	DOID:0070294	primary autosomal recessive microcephaly 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0014047	Cowden syndrome 5	skos:exactMatch	DOID:0081001	Cowden syndrome 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0014048	Cowden syndrome 6	skos:exactMatch	DOID:0081002	Cowden syndrome 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0014052	congenital myasthenic syndrome 8	skos:exactMatch	DOID:0110657	congenital myasthenic syndrome 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0014062	mitochondrial DNA deletion syndrome with progressive myopathy	skos:exactMatch	DOID:0111519	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0014067	short ulna-dysmorphism-hypotonia-intellectual disability syndrome	skos:exactMatch	DOID:0081201	autosomal recessive intellectual developmental disorder 35	semapv:ManualMappingCuration	2023-06-18
MONDO:0014070	oculocutaneous albinism type 7	skos:exactMatch	DOID:0070100	oculocutaneous albinism type VII	semapv:ManualMappingCuration	2023-03-17
MONDO:0014071	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11	skos:exactMatch	DOID:0111230	congenital muscular dystrophy-dystroglycanopathy type A11	semapv:ManualMappingCuration	2023-03-17
MONDO:0014072	D,L-2-hydroxyglutaric aciduria	skos:exactMatch	DOID:0111619	combined D-2- and L-2-hydroxyglutaric aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0014073	dilated cardiomyopathy 1II	skos:exactMatch	DOID:0110450	dilated cardiomyopathy 1II	semapv:ManualMappingCuration	2024-02-18
MONDO:0014074	Charcot-Marie-Tooth disease dominant intermediate F	skos:exactMatch	DOID:0110206	Charcot-Marie-Tooth disease dominant intermediate F	semapv:ManualMappingCuration	2023-03-17
MONDO:0014076	dyskeratosis congenita, autosomal recessive 5	skos:exactMatch	DOID:0070022	autosomal recessive dyskeratosis congenita 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0014077	cobblestone lissencephaly without muscular or ocular involvement	skos:exactMatch	DOID:0112230	lissencephaly 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0014078	platelet-type bleeding disorder 15	skos:exactMatch	DOID:0111053	platelet-type bleeding disorder 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0014080	osteosclerotic metaphyseal dysplasia	skos:exactMatch	DOID:0081111	osteosclerotic metaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0014081	severe combined immunodeficiency due to CARD11 deficiency	skos:exactMatch	DOID:0111957	immunodeficiency 11A	semapv:ManualMappingCuration	2023-04-17
MONDO:0014082	cryptosporidiosis-chronic cholangitis-liver disease syndrome	skos:exactMatch	DOID:0111982	immunodeficiency 56	semapv:ManualMappingCuration	2023-06-18
MONDO:0014083	agammaglobulinemia 7, autosomal recessive	skos:exactMatch	DOID:0081139	agammaglobulinemia 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0014091	mitochondrial complex V (ATP synthase) deficiency nuclear type 4B	skos:exactMatch	DOID:0070462	mitochondrial complex V (ATP synthase) deficiency nuclear type 4B	semapv:ManualMappingCuration	2024-04-21
MONDO:0014095	dilated cardiomyopathy 1JJ	skos:exactMatch	DOID:0110438	dilated cardiomyopathy 1JJ	semapv:ManualMappingCuration	2024-02-18
MONDO:0014098	CIDEC-related familial partial lipodystrophy	skos:exactMatch	DOID:0070203	familial partial lipodystrophy type 5	semapv:ManualMappingCuration	2023-11-19
MONDO:0014100	dilated cardiomyopathy 1KK	skos:exactMatch	DOID:0110445	dilated cardiomyopathy 1KK	semapv:ManualMappingCuration	2024-02-18
MONDO:0014101	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12	skos:exactMatch	DOID:0111235	congenital muscular dystrophy-dystroglycanopathy type A12	semapv:ManualMappingCuration	2023-03-17
MONDO:0014108	Fanconi anemia complementation group Q	skos:exactMatch	DOID:0111093	Fanconi anemia complementation group Q	semapv:ManualMappingCuration	2024-04-21
MONDO:0014117	Charcot-Marie-Tooth disease type 4B3	skos:exactMatch	DOID:0110194	Charcot-Marie-Tooth disease type 4B3	semapv:ManualMappingCuration	2023-03-17
MONDO:0014118	congenital neutropenia-myelofibrosis-nephromegaly syndrome	skos:exactMatch	DOID:0112132	severe congenital neutropenia 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0014119	intellectual disability-strabismus syndrome	skos:exactMatch	DOID:0081099	neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies	semapv:ManualMappingCuration	2023-04-17
MONDO:0014120	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13	skos:exactMatch	DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13	semapv:ManualMappingCuration	2023-03-17
MONDO:0014121	autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures	skos:exactMatch	DOID:0070349	spinal muscular atrophy with lower extremity predominant 2A	semapv:ManualMappingCuration	2023-06-18
MONDO:0014125	symphalangism, proximal, 1B	skos:exactMatch	DOID:0080788	proximal symphalangism 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0014127	oculocutaneous albinism type 5	skos:exactMatch	DOID:0070099	oculocutaneous albinism type V	semapv:ManualMappingCuration	2023-03-17
MONDO:0014132	multiple mitochondrial dysfunctions syndrome 3	skos:exactMatch	DOID:0080135	multiple mitochondrial dysfunctions syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0014137	precocious puberty, central, 2	skos:exactMatch	DOID:0112309	central precocious puberty 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0014138	nemaline myopathy 8	skos:exactMatch	DOID:0110930	nemaline myopathy 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0014140	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14	skos:exactMatch	DOID:0111233	congenital muscular dystrophy-dystroglycanopathy A14	semapv:ManualMappingCuration	2023-03-17
MONDO:0014141	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14	skos:exactMatch	DOID:0112377	muscular dystrophy-dystroglycanopathy type B14	semapv:ManualMappingCuration	2023-06-18
MONDO:0014142	autosomal recessive limb-girdle muscular dystrophy type 2T	skos:exactMatch	DOID:0110294	autosomal recessive limb-girdle muscular dystrophy type 2T	semapv:ManualMappingCuration	2023-03-17
MONDO:0014144	autosomal recessive limb-girdle muscular dystrophy type R18	skos:exactMatch	DOID:0110287	autosomal recessive limb-girdle muscular dystrophy type 2S	semapv:ManualMappingCuration	2023-03-17
MONDO:0014145	Leber congenital amaurosis 17	skos:exactMatch	DOID:0110217	Leber congenital amaurosis 17	semapv:ManualMappingCuration	2024-04-21
MONDO:0014147	neuronal ceroid lipofuscinosis 13	skos:exactMatch	DOID:0110727	neuronal ceroid lipofuscinosis 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0014154	Charcot-Marie-Tooth disease recessive intermediate C	skos:exactMatch	DOID:0110198	Charcot-Marie-Tooth disease recessive intermediate C	semapv:ManualMappingCuration	2023-03-17
MONDO:0014158	nephronophthisis 16	skos:exactMatch	DOID:0111124	nephronophthisis 16	semapv:ManualMappingCuration	2023-03-17
MONDO:0014159	autosomal recessive spinocerebellar ataxia 14	skos:exactMatch	DOID:0080058	autosomal recessive spinocerebellar ataxia 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0014160	TCR-alpha-beta-positive T-cell deficiency	skos:exactMatch	DOID:0111977	immunodeficiency 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0014162	infantile hypertrophic cardiomyopathy due to MRPL44 deficiency	skos:exactMatch	DOID:0111469	combined oxidative phosphorylation deficiency 16	semapv:ManualMappingCuration	2023-03-17
MONDO:0014165	multiple congenital anomalies-hypotonia-seizures syndrome 3	skos:exactMatch	DOID:0080140	multiple congenital anomalies-hypotonia-seizures syndrome 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0014168	severe combined immunodeficiency due to CORO1A deficiency	skos:exactMatch	DOID:0060019	coronin-1A deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0014175	mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive	skos:exactMatch	DOID:0080335	mitochondrial DNA depletion syndrome 12b	semapv:ManualMappingCuration	2023-03-17
MONDO:0014185	chromosome 3q13.31 deletion syndrome	skos:exactMatch	DOID:0060418	chromosome 3q13.31 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014189	age related macular degeneration 13	skos:exactMatch	DOID:0110025	age related macular degeneration 13	semapv:ManualMappingCuration	2024-04-21
MONDO:0014190	combined oxidative phosphorylation defect type 17	skos:exactMatch	DOID:0111496	combined oxidative phosphorylation deficiency 17	semapv:ManualMappingCuration	2023-03-17
MONDO:0014197	combined immunodeficiency due to MALT1 deficiency	skos:exactMatch	DOID:0111988	immunodeficiency 12	semapv:ManualMappingCuration	2023-04-17
MONDO:0014198	mitochondrial DNA depletion syndrome 13	skos:exactMatch	DOID:0080131	mitochondrial DNA depletion syndrome 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0014201	developmental and epileptic encephalopathy, 18	skos:exactMatch	DOID:0080413	developmental and epileptic encephalopathy 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0014205	severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome	skos:exactMatch	DOID:0080893	Bainbridge-Ropers syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0014208	Charcot-Marie-Tooth disease type 2R	skos:exactMatch	DOID:0110161	Charcot-Marie-Tooth disease type 2R	semapv:ManualMappingCuration	2023-03-17
MONDO:0014209	early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome	skos:exactMatch	DOID:0112344	hereditary spastic paraplegia 79B	semapv:ManualMappingCuration	2023-04-17
MONDO:0014210	intellectual disability-hypotonia-spasticity-sleep disorder syndrome	skos:exactMatch	DOID:0081202	autosomal recessive intellectual developmental disorder 37	semapv:ManualMappingCuration	2023-06-18
MONDO:0014212	sulfite oxidase deficiency due to molybdenum cofactor deficiency type C	skos:exactMatch	DOID:0111166	molybdenum cofactor deficiency type C	semapv:ManualMappingCuration	2023-03-17
MONDO:0014213	intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome	skos:exactMatch	DOID:0070051	autosomal dominant intellectual developmental disorder 21	semapv:ManualMappingCuration	2023-03-17
MONDO:0014221	triosephosphate isomerase deficiency	skos:exactMatch	DOID:0050884	triosephosphate isomerase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0014224	developmental delay with autism spectrum disorder and gait instability	skos:exactMatch	DOID:0081203	autosomal recessive intellectual developmental disorder 38	semapv:ManualMappingCuration	2023-06-18
MONDO:0014225	hemochromatosis type 5	skos:exactMatch	DOID:0111031	hemochromatosis type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0014226	idiopathic CD4 lymphocytopenia	skos:exactMatch	DOID:0111987	immunodeficiency 13	semapv:ManualMappingCuration	2023-04-17
MONDO:0014234	reticulate acropigmentation of Kitamura	skos:exactMatch	DOID:0060258	reticulate acropigmentation of Kitamura	semapv:ManualMappingCuration	2023-03-17
MONDO:0014238	severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome	skos:exactMatch	DOID:0081204	autosomal recessive intellectual developmental disorder 39	semapv:ManualMappingCuration	2023-06-18
MONDO:0014242	van Maldergem syndrome 2	skos:exactMatch	DOID:0080586	Van Maldergem syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0014243	Schaaf-Yang syndrome	skos:exactMatch	DOID:0111715	Schaaf-Yang syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014244	hereditary sensory and autonomic neuropathy type 7	skos:exactMatch	DOID:0070149	hereditary sensory and autonomic neuropathy type 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0014246	episodic pain syndrome, familial, 2	skos:exactMatch	DOID:0111730	familial episodic pain syndrome 2	semapv:ManualMappingCuration	2024-02-18
MONDO:0014247	familial episodic pain syndrome with predominantly lower limb involvement	skos:exactMatch	DOID:0111731	familial episodic pain syndrome 3	semapv:ManualMappingCuration	2023-06-18
MONDO:0014252	familial hypobetalipoproteinemia 1	skos:exactMatch	DOID:0111062	familial hypobetalipoproteinemia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0014260	immunodeficiency, common variable, 10	skos:exactMatch	DOID:0081152	common variable immunodeficiency 10	semapv:ManualMappingCuration	2023-06-18
MONDO:0014261	growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome	skos:exactMatch	DOID:0111484	combined oxidative phosphorylation deficiency 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0014265	Alzheimer disease 18	skos:exactMatch	DOID:0110050	Alzheimer's disease 18	semapv:ManualMappingCuration	2024-04-21
MONDO:0014267	severe combined immunodeficiency due to IKK2 deficiency	skos:exactMatch	DOID:0111959	immunodeficiency 15B	semapv:ManualMappingCuration	2023-04-17
MONDO:0014268	combined immunodeficiency due to OX40 deficiency	skos:exactMatch	DOID:0111935	immunodeficiency 16	semapv:ManualMappingCuration	2023-04-17
MONDO:0014269	combined oxidative phosphorylation deficiency 19	skos:exactMatch	DOID:0111476	combined oxidative phosphorylation deficiency 19	semapv:ManualMappingCuration	2024-02-18
MONDO:0014270	STT3A-congenital disorder of glycosylation	skos:exactMatch	DOID:0080572	congenital disorder of glycosylation Iw	semapv:ManualMappingCuration	2023-03-17
MONDO:0014271	STT3B-congenital disorder of glycosylation	skos:exactMatch	DOID:0080573	congenital disorder of glycosylation Ix	semapv:ManualMappingCuration	2023-03-17
MONDO:0014273	microcephaly-thin corpus callosum-intellectual disability syndrome	skos:exactMatch	DOID:0081205	autosomal recessive intellectual developmental disorder 40	semapv:ManualMappingCuration	2023-06-18
MONDO:0014276	combined immunodeficiency due to CD3gamma deficiency	skos:exactMatch	DOID:0060018	CD3gamma deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0014276	combined immunodeficiency due to CD3gamma deficiency	skos:exactMatch	DOID:0111973	immunodeficiency 17	semapv:ManualMappingCuration	2023-04-17
MONDO:0014278	immunodeficiency 18	skos:exactMatch	DOID:0060017	CD3epsilon deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0014278	immunodeficiency 18	skos:exactMatch	DOID:0111971	immunodeficiency 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0014280	immunodeficiency 19	skos:exactMatch	DOID:0060016	CD3delta deficiency	semapv:ManualMappingCuration	2024-02-18
MONDO:0014280	immunodeficiency 19	skos:exactMatch	DOID:0111972	immunodeficiency 19	semapv:ManualMappingCuration	2024-02-18
MONDO:0014282	hereditary spastic paraplegia 72	skos:exactMatch	DOID:0110817	hereditary spastic paraplegia 72A	semapv:ManualMappingCuration	2023-03-17
MONDO:0014284	short-rib thoracic dysplasia 10 with or without polydactyly	skos:exactMatch	DOID:0110091	short-rib thoracic dysplasia 10 with or without polydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0014286	neuropathy, hereditary sensory, type 1F	skos:exactMatch	DOID:0070154	hereditary sensory neuropathy type 1F	semapv:ManualMappingCuration	2023-03-17
MONDO:0014289	macrocephaly-developmental delay syndrome	skos:exactMatch	DOID:0081206	autosomal recessive intellectual developmental disorder 41	semapv:ManualMappingCuration	2023-06-18
MONDO:0014290	neurodegeneration with brain iron accumulation 6	skos:exactMatch	DOID:0110740	neurodegeneration with brain iron accumulation 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0014294	chromosome 15q11.2 deletion syndrome	skos:exactMatch	DOID:0060393	chromosome 15q11.2 deletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014295	hereditary spastic paraplegia 57	skos:exactMatch	DOID:0110809	hereditary spastic paraplegia 57	semapv:ManualMappingCuration	2024-04-21
MONDO:0014300	proximal myopathy with extrapyramidal signs	skos:exactMatch	DOID:0111335	myopathy with extrapyramidal signs	semapv:ManualMappingCuration	2023-03-17
MONDO:0014302	hereditary spastic paraplegia 62	skos:exactMatch	DOID:0110813	hereditary spastic paraplegia 62	semapv:ManualMappingCuration	2023-03-17
MONDO:0014303	hereditary spastic paraplegia 64	skos:exactMatch	DOID:0110815	hereditary spastic paraplegia 64	semapv:ManualMappingCuration	2023-03-17
MONDO:0014304	hereditary spastic paraplegia 61	skos:exactMatch	DOID:0110812	hereditary spastic paraplegia 61	semapv:ManualMappingCuration	2023-03-17
MONDO:0014305	hereditary spastic paraplegia 63	skos:exactMatch	DOID:0110814	hereditary spastic paraplegia 63	semapv:ManualMappingCuration	2023-03-17
MONDO:0014311	autosomal recessive spinocerebellar ataxia 15	skos:exactMatch	DOID:0080057	autosomal recessive spinocerebellar ataxia 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0014313	autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity	skos:exactMatch	DOID:0111941	immunodeficiency 20	semapv:ManualMappingCuration	2023-04-17
MONDO:0014320	Bosch-Boonstra-Schaaf optic atrophy syndrome	skos:exactMatch	DOID:0112226	Bosch-Boonstra-Schaaf optic atrophy syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014326	nemaline myopathy 9	skos:exactMatch	DOID:0110929	nemaline myopathy 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0014327	palmoplantar keratoderma, nonepidermolytic, focal or diffuse	skos:exactMatch	DOID:0111710	focal or diffuse nonepidermolytic palmoplantar keratoderma	semapv:ManualMappingCuration	2023-04-17
MONDO:0014328	developmental and epileptic encephalopathy, 19	skos:exactMatch	DOID:0080431	developmental and epileptic encephalopathy 19	semapv:ManualMappingCuration	2024-02-18
MONDO:0014334	severe combined immunodeficiency due to LCK deficiency	skos:exactMatch	DOID:0111937	immunodeficiency 22	semapv:ManualMappingCuration	2023-04-17
MONDO:0014336	intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency	skos:exactMatch	DOID:0070053	autosomal dominant intellectual developmental disorder 23	semapv:ManualMappingCuration	2023-03-17
MONDO:0014337	complex cortical dysplasia with other brain malformations 5	skos:exactMatch	DOID:0090135	complex cortical dysplasia with other brain malformations 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0014339	autosomal recessive spinocerebellar ataxia 16	skos:exactMatch	DOID:0080029	autosomal recessive spinocerebellar ataxia 16	semapv:ManualMappingCuration	2023-03-17
MONDO:0014341	complex cortical dysplasia with other brain malformations 6	skos:exactMatch	DOID:0090136	complex cortical dysplasia with other brain malformations 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0014349	pontocerebellar hypoplasia type 10	skos:exactMatch	DOID:0060279	pontocerebellar hypoplasia type 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0014350	Seckel syndrome 8	skos:exactMatch	DOID:0070009	Seckel syndrome 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0014351	pontocerebellar hypoplasia type 9	skos:exactMatch	DOID:0060278	pontocerebellar hypoplasia type 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0014353	immunodeficiency 23	skos:exactMatch	DOID:0111953	immunodeficiency 23	semapv:ManualMappingCuration	2023-03-17
MONDO:0014357	intellectual disability, autosomal dominant 24	skos:exactMatch	DOID:0070054	Vulto-van Silfout-de Vries syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0014361	autism spectrum disorder due to AUTS2 deficiency	skos:exactMatch	DOID:0070056	autosomal dominant intellectual developmental disorder 26	semapv:ManualMappingCuration	2023-03-17
MONDO:0014365	spermatogenic failure 13	skos:exactMatch	DOID:0070182	spermatogenic failure 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0014366	spermatogenic failure 14	skos:exactMatch	DOID:0070179	spermatogenic failure 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0014369	postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome	skos:exactMatch	DOID:0080328	Culler-Jones syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014370	pontocerebellar hypoplasia type 2E	skos:exactMatch	DOID:0060271	pontocerebellar hypoplasia type 2E	semapv:ManualMappingCuration	2024-02-18
MONDO:0014375	congenital diarrhea 7 with exudative enteropathy	skos:exactMatch	DOID:0060778	congenital diarrhea 7 with exudative enteropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0014379	ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder	skos:exactMatch	DOID:0070058	Helsmoortel-Van Der Aa syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014380	colobomatous microphthalmia-rhizomelic dysplasia syndrome	skos:exactMatch	DOID:0111802	syndromic microphthalmia 14	semapv:ManualMappingCuration	2023-11-19
MONDO:0014382	Tatton-Brown-Rahman overgrowth syndrome	skos:exactMatch	DOID:0112339	Tatton-Brown-Rahman syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0014383	myopathy, tubular aggregate, 2	skos:exactMatch	DOID:0080686	tubular aggregate myopathy 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0014386	platelet-type bleeding disorder 18	skos:exactMatch	DOID:0111051	platelet-type bleeding disorder 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0014387	leukoencephalopathy, progressive, with ovarian failure	skos:exactMatch	DOID:0070396	progressive leukoencephalopathy with ovarian failure	semapv:ManualMappingCuration	2024-04-21
MONDO:0014388	familial median cleft of the upper and lower lips	skos:exactMatch	DOID:0080407	orofacial cleft 14	semapv:ManualMappingCuration	2023-06-18
MONDO:0014391	severe combined immunodeficiency due to CTPS1 deficiency	skos:exactMatch	DOID:0111938	immunodeficiency 24	semapv:ManualMappingCuration	2023-04-17
MONDO:0014397	combined oxidative phosphorylation defect type 20	skos:exactMatch	DOID:0111478	combined oxidative phosphorylation deficiency 20	semapv:ManualMappingCuration	2023-03-17
MONDO:0014401	tall stature-scoliosis-macrodactyly of the great toes syndrome	skos:exactMatch	DOID:0070316	Miura type epiphyseal chondrodysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0014405	STING-associated vasculopathy with onset in infancy	skos:exactMatch	DOID:0111457	STING-associated vasculopathy with onset in infancy	semapv:ManualMappingCuration	2023-03-17
MONDO:0014410	spinocerebellar ataxia type 37	skos:exactMatch	DOID:0050984	spinocerebellar ataxia type 37	semapv:ManualMappingCuration	2023-03-17
MONDO:0014413	orofaciodigital syndrome type 14	skos:exactMatch	DOID:0060958	orofaciodigital syndrome XIV	semapv:ManualMappingCuration	2024-07-21
MONDO:0014418	myopathy, centronuclear, 5	skos:exactMatch	DOID:0111222	centronuclear myopathy 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0014423	severe combined immunodeficiency due to DNA-PKcs deficiency	skos:exactMatch	DOID:0111961	immunodeficiency 26	semapv:ManualMappingCuration	2023-04-17
MONDO:0014428	autosomal recessive nonsyndromic hearing loss 102	skos:exactMatch	DOID:0110463	autosomal recessive nonsyndromic deafness 102	semapv:ManualMappingCuration	2023-03-17
MONDO:0014429	autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency	skos:exactMatch	DOID:0111956	immunodeficiency 27B	semapv:ManualMappingCuration	2023-04-17
MONDO:0014431	LIPE-related familial partial lipodystrophy	skos:exactMatch	DOID:0070206	familial partial lipodystrophy type 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0014439	Bardet-Biedl syndrome 11	skos:exactMatch	DOID:0110133	Bardet-Biedl syndrome 11	semapv:ManualMappingCuration	2024-04-21
MONDO:0014442	Bardet-Biedl syndrome 14	skos:exactMatch	DOID:0110136	Bardet-Biedl syndrome 14	semapv:ManualMappingCuration	2024-04-21
MONDO:0014443	Bardet-Biedl syndrome 15	skos:exactMatch	DOID:0110137	Bardet-Biedl syndrome 15	semapv:ManualMappingCuration	2024-04-21
MONDO:0014444	Bardet-Biedl syndrome 16	skos:exactMatch	DOID:0110138	Bardet-Biedl syndrome 16	semapv:ManualMappingCuration	2023-03-17
MONDO:0014451	focal segmental glomerulosclerosis 7	skos:exactMatch	DOID:0111132	focal segmental glomerulosclerosis 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0014453	immunodeficiency 36	skos:exactMatch	DOID:0111949	immunodeficiency 36	semapv:ManualMappingCuration	2023-03-17
MONDO:0014456	autosomal recessive severe congenital neutropenia due to JAGN1 deficiency	skos:exactMatch	DOID:0112134	severe congenital neutropenia 6	semapv:ManualMappingCuration	2023-04-17
MONDO:0014466	Neu-Laxova syndrome 2	skos:exactMatch	DOID:0080075	Neu-Laxova syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0014467	Charcot-Marie-Tooth disease recessive intermediate D	skos:exactMatch	DOID:0110203	Charcot-Marie-Tooth disease recessive intermediate D	semapv:ManualMappingCuration	2023-11-19
MONDO:0014470	autosomal dominant nonsyndromic hearing loss 65	skos:exactMatch	DOID:0110586	autosomal dominant nonsyndromic deafness 65	semapv:ManualMappingCuration	2023-03-17
MONDO:0014471	mitochondrial proton-transporting ATP synthase complex deficiency	skos:exactMatch	DOID:0111143	mitochondrial complex V (ATP synthase) deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0014474	autosomal recessive limb-girdle muscular dystrophy type 2U	skos:exactMatch	DOID:0110295	autosomal recessive limb-girdle muscular dystrophy type 2U	semapv:ManualMappingCuration	2023-03-17
MONDO:0014476	episodic ataxia type 8	skos:exactMatch	DOID:0050996	episodic ataxia type 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0014482	intellectual disability, autosomal dominant 29	skos:exactMatch	DOID:0070059	autosomal dominant intellectual developmental disorder 29	semapv:ManualMappingCuration	2023-09-24
MONDO:0014487	congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome	skos:exactMatch	DOID:0080209	sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay	semapv:ManualMappingCuration	2023-03-17
MONDO:0014489	limb-girdle muscular dystrophy due to POMK deficiency	skos:exactMatch	DOID:0112381	muscular dystrophy-dystroglycanopathy type C12	semapv:ManualMappingCuration	2023-04-17
MONDO:0014491	immunodeficiency 37	skos:exactMatch	DOID:0111939	immunodeficiency 37	semapv:ManualMappingCuration	2024-02-18
MONDO:0014498	familial cold autoinflammatory syndrome 4	skos:exactMatch	DOID:0090065	familial cold autoinflammatory syndrome 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0014502	Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency	skos:exactMatch	DOID:0111934	immunodeficiency 38	semapv:ManualMappingCuration	2023-04-17
MONDO:0014503	autosomal recessive spinocerebellar ataxia 17	skos:exactMatch	DOID:0080064	autosomal recessive spinocerebellar ataxia 17	semapv:ManualMappingCuration	2023-11-19
MONDO:0014506	hypomyelinating leukodystrophy 9	skos:exactMatch	DOID:0060791	hypomyelinating leukodystrophy 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0014507	Catel-Manzke syndrome	skos:exactMatch	DOID:0081122	Catel Manzke syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0014510	fatty acyl-CoA reductase 1 deficiency	skos:exactMatch	DOID:0081243	rhizomelic chondrodysplasia punctate type 4	semapv:ManualMappingCuration	2023-06-18
MONDO:0014511	Charcot-Marie-Tooth disease axonal type 2S	skos:exactMatch	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S	semapv:ManualMappingCuration	2023-03-17
MONDO:0014512	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation	skos:exactMatch	DOID:0070061	autosomal dominant intellectual developmental disorder 31	semapv:ManualMappingCuration	2023-03-17
MONDO:0014518	platelet-type bleeding disorder 19	skos:exactMatch	DOID:0111048	platelet-type bleeding disorder 19	semapv:ManualMappingCuration	2023-03-17
MONDO:0014527	progeroid features-hepatocellular carcinoma predisposition syndrome	skos:exactMatch	DOID:0111264	Ruijs-Aalfs syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014528	chronic atrial and intestinal dysrhythmia	skos:exactMatch	DOID:0060339	chronic atrial and intestinal dysrhythmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0014530	autosomal recessive spinocerebellar ataxia 18	skos:exactMatch	DOID:0080042	autosomal recessive spinocerebellar ataxia 18	semapv:ManualMappingCuration	2023-03-17
MONDO:0014532	autosomal dominant mitochondrial myopathy with exercise intolerance	skos:exactMatch	DOID:0081357	isolated mitochondrial myopathy	semapv:ManualMappingCuration	2023-07-09
MONDO:0014533	developmental and epileptic encephalopathy, 28	skos:exactMatch	DOID:0080452	developmental and epileptic encephalopathy 28	semapv:ManualMappingCuration	2024-04-21
MONDO:0014539	focal segmental glomerulosclerosis 9	skos:exactMatch	DOID:0111134	focal segmental glomerulosclerosis 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0014541	motor developmental delay due to 14q32.2 paternally expressed gene defect	skos:exactMatch	DOID:0111713	Temple syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014542	congenital myasthenic syndrome 15	skos:exactMatch	DOID:0110658	congenital myasthenic syndrome 15	semapv:ManualMappingCuration	2024-05-19
MONDO:0014548	long QT syndrome 14	skos:exactMatch	DOID:0110655	long QT syndrome 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0014550	long QT syndrome 15	skos:exactMatch	DOID:0110656	long QT syndrome 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0014555	peeling skin syndrome type A	skos:exactMatch	DOID:0070522	peeling skin syndrome 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0014558	autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome	skos:exactMatch	DOID:0070062	Arboleda-Tham syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014559	progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome	skos:exactMatch	DOID:0081212	autosomal recessive intellectual developmental disorder 48	semapv:ManualMappingCuration	2023-11-19
MONDO:0014561	3-methylglutaconic aciduria, type VIIB	skos:exactMatch	DOID:0081134	3-methylglutaconic aciduria type 7b	semapv:ManualMappingCuration	2023-09-24
MONDO:0014561	3-methylglutaconic aciduria, type VIIB	skos:exactMatch	DOID:0110003	3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia	semapv:ManualMappingCuration	2023-09-24
MONDO:0014562	neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome	skos:exactMatch	DOID:0070244	primary coenzyme Q10 deficiency 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0014563	mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency	skos:exactMatch	DOID:0070540	mitochondrial short-chain enoyl-CoA hydratase 1 deficiency	semapv:ManualMappingCuration	2024-07-21
MONDO:0014564	congenital bile acid synthesis defect 5	skos:exactMatch	DOID:0111066	congenital bile acid synthesis defect 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0014566	Charcot-Marie-Tooth disease axonal type 2U	skos:exactMatch	DOID:0110173	Charcot-Marie-Tooth disease axonal type 2U	semapv:ManualMappingCuration	2023-03-17
MONDO:0014567	glutamate pyruvate transaminase 2 deficiency	skos:exactMatch	DOID:0070542	neurodevelopmental disorder with spastic paraplegia and microcephaly	semapv:ManualMappingCuration	2024-07-21
MONDO:0014568	hereditary spastic paraplegia 73	skos:exactMatch	DOID:0110818	hereditary spastic paraplegia 73	semapv:ManualMappingCuration	2023-03-17
MONDO:0014572	Lichtenstein-Knorr syndrome	skos:exactMatch	DOID:0080065	autosomal recessive spinocerebellar ataxia 19	semapv:ManualMappingCuration	2023-03-17
MONDO:0014574	peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome	skos:exactMatch	DOID:0070526	PLACK syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0014578	congenital myasthenic syndrome 17	skos:exactMatch	DOID:0110674	congenital myasthenic syndrome 17	semapv:ManualMappingCuration	2024-04-21
MONDO:0014587	congenital myasthenic syndrome 9	skos:exactMatch	DOID:0110670	congenital myasthenic syndrome 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0014589	maturity-onset diabetes of the young type 13	skos:exactMatch	DOID:0111110	maturity-onset diabetes of the young type 13	semapv:ManualMappingCuration	2024-04-21
MONDO:0014592	microcephaly and chorioretinopathy 3	skos:exactMatch	DOID:0080107	microcephaly and chorioretinopathy 3	semapv:ManualMappingCuration	2023-11-19
MONDO:0014593	developmental and epileptic encephalopathy, 29	skos:exactMatch	DOID:0080451	developmental and epileptic encephalopathy 29	semapv:ManualMappingCuration	2023-03-17
MONDO:0014597	immunodeficiency 39	skos:exactMatch	DOID:0111969	immunodeficiency 39	semapv:ManualMappingCuration	2024-02-18
MONDO:0014601	autosomal recessive spinocerebellar ataxia 20	skos:exactMatch	DOID:0080066	autosomal recessive spinocerebellar ataxia 20	semapv:ManualMappingCuration	2023-03-17
MONDO:0014602	Hogue-Janssens syndrome 1	skos:exactMatch	DOID:0070065	autosomal dominant intellectual developmental disorder 35	semapv:ManualMappingCuration	2023-11-19
MONDO:0014603	autosomal dominant nonsyndromic hearing loss 40	skos:exactMatch	DOID:0110566	autosomal dominant nonsyndromic deafness 40	semapv:ManualMappingCuration	2023-03-17
MONDO:0014605	Houge-Janssens syndrome 2	skos:exactMatch	DOID:0070066	autosomal dominant intellectual developmental disorder 36	semapv:ManualMappingCuration	2023-11-19
MONDO:0014606	intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome	skos:exactMatch	DOID:0070067	White-Sutton syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014608	mandibulofacial dysostosis with alopecia	skos:exactMatch	DOID:0060365	mandibulofacial dysostosis with alopecia	semapv:ManualMappingCuration	2023-03-17
MONDO:0014611	multiple mitochondrial dysfunctions syndrome 4	skos:exactMatch	DOID:0080136	multiple mitochondrial dysfunctions syndrome 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0014615	trichothiodystrophy 2, photosensitive	skos:exactMatch	DOID:0111869	photosensitive trichothiodystrophy 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0014618	retinitis pigmentosa 71	skos:exactMatch	DOID:0110363	retinitis pigmentosa 71	semapv:ManualMappingCuration	2023-03-17
MONDO:0014619	trichothiodystrophy 3, photosensitive	skos:exactMatch	DOID:0111871	photosensitive trichothiodystrophy 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0014620	myoclonic dystonia 26	skos:exactMatch	DOID:0090036	myoclonic dystonia 26	semapv:ManualMappingCuration	2023-09-24
MONDO:0014621	Brugada syndrome 9	skos:exactMatch	DOID:0110226	Brugada syndrome 9	semapv:ManualMappingCuration	2024-04-21
MONDO:0014629	autoimmune interstitial lung disease-arthritis syndrome	skos:exactMatch	DOID:0081242	autoimmune interstitial lung, joint, and kidney disease	semapv:ManualMappingCuration	2023-04-17
MONDO:0014632	hypomyelinating leukodystrophy 10	skos:exactMatch	DOID:0060788	hypomyelinating leukodystrophy 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0014636	combined oxidative phosphorylation defect type 25	skos:exactMatch	DOID:0111468	combined oxidative phosphorylation deficiency 25	semapv:ManualMappingCuration	2024-04-21
MONDO:0014637	DOCK2 deficiency	skos:exactMatch	DOID:0111951	immunodeficiency 40	semapv:ManualMappingCuration	2023-04-17
MONDO:0014639	familial temporal lobe epilepsy 7	skos:exactMatch	DOID:0060751	familial temporal lobe epilepsy 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0014641	frontotemporal dementia and/or amyotrophic lateral sclerosis 4	skos:exactMatch	DOID:0110069	frontotemporal dementia and/or amyotrophic lateral sclerosis 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0014644	hereditary spastic paraplegia 74	skos:exactMatch	DOID:0110819	hereditary spastic paraplegia 74	semapv:ManualMappingCuration	2023-03-17
MONDO:0014654	Ullrich congenital muscular dystrophy 2	skos:exactMatch	DOID:0060948	Ullrich congenital muscular dystrophy 2	semapv:ManualMappingCuration	2024-07-21
MONDO:0014656	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2	skos:exactMatch	DOID:0111515	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0014658	severe achondroplasia-developmental delay-acanthosis nigricans syndrome	skos:exactMatch	DOID:0111158	SADDAN	semapv:ManualMappingCuration	2023-03-17
MONDO:0014662	congenital insensitivity to pain-hypohidrosis syndrome	skos:exactMatch	DOID:0070153	hereditary sensory and autonomic neuropathy type 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0014664	Joubert syndrome 23	skos:exactMatch	DOID:0110992	Joubert syndrome 23	semapv:ManualMappingCuration	2024-04-21
MONDO:0014665	Charcot-Marie-Tooth disease axonal type 2V	skos:exactMatch	DOID:0110178	Charcot-Marie-Tooth disease axonal type 2V	semapv:ManualMappingCuration	2023-03-17
MONDO:0014678	intellectual disability, autosomal dominant 39	skos:exactMatch	DOID:0070069	autosomal dominant intellectual developmental disorder 39	semapv:ManualMappingCuration	2023-03-17
MONDO:0014683	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9	skos:exactMatch	DOID:0111232	congenital muscular dystrophy-dystroglycanopathy type A9	semapv:ManualMappingCuration	2023-03-17
MONDO:0014687	retinitis pigmentosa 73	skos:exactMatch	DOID:0110389	retinitis pigmentosa 73	semapv:ManualMappingCuration	2024-04-21
MONDO:0014688	short-rib thoracic dysplasia 14 with polydactyly	skos:exactMatch	DOID:0110096	short-rib thoracic dysplasia 14 with polydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0014689	Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome	skos:exactMatch	DOID:0080592	Klippel-Feil syndrome 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0014699	intellectual disability, autosomal dominant 40	skos:exactMatch	DOID:0070070	autosomal dominant intellectual developmental disorder 40	semapv:ManualMappingCuration	2023-11-19
MONDO:0014701	spondyloepiphyseal dysplasia, Stanescu type	skos:exactMatch	DOID:0112281	spondyloepiphyseal dysplasia Stanescu type	semapv:ManualMappingCuration	2023-06-18
MONDO:0014702	autosomal recessive complex spastic paraplegia type 9B	skos:exactMatch	DOID:0110825	hereditary spastic paraplegia 9B	semapv:ManualMappingCuration	2023-11-19
MONDO:0014706	cutis laxa, autosomal dominant 3	skos:exactMatch	DOID:0070131	autosomal dominant cutis laxa 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0014710	autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency	skos:exactMatch	DOID:0111940	immunodeficiency 42	semapv:ManualMappingCuration	2023-04-17
MONDO:0014711	autosomal dominant Charcot-Marie-Tooth disease type 2W	skos:exactMatch	DOID:0110162	Charcot-Marie-Tooth disease, axonal type 2W	semapv:ManualMappingCuration	2023-03-17
MONDO:0014715	primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection	skos:exactMatch	DOID:0111975	immunodeficiency 44	semapv:ManualMappingCuration	2023-04-17
MONDO:0014717	early-onset Lafora body disease	skos:exactMatch	DOID:0111445	progressive myoclonus epilepsy 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0014719	developmental and epileptic encephalopathy, 35	skos:exactMatch	DOID:0080458	developmental and epileptic encephalopathy 35	semapv:ManualMappingCuration	2023-11-19
MONDO:0014720	autosomal dominant optic atrophy plus syndrome	skos:exactMatch	DOID:0111340	dominant optic atrophy plus syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0014725	spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome	skos:exactMatch	DOID:0070537	spastic tetraplegia, thin corpus callosum, and progressive microcephaly	semapv:ManualMappingCuration	2024-04-21
MONDO:0014727	immunodeficiency 45	skos:exactMatch	DOID:0111994	immunodeficiency 45	semapv:ManualMappingCuration	2024-02-18
MONDO:0014732	hypomyelinating leukodystrophy 12	skos:exactMatch	DOID:0060796	hypomyelinating leukodystrophy 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0014733	Charcot-Marie-Tooth disease type 4K	skos:exactMatch	DOID:0110187	Charcot-Marie-Tooth disease type 4K	semapv:ManualMappingCuration	2023-03-17
MONDO:0014735	Charcot-Marie-Tooth disease type 2Y	skos:exactMatch	DOID:0110168	Charcot-Marie-Tooth disease type 2Y	semapv:ManualMappingCuration	2023-11-19
MONDO:0014736	Charcot-Marie-Tooth disease axonal type 2Z	skos:exactMatch	DOID:0110181	Charcot-Marie-Tooth disease axonal type 2Z	semapv:ManualMappingCuration	2023-03-17
MONDO:0014738	autosomal dominant nonsyndromic hearing loss 69	skos:exactMatch	DOID:0110590	autosomal dominant nonsyndromic deafness 69	semapv:ManualMappingCuration	2024-04-21
MONDO:0014743	rhizomelic chondrodysplasia punctata type 5	skos:exactMatch	DOID:0110854	rhizomelic chondrodysplasia punctata type 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0014744	acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome	skos:exactMatch	DOID:0111155	autosomal recessive spinocerebellar ataxia 21	semapv:ManualMappingCuration	2023-11-19
MONDO:0014746	SLC39A8-CDG	skos:exactMatch	DOID:0070266	congenital disorder of glycosylation type IIn	semapv:ManualMappingCuration	2023-03-17
MONDO:0014754	primary coenzyme Q10 deficiency 8	skos:exactMatch	DOID:0070245	primary coenzyme Q10 deficiency 8	semapv:ManualMappingCuration	2023-11-19
MONDO:0014760	TFRC-related combined immunodeficiency	skos:exactMatch	DOID:0111948	immunodeficiency 46	semapv:ManualMappingCuration	2023-11-19
MONDO:0014765	wooly hair, autosomal recessive 3	skos:exactMatch	DOID:0111574	autosomal recessive woolly hair 3	semapv:ManualMappingCuration	2024-02-18
MONDO:0014768	cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2	skos:exactMatch	DOID:0111036	CADASIL2	semapv:ManualMappingCuration	2023-03-17
MONDO:0014772	orofacial cleft 15	skos:exactMatch	DOID:0080408	orofacial cleft 15	semapv:ManualMappingCuration	2023-11-19
MONDO:0014782	autosomal recessive limb-girdle muscular dystrophy type 2X	skos:exactMatch	DOID:0110290	autosomal recessive limb-girdle muscular dystrophy type 2X	semapv:ManualMappingCuration	2023-03-17
MONDO:0014788	autosomal recessive limb-girdle muscular dystrophy type 2W	skos:exactMatch	DOID:0110288	autosomal recessive limb-girdle muscular dystrophy type 2W	semapv:ManualMappingCuration	2023-03-17
MONDO:0014789	CCDC115-CDG	skos:exactMatch	DOID:0070267	congenital disorder of glycosylation type IIo	semapv:ManualMappingCuration	2023-03-17
MONDO:0014790	TMEM199-CDG	skos:exactMatch	DOID:0070268	congenital disorder of glycosylation type IIp	semapv:ManualMappingCuration	2023-03-17
MONDO:0014802	Cowden syndrome 7	skos:exactMatch	DOID:0081003	Cowden syndrome 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0014804	sideroblastic anemia 3	skos:exactMatch	DOID:0080343	autosomal recessive pyridoxine-refractory sideroblastic anemia 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0014810	pancytopenia due to IKZF1 mutations	skos:exactMatch	DOID:0081155	common variable immunodeficiency 13	semapv:ManualMappingCuration	2023-06-18
MONDO:0014811	cerebellar atrophy, visual impairment, and psychomotor retardation;	skos:exactMatch	DOID:0081276	cerebellar atrophy, visual impairment, and psychomotor retardation	semapv:ManualMappingCuration	2023-11-19
MONDO:0014813	hypomyelinating leukodystrophy 13	skos:exactMatch	DOID:0060795	hypomyelinating leukodystrophy 13	semapv:ManualMappingCuration	2023-03-17
MONDO:0014820	mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)	skos:exactMatch	DOID:0080336	mitochondrial DNA depletion syndrome 14	semapv:ManualMappingCuration	2023-03-17
MONDO:0014836	Charcot-Marie-Tooth disease axonal type 2CC	skos:exactMatch	DOID:0110180	Charcot-Marie-Tooth disease axonal type 2CC	semapv:ManualMappingCuration	2023-03-17
MONDO:0014842	intellectual disability, autosomal dominant 41	skos:exactMatch	DOID:0070071	autosomal dominant intellectual developmental disorder 41	semapv:ManualMappingCuration	2023-03-17
MONDO:0014843	premature ovarian failure 11	skos:exactMatch	DOID:0080868	primary ovarian insufficiency 11	semapv:ManualMappingCuration	2024-04-21
MONDO:0014843	premature ovarian failure 11	skos:exactMatch	DOID:0080869	primary ovarian insufficiency 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0014846	spinocerebellar ataxia, autosomal recessive 23	skos:exactMatch	DOID:0111613	autosomal recessive spinocerebellar ataxia 23	semapv:ManualMappingCuration	2023-03-17
MONDO:0014847	spermatogenic failure 15	skos:exactMatch	DOID:0070172	spermatogenic failure 15	semapv:ManualMappingCuration	2023-03-17
MONDO:0014853	autosomal dominant nonsyndromic hearing loss 70	skos:exactMatch	DOID:0110592	autosomal dominant nonsyndromic deafness 70	semapv:ManualMappingCuration	2023-03-17
MONDO:0014855	intellectual disability, autosomal dominant 42	skos:exactMatch	DOID:0070072	autosomal dominant intellectual developmental disorder 42	semapv:ManualMappingCuration	2023-11-19
MONDO:0014858	intellectual disability, autosomal dominant 43	skos:exactMatch	DOID:0070073	autosomal dominant intellectual developmental disorder 43	semapv:ManualMappingCuration	2023-09-24
MONDO:0014864	hypermanganesemia with dystonia 2	skos:exactMatch	DOID:0080537	hypermanganesemia with dystonia 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0014865	autosomal recessive severe congenital neutropenia due to CSF3R deficiency	skos:exactMatch	DOID:0112129	severe congenital neutropenia 7	semapv:ManualMappingCuration	2023-04-17
MONDO:0014866	Charcot-Marie-Tooth disease axonal type 2T	skos:exactMatch	DOID:0110160	Charcot-Marie-Tooth disease axonal type 2T	semapv:ManualMappingCuration	2024-04-21
MONDO:0014867	spinocerebellar ataxia 43	skos:exactMatch	DOID:0111745	cerebellar ataxia type 43	semapv:ManualMappingCuration	2024-04-21
MONDO:0014872	congenital stationary night blindness 1H	skos:exactMatch	DOID:0110866	congenital stationary night blindness 1H	semapv:ManualMappingCuration	2023-11-19
MONDO:0014882	hereditary spastic paraplegia 77	skos:exactMatch	DOID:0110822	hereditary spastic paraplegia 77	semapv:ManualMappingCuration	2023-03-17
MONDO:0014883	hypertrophic cardiomyopathy 26	skos:exactMatch	DOID:0110327	hypertrophic cardiomyopathy 26	semapv:ManualMappingCuration	2023-03-17
MONDO:0014892	micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome	skos:exactMatch	DOID:0070074	autosomal dominant intellectual developmental disorder 44	semapv:ManualMappingCuration	2023-03-17
MONDO:0014898	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3	skos:exactMatch	DOID:0111523	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0014899	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4	skos:exactMatch	DOID:0111516	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0014900	autosomal recessive limb-girdle muscular dystrophy type 2Y	skos:exactMatch	DOID:0110289	autosomal recessive limb-girdle muscular dystrophy type 2Y	semapv:ManualMappingCuration	2023-03-17
MONDO:0014903	seizures, benign familial infantile, 5	skos:exactMatch	DOID:0081118	benign familial infantile seizures 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0014906	Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;	skos:exactMatch	DOID:0111557	Charcot-Marie-Tooth disease type 2A2B	semapv:ManualMappingCuration	2023-11-19
MONDO:0014912	infantile-onset periodic fever-panniculitis-dermatosis syndrome	skos:exactMatch	DOID:0080163	otulipenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0014916	developmental and epileptic encephalopathy, 41	skos:exactMatch	DOID:0080442	developmental and epileptic encephalopathy 41	semapv:ManualMappingCuration	2023-03-17
MONDO:0014917	developmental and epileptic encephalopathy, 42	skos:exactMatch	DOID:0080454	developmental and epileptic encephalopathy 42	semapv:ManualMappingCuration	2024-04-21
MONDO:0014920	patterned macular dystrophy 3	skos:exactMatch	DOID:0060865	patterned macular dystrophy 3	semapv:ManualMappingCuration	2023-11-19
MONDO:0014921	developmental and epileptic encephalopathy, 43	skos:exactMatch	DOID:0080447	developmental and epileptic encephalopathy 43	semapv:ManualMappingCuration	2023-11-19
MONDO:0014922	myofibrillar myopathy 7	skos:exactMatch	DOID:0080098	myofibrillar myopathy 7	semapv:ManualMappingCuration	2023-11-19
MONDO:0014930	intellectual disability, autosomal recessive 56	skos:exactMatch	DOID:0081217	autosomal recessive intellectual developmental disorder 56	semapv:ManualMappingCuration	2023-06-18
MONDO:0014933	developmental and epileptic encephalopathy, 44	skos:exactMatch	DOID:0080424	developmental and epileptic encephalopathy 44	semapv:ManualMappingCuration	2023-11-19
MONDO:0014934	spinocerebellar ataxia, autosomal recessive 24	skos:exactMatch	DOID:0111615	autosomal recessive spinocerebellar ataxia 24	semapv:ManualMappingCuration	2024-04-21
MONDO:0014935	frontometaphyseal dysplasia 2	skos:exactMatch	DOID:0111787	frontometaphyseal dysplasia 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0014940	neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset	skos:exactMatch	DOID:0081364	neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset	semapv:ManualMappingCuration	2023-07-09
MONDO:0014942	developmental and epileptic encephalopathy, 45	skos:exactMatch	DOID:0080428	developmental and epileptic encephalopathy 45	semapv:ManualMappingCuration	2023-11-19
MONDO:0014943	mitochondrial DNA depletion syndrome 15 (hepatocerebral type)	skos:exactMatch	DOID:0080337	mitochondrial DNA depletion syndrome 15	semapv:ManualMappingCuration	2023-09-24
MONDO:0014946	Sifrim-Hitz-Weiss syndrome	skos:exactMatch	DOID:0070529	Sifrim-Hitz-Weiss syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0014947	developmental and epileptic encephalopathy, 46	skos:exactMatch	DOID:0080456	developmental and epileptic encephalopathy 46	semapv:ManualMappingCuration	2023-11-19
MONDO:0014951	intellectual developmental disorder, autosomal recessive 74	skos:exactMatch	DOID:0081218	autosomal recessive intellectual developmental disorder 74	semapv:ManualMappingCuration	2023-11-19
MONDO:0014951	intellectual developmental disorder, autosomal recessive 74	skos:exactMatch	DOID:0112104	Sotos syndrome 3	semapv:ManualMappingCuration	2023-11-19
MONDO:0014953	gnb5-related intellectual disability-cardiac arrhythmia syndrome	skos:exactMatch	DOID:0081008	intellectual developmental disorder with cardiac arrhythmia	semapv:ManualMappingCuration	2023-04-17
MONDO:0014954	Ehlers-Danlos syndrome, periodontal type 2	skos:exactMatch	DOID:0080987	Ehlers-Danlos syndrome periodontal type 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0014958	Harel-Yoon syndrome	skos:exactMatch	DOID:0081395	Harel-Yoon syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0014959	mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant	skos:exactMatch	DOID:0080130	mitochondrial DNA depletion syndrome 12a	semapv:ManualMappingCuration	2023-03-17
MONDO:0014962	intellectual disability, autosomal recessive 57	skos:exactMatch	DOID:0081219	autosomal recessive intellectual developmental disorder 57	semapv:ManualMappingCuration	2023-06-18
MONDO:0014975	autosomal recessive spastic paraplegia type 78	skos:exactMatch	DOID:0112348	hereditary spastic paraplegia 78	semapv:ManualMappingCuration	2023-06-18
MONDO:0014981	immunodeficiency 49	skos:exactMatch	DOID:0111979	immunodeficiency 49	semapv:ManualMappingCuration	2024-02-18
MONDO:0014985	Fanconi anemia complementation group V	skos:exactMatch	DOID:0111080	Fanconi anemia complementation group V	semapv:ManualMappingCuration	2023-11-19
MONDO:0014986	Fanconi anemia complementation group R	skos:exactMatch	DOID:0111090	Fanconi anemia complementation group R	semapv:ManualMappingCuration	2023-11-19
MONDO:0014987	Fanconi anemia complementation group U	skos:exactMatch	DOID:0111085	Fanconi anemia complementation group U	semapv:ManualMappingCuration	2023-11-19
MONDO:0014993	myofibrillar myopathy 8	skos:exactMatch	DOID:0080308	myofibrillar myopathy 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0014996	intellectual disability, autosomal recessive 58	skos:exactMatch	DOID:0081220	autosomal recessive intellectual developmental disorder 58	semapv:ManualMappingCuration	2023-06-18
MONDO:0015000	developmental and epileptic encephalopathy, 48	skos:exactMatch	DOID:0080448	developmental and epileptic encephalopathy 48	semapv:ManualMappingCuration	2023-11-19
MONDO:0015003	dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	skos:exactMatch	DOID:0081419	childhood-onset dystonia with optic atrophy and basal ganglia abnormalities	semapv:ManualMappingCuration	2024-04-21
MONDO:0015020	intellectual disability, autosomal recessive 59	skos:exactMatch	DOID:0081221	autosomal recessive intellectual developmental disorder 59	semapv:ManualMappingCuration	2023-11-19
MONDO:0015023	MYPN-related myopathy	skos:exactMatch	DOID:0110933	nemaline myopathy 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0015025	developmental and epileptic encephalopathy, 51	skos:exactMatch	DOID:0080433	developmental and epileptic encephalopathy 51	semapv:ManualMappingCuration	2023-11-19
MONDO:0015032	intraneural perineurioma	skos:exactMatch	DOID:4696	intraneural perineurioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0015059	progressive non-fluent aphasia	skos:exactMatch	DOID:0081390	progressive non-fluent aphasia	semapv:ManualMappingCuration	2024-04-21
MONDO:0015070	laryngeal neuroendocrine neoplasm	skos:exactMatch	DOID:5457	laryngeal neuroendocrine tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0015104	porphyria cutanea tarda	skos:exactMatch	DOID:3132	porphyria cutanea tarda	semapv:ManualMappingCuration	2023-03-17
MONDO:0015129	chronic primary adrenal insufficiency	skos:exactMatch	DOID:13774	Addison's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0015131	combined immunodeficiency	skos:exactMatch	DOID:0111962	combined immunodeficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015131	combined immunodeficiency	skos:exactMatch	DOID:628	combined T cell and B cell immunodeficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015148	lissencephaly type 3	skos:exactMatch	DOID:0112232	lissencephaly 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0015151	muscular dystrophy, limb-girdle, autosomal dominant	skos:exactMatch	DOID:0110273	autosomal dominant limb-girdle muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015152	autosomal recessive limb-girdle muscular dystrophy	skos:exactMatch	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015168	arthrogryposis multiplex congenita	skos:exactMatch	DOID:0080954	arthrogryposis multiplex congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0015175	autoimmune pancreatitis	skos:exactMatch	DOID:0040091	autoimmune pancreatitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015183	short bowel syndrome	skos:exactMatch	DOID:10605	short bowel syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015194	sideroblastic anemia	skos:exactMatch	DOID:8955	sideroblastic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015204	microlissencephaly	skos:exactMatch	DOID:0112234	microlissencephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0015229	Bardet-Biedl syndrome	skos:exactMatch	DOID:1935	Bardet-Biedl syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015231	Bartter syndrome	skos:exactMatch	DOID:445	Bartter disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0015240	digitotalar dysmorphism	skos:exactMatch	DOID:0111596	distal arthrogryposis type 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0015244	autosomal recessive cerebellar ataxia	skos:exactMatch	DOID:0050950	autosomal recessive cerebellar ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015253	Diamond-Blackfan anemia	skos:exactMatch	DOID:1339	Diamond-Blackfan anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015262	brachyolmia	skos:exactMatch	DOID:0050690	brachyolmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015263	Brugada syndrome	skos:exactMatch	DOID:0050451	Brugada syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015267	Feingold syndrome	skos:exactMatch	DOID:0060464	Feingold syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015277	medullary thyroid gland carcinoma	skos:exactMatch	DOID:3973	medullary thyroid carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0015279	chronic mucocutaneous candidiasis	skos:exactMatch	DOID:2058	chronic mucocutaneous candidiasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015280	cardiofaciocutaneous syndrome	skos:exactMatch	DOID:0060233	cardiofaciocutaneous syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015285	Carney complex	skos:exactMatch	DOID:0050471	Carney complex	semapv:ManualMappingCuration	2023-03-17
MONDO:0015286	congenital disorder of glycosylation	skos:exactMatch	DOID:5212	congenital disorder of glycosylation	semapv:ManualMappingCuration	2023-03-17
MONDO:0015301	primary cutaneous amyloidosis	skos:exactMatch	DOID:0050639	primary cutaneous amyloidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015333	progeroid syndrome	skos:exactMatch	DOID:0081332	progeroid syndrome	semapv:ManualMappingCuration	2023-05-21
MONDO:0015352	distal hereditary motor neuropathy type 2	skos:exactMatch	DOID:0111206	autosomal dominant distal hereditary motor neuronopathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0015353	neuronopathy, distal hereditary motor, type 5A	skos:exactMatch	DOID:0111204	distal hereditary motor neuronopathy type 5A	semapv:ManualMappingCuration	2023-03-17
MONDO:0015355	distal hereditary motor neuropathy type 7	skos:exactMatch	DOID:0111199	autosomal dominant distal hereditary motor neuronopathy 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0015362	neuronopathy, distal hereditary motor, autosomal dominant	skos:exactMatch	DOID:0111198	autosomal dominant distal hereditary motor neuronopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015363	neuronopathy, distal hereditary motor, autosomal recessive	skos:exactMatch	DOID:0111197	autosomal recessive distal hereditary motor neuronopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015364	hereditary sensory and autonomic neuropathy	skos:exactMatch	DOID:0050548	hereditary sensory neuropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015375	orofaciodigital syndrome	skos:exactMatch	DOID:4501	orofaciodigital syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015397	craniofacial microsomia	skos:exactMatch	DOID:2907	Goldenhar syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015426	Desbuquois dysplasia	skos:exactMatch	DOID:0060462	Desbuquois dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015448	mitochondrial complex III deficiency	skos:exactMatch	DOID:0111139	mitochondrial complex III deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015452	Coffin-Siris syndrome	skos:exactMatch	DOID:1925	Coffin-Siris syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015454	multiple carboxylase deficiency	skos:exactMatch	DOID:857	multiple carboxylase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015459	nasopharyngeal carcinoma	skos:exactMatch	DOID:9261	nasopharynx carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0015465	craniometaphyseal dysplasia	skos:exactMatch	DOID:0080033	craniometaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015469	craniosynostosis	skos:exactMatch	DOID:2340	craniosynostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015474	cryptosporidiosis	skos:exactMatch	DOID:1733	cryptosporidiosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015486	keratoconus	skos:exactMatch	DOID:10126	keratoconus	semapv:ManualMappingCuration	2023-03-17
MONDO:0015487	fatal infantile encephalocardiomyopathy	skos:exactMatch	DOID:0050713	COX deficiency, infantile mitochondrial myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015515	carnitine palmitoyltransferase II deficiency	skos:exactMatch	DOID:0060235	carnitine palmitoyltransferase II deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015517	common variable immunodeficiency	skos:exactMatch	DOID:12177	common variable immunodeficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015523	epithelioid hemangioendothelioma	skos:exactMatch	DOID:0080190	malignant epithelioid hemangioendothelioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0015526	cold-induced sweating syndrome	skos:exactMatch	DOID:0060294	cold-induced sweating syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015528	congenital epulis	skos:exactMatch	DOID:7280	congenital epulis	semapv:ManualMappingCuration	2024-05-19
MONDO:0015528	congenital epulis	skos:exactMatch	DOID:8303	congenital granular cell tumor	semapv:ManualMappingCuration	2024-05-19
MONDO:0015531	non-Langerhans cell histiocytosis	skos:exactMatch	DOID:4330	non-Langerhans-cell histiocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015540	hemophagocytic syndrome	skos:exactMatch	DOID:0050120	hemophagocytic lymphohistiocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015564	Castleman disease	skos:exactMatch	DOID:0111157	Castleman disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0015597	pustulosis palmaris et plantaris	skos:exactMatch	DOID:4398	pustulosis of palm and sole	semapv:ManualMappingCuration	2023-03-17
MONDO:0015601	X-linked intellectual disability, van Esch type	skos:exactMatch	DOID:0111840	Van Esch-O'Driscoll syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0015609	advanced sleep phase syndrome	skos:exactMatch	DOID:0050628	advanced sleep phase syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015611	neutral lipid storage disease	skos:exactMatch	DOID:0050729	Chanarin-Dorfman syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015612	Dent disease	skos:exactMatch	DOID:0050699	Dent disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0015613	dentin dysplasia	skos:exactMatch	DOID:701	dentin dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015626	Charcot-Marie-Tooth disease	skos:exactMatch	DOID:10595	Charcot-Marie-Tooth disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0015627	multiple epiphyseal dysplasia due to collagen 9 anomaly	skos:exactMatch	DOID:0070305	multiple epiphyseal dysplasia due to collagen 9 anomaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0015643	photosensitive epilepsy	skos:exactMatch	DOID:0060281	photosensitive epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015681	childhood disintegrative disorder	skos:exactMatch	DOID:13487	childhood disintegrative disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0015688	myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2	skos:exactMatch	DOID:0080164	myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1	semapv:ManualMappingCuration	2023-11-19
MONDO:0015690	myeloid neoplasm associated with PDGFRB rearrangement	skos:exactMatch	DOID:0080166	myeloid and lymphoid neoplasms associated with PDGFRB rearrangement	semapv:ManualMappingCuration	2023-11-19
MONDO:0015698	transient hypogammaglobulinemia of infancy	skos:exactMatch	DOID:624	transient hypogammaglobulinemia of infancy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015701	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency	skos:exactMatch	DOID:0060015	interleukin-7 receptor alpha deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015702	T-B+ severe combined immunodeficiency due to CD45 deficiency	skos:exactMatch	DOID:0060014	CD45 deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015705	autosomal recessive centronuclear myopathy	skos:exactMatch	DOID:0111216	autosomal recessive centronuclear myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015722	congenital vitamin K-dependent coagulation factors deficiency	skos:exactMatch	DOID:0112172	hereditary combined deficiency of vitamin K-dependent clotting factors	semapv:ManualMappingCuration	2023-08-20
MONDO:0015746	male infertility due to globozoospermia	skos:exactMatch	DOID:0112312	male infertility due to globozoospermia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015748	hereditary mucosal leukokeratosis	skos:exactMatch	DOID:0050448	white sponge nevus	semapv:ManualMappingCuration	2023-03-17
MONDO:0015760	T-cell non-Hodgkin lymphoma	skos:exactMatch	DOID:0081312	T-cell non-Hodgkin lymphoma	semapv:ManualMappingCuration	2023-04-17
MONDO:0015762	progressive familial intrahepatic cholestasis	skos:exactMatch	DOID:0070221	progressive familial intrahepatic cholestasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015776	rhizomelic chondrodysplasia punctata	skos:exactMatch	DOID:2580	rhizomelic chondrodysplasia punctata	semapv:ManualMappingCuration	2023-03-17
MONDO:0015779	45,X/46,XY mixed gonadal dysgenesis	skos:exactMatch	DOID:0080656	45,X/46,XY mixed gonadal dysgenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015780	dyskeratosis congenita	skos:exactMatch	DOID:2729	dyskeratosis congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0015797	UV-sensitive syndrome	skos:exactMatch	DOID:0060240	UV-sensitive syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0015798	inflammatory myofibroblastic tumor	skos:exactMatch	DOID:0050905	inflammatory myofibroblastic tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0015799	Smith-McCort dysplasia	skos:exactMatch	DOID:0060247	Smith-McCort dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015802	autosomal dominant non-syndromic intellectual disability	skos:exactMatch	DOID:0060307	autosomal dominant intellectual developmental disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0015804	infant botulism	skos:exactMatch	DOID:0050354	infant botulism	semapv:ManualMappingCuration	2024-04-21
MONDO:0015805	intestinal botulism	skos:exactMatch	DOID:0050141	intestinal botulism	semapv:ManualMappingCuration	2024-04-21
MONDO:0015864	mixed germ cell tumor	skos:exactMatch	DOID:3306	mixed germ cell cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0015867	vaginal carcinoma	skos:exactMatch	DOID:0050918	vaginal carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0015871	benign breast phyllodes tumor	skos:exactMatch	DOID:1631	benign breast phyllodes tumor	semapv:ManualMappingCuration	2024-04-21
MONDO:0015909	aplastic anemia	skos:exactMatch	DOID:12449	aplastic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015926	pneumoconiosis	skos:exactMatch	DOID:10316	pneumoconiosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015942	frontometaphyseal dysplasia	skos:exactMatch	DOID:0111785	frontometaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015974	severe combined immunodeficiency	skos:exactMatch	DOID:627	severe combined immunodeficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0015977	agammaglobulinemia	skos:exactMatch	DOID:2583	agammaglobulinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015986	bilateral renal agenesis	skos:exactMatch	DOID:0080200	bilateral renal aplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015991	citrullinemia	skos:exactMatch	DOID:9273	citrullinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0015993	cone-rod dystrophy	skos:exactMatch	DOID:0050572	cone-rod dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0015998	isolated ectopia lentis	skos:exactMatch	DOID:0111148	isolated ectopia lentis	semapv:ManualMappingCuration	2023-03-17
MONDO:0015999	primary pigmented nodular adrenocortical disease	skos:exactMatch	DOID:0060280	primary pigmented nodular adrenocortical disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0016001	2-hydroxyglutaric aciduria	skos:exactMatch	DOID:0050573	2-hydroxyglutaric aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0016002	Ehlers-Danlos syndrome, kyphoscoliotic type 1	skos:exactMatch	DOID:0080734	Ehlers-Danlos syndrome kyphoscoliotic type 1	semapv:ManualMappingCuration	2023-06-18
MONDO:0016006	Cockayne syndrome	skos:exactMatch	DOID:2962	Cockayne syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016022	early myoclonic encephalopathy	skos:exactMatch	DOID:308	early myoclonic encephalopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0016027	benign neonatal seizures	skos:exactMatch	DOID:14264	benign neonatal seizures	semapv:ManualMappingCuration	2023-03-17
MONDO:0016027	benign neonatal seizures	skos:exactMatch	DOID:14777	benign familial neonatal epilepsy	semapv:ManualMappingCuration	2024-04-21
MONDO:0016028	erythromelalgia	skos:exactMatch	DOID:9240	erythromelalgia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016030	Evans syndrome	skos:exactMatch	DOID:8931	Evans' syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016033	Cornelia de Lange syndrome	skos:exactMatch	DOID:11725	Cornelia de Lange syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016047	endophthalmitis	skos:exactMatch	DOID:4692	endophthalmitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016052	atypical autism	skos:exactMatch	DOID:0060042	atypical autism	semapv:ManualMappingCuration	2023-03-17
MONDO:0016056	isolated congenital microcephaly	skos:exactMatch	DOID:0070297	primary microcephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0016063	Cowden disease	skos:exactMatch	DOID:6457	Cowden syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016064	cleft palate	skos:exactMatch	DOID:674	cleft palate	semapv:ManualMappingCuration	2023-03-17
MONDO:0016068	fibrochondrogenesis	skos:exactMatch	DOID:0060465	fibrochondrogenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016070	hereditary gingival fibromatosis	skos:exactMatch	DOID:0060466	gingival fibromatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016073	syndromic microphthalmia	skos:exactMatch	DOID:0080636	syndromic microphthalmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016075	filariasis	skos:exactMatch	DOID:1080	filariasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016085	Cole-Carpenter syndrome	skos:exactMatch	DOID:0060438	Cole-Carpenter syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016103	isolated asymptomatic elevation of creatine phosphokinase	skos:exactMatch	DOID:0111338	isolated elevated serum creatine phosphokinase levels	semapv:ManualMappingCuration	2023-03-17
MONDO:0016107	myotonic dystrophy	skos:exactMatch	DOID:450	myotonic disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0016129	eosinophilic gastroenteritis	skos:exactMatch	DOID:4031	eosinophilic gastroenteritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0016162	bilateral frontal polymicrogyria	skos:exactMatch	DOID:0080921	bilateral frontal polymicrogyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0016163	autosomal dominant cerebellar ataxia type II	skos:exactMatch	DOID:0050958	spinocerebellar ataxia type 7	semapv:ManualMappingCuration	2023-04-17
MONDO:0016175	cutis laxa	skos:exactMatch	DOID:3144	cutis laxa	semapv:ManualMappingCuration	2023-03-17
MONDO:0016215	spastic quadriplegic cerebral palsy	skos:exactMatch	DOID:10970	spastic quadriplegic cerebral palsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0016216	adult hepatocellular carcinoma	skos:exactMatch	DOID:0070328	adult hepatocellular carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0016222	spindle cell hemangioma	skos:exactMatch	DOID:496	spindle cell hemangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016227	hereditary episodic ataxia	skos:exactMatch	DOID:963	episodic ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016239	cystinosis	skos:exactMatch	DOID:1064	cystinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016241	alternating hemiplegia of childhood	skos:exactMatch	DOID:0050635	alternating hemiplegia of childhood	semapv:ManualMappingCuration	2023-03-17
MONDO:0016242	hemoglobin C disease	skos:exactMatch	DOID:2859	hemoglobin C disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0016243	hemoglobin E disease	skos:exactMatch	DOID:5379	hemoglobin E disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0016244	atypical hemolytic-uremic syndrome	skos:exactMatch	DOID:0080301	atypical hemolytic-uremic syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016256	Hennekam syndrome	skos:exactMatch	DOID:0060366	Hennekam syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016293	congenital stationary night blindness	skos:exactMatch	DOID:0050534	congenital stationary night blindness	semapv:ManualMappingCuration	2023-03-17
MONDO:0016295	neuronal ceroid lipofuscinosis	skos:exactMatch	DOID:14503	neuronal ceroid lipofuscinosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016296	holoprosencephaly	skos:exactMatch	DOID:4621	holoprosencephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0016344	hydranencephaly	skos:exactMatch	DOID:4626	hydranencephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0016358	limited cutaneous systemic sclerosis	skos:exactMatch	DOID:1577	limited scleroderma	semapv:ManualMappingCuration	2023-11-19
MONDO:0016383	nephrogenic diabetes insipidus	skos:exactMatch	DOID:12387	nephrogenic diabetes insipidus	semapv:ManualMappingCuration	2023-03-17
MONDO:0016390	familial hypoparathyroidism	skos:exactMatch	DOID:0111387	familial isolated hypoparathyroidism	semapv:ManualMappingCuration	2023-03-17
MONDO:0016391	neonatal diabetes mellitus	skos:exactMatch	DOID:11717	neonatal diabetes	semapv:ManualMappingCuration	2023-03-17
MONDO:0016396	pontocerebellar hypoplasia type 1	skos:exactMatch	DOID:0112322	pontocerebellar hypoplasia type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0016471	pachyonychia congenita	skos:exactMatch	DOID:0050449	pachyonychia congenita	semapv:ManualMappingCuration	2023-03-17
MONDO:0016474	drug-induced lupus erythematosus	skos:exactMatch	DOID:0040093	drug-induced lupus erythematosus	semapv:ManualMappingCuration	2023-03-17
MONDO:0016483	intracranial berry aneurysm	skos:exactMatch	DOID:0060228	intracranial berry aneurysm	semapv:ManualMappingCuration	2023-03-17
MONDO:0016484	Usher syndrome type 2	skos:exactMatch	DOID:0110827	Usher syndrome type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0016485	Usher syndrome type 3	skos:exactMatch	DOID:0110828	Usher syndrome type 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0016486	beta-thalassemia major	skos:exactMatch	DOID:0080771	beta-thalassemia major	semapv:ManualMappingCuration	2023-03-17
MONDO:0016487	beta-thalassemia intermedia	skos:exactMatch	DOID:0080772	beta-thalassemia intermedia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016489	delta-beta-thalassemia	skos:exactMatch	DOID:0080773	delta beta-thalassemia	semapv:ManualMappingCuration	2023-06-18
MONDO:0016512	Kabuki syndrome	skos:exactMatch	DOID:0060473	Kabuki syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016516	Kenny-Caffey syndrome	skos:exactMatch	DOID:0080724	Kenny-Caffey syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016532	Lennox-Gastaut syndrome	skos:exactMatch	DOID:0050561	Lennox-Gastaut syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016535	hypohidrotic ectodermal dysplasia	skos:exactMatch	DOID:14793	hypohidrotic ectodermal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016537	lymphoproliferative syndrome	skos:exactMatch	DOID:0060704	lymphoproliferative syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016558	familial congenital mirror movements	skos:exactMatch	DOID:0111153	congenital mirror movement disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0016575	primary ciliary dyskinesia	skos:exactMatch	DOID:0050144	Kartagener syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016575	primary ciliary dyskinesia	skos:exactMatch	DOID:9562	primary ciliary dyskinesia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016576	split hand-foot malformation	skos:exactMatch	DOID:0090020	split hand-foot malformation	semapv:ManualMappingCuration	2023-03-17
MONDO:0016584	mandibuloacral dysplasia	skos:exactMatch	DOID:0081127	mandibuloacral dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016586	systemic mastocytosis	skos:exactMatch	DOID:349	systemic mastocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016587	arrhythmogenic right ventricular cardiomyopathy	skos:exactMatch	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0016596	hyperphosphatasia-intellectual disability syndrome	skos:exactMatch	DOID:0070431	hyperphosphatasia with impaired intellectual development syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0016612	X-linked cerebellar ataxia	skos:exactMatch	DOID:0050953	X-linked hereditary ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016612	X-linked cerebellar ataxia	skos:exactMatch	DOID:0111828	X-linked cerebellar ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016620	primary hypertrophic osteoarthropathy	skos:exactMatch	DOID:14283	primary hypertrophic osteoarthropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0016642	meningioma	skos:exactMatch	DOID:3565	meningioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016643	frontonasal dysplasia	skos:exactMatch	DOID:0081044	frontonasal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016648	multiple epiphyseal dysplasia	skos:exactMatch	DOID:12721	multiple epiphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016649	Warburg micro syndrome	skos:exactMatch	DOID:0060237	Warburg micro syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016660	autosomal recessive primary microcephaly	skos:exactMatch	DOID:0070296	primary autosomal recessive microcephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0016675	distal arthrogryposis type 10	skos:exactMatch	DOID:0111593	distal arthrogryposis type 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0016683	gliomatosis cerebri	skos:exactMatch	DOID:6128	gliomatosis cerebri	semapv:ManualMappingCuration	2023-03-17
MONDO:0016690	pleomorphic xanthoastrocytoma	skos:exactMatch	DOID:4852	pleomorphic xanthoastrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016691	pilocytic astrocytoma	skos:exactMatch	DOID:4851	pilocytic astrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016692	pilomyxoid astrocytoma	skos:exactMatch	DOID:4845	pilomyxoid astrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016693	subependymal giant cell astrocytoma	skos:exactMatch	DOID:5077	subependymal giant cell astrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016700	anaplastic ependymoma	skos:exactMatch	DOID:5074	high grade ependymoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016700	anaplastic ependymoma	skos:exactMatch	DOID:5889	anaplastic ependymoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016707	astroblastoma	skos:exactMatch	DOID:7305	astroblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016710	medulloblastoma with extensive nodularity	skos:exactMatch	DOID:3873	desmoplastic/nodular medulloblastoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0016715	ependymoblastoma	skos:exactMatch	DOID:0080903	embryonal tumor with multilayered rosettes, C19MC-altered	semapv:ManualMappingCuration	2023-03-17
MONDO:0016715	ependymoblastoma	skos:exactMatch	DOID:4794	ependymoblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016718	choroid plexus carcinoma	skos:exactMatch	DOID:5648	choroid plexus carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016727	extraventricular neurocytoma	skos:exactMatch	DOID:0081314	extraventricular neurocytoma	semapv:ManualMappingCuration	2023-08-20
MONDO:0016730	gangliocytoma	skos:exactMatch	DOID:2426	gangliocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016735	papillary glioneuronal tumor	skos:exactMatch	DOID:0081283	papillary glioneuronal tumor	semapv:ManualMappingCuration	2023-04-17
MONDO:0016736	rosette-forming glioneuronal tumor of fourth ventricule	skos:exactMatch	DOID:0081284	rosette-forming glioneuronal tumor	semapv:ManualMappingCuration	2023-04-17
MONDO:0016748	hemangioblastoma	skos:exactMatch	DOID:5241	hemangioblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0016757	malignant triton tumor	skos:exactMatch	DOID:6707	malignant triton tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0016759	pontocerebellar hypoplasia type 2	skos:exactMatch	DOID:0112328	pontocerebellar hypoplasia type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0016761	spondyloepiphyseal dysplasia	skos:exactMatch	DOID:0112280	spondyloepiphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016763	spondylometaphyseal dysplasia	skos:exactMatch	DOID:0112295	spondylometaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0016779	multiple congenital anomalies due to 14q32.2 maternally expressed gene defect	skos:exactMatch	DOID:0111712	Kagami-Ogata syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016817	Meier-Gorlin syndrome	skos:exactMatch	DOID:0060306	Meier-Gorlin syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0016820	Moyamoya disease	skos:exactMatch	DOID:13099	Moyamoya disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0016824	infantile myofibromatosis	skos:exactMatch	DOID:0080109	infantile myofibromatosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0016830	Emery-Dreifuss muscular dystrophy	skos:exactMatch	DOID:11726	Emery-Dreifuss muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0016955	partial duplication of the long arm of chromosome 4	skos:exactMatch	DOID:0111159	partial trisomy distal 4q	semapv:ManualMappingCuration	2023-03-17
MONDO:0016971	limb-girdle muscular dystrophy	skos:exactMatch	DOID:11724	limb-girdle muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0016974	thymoma type B	skos:exactMatch	DOID:3282	thymoma type B	semapv:ManualMappingCuration	2023-03-17
MONDO:0016987	neuroacanthocytosis	skos:exactMatch	DOID:0050765	neuroacanthocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017042	thanatophoric dysplasia	skos:exactMatch	DOID:13481	thanatophoric dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017043	congenital mesoblastic nephroma	skos:exactMatch	DOID:4773	congenital mesoblastic nephroma	semapv:ManualMappingCuration	2023-03-17
MONDO:0017093	unilateral focal polymicrogyria	skos:exactMatch	DOID:0080919	unilateral focal polymicrogyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0017123	arthrogryposis-renal dysfunction-cholestasis syndrome	skos:exactMatch	DOID:0050763	ARC syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017136	omodysplasia	skos:exactMatch	DOID:0060288	omodysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017138	Opitz G/BBB syndrome	skos:exactMatch	DOID:0050780	Opitz-GBBB syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017138	Opitz G/BBB syndrome	skos:exactMatch	DOID:0080697	Opitz GBBB syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0017169	multiple endocrine neoplasia	skos:exactMatch	DOID:3125	multiple endocrine neoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017178	osteochondritis dissecans	skos:exactMatch	DOID:84	osteochondritis dissecans	semapv:ManualMappingCuration	2023-03-17
MONDO:0017194	Blount disease	skos:exactMatch	DOID:14798	Blount's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0017195	Bruck syndrome	skos:exactMatch	DOID:0060231	Bruck syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017198	osteopetrosis	skos:exactMatch	DOID:13533	osteopetrosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017202	acute endophthalmitis	skos:exactMatch	DOID:11752	acute endophthalmitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0017203	chronic endophthalmitis	skos:exactMatch	DOID:10697	chronic endophthalmitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0017210	infectious anterior uveitis	skos:exactMatch	DOID:9389	infectious anterior uveitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0017219	microform holoprosencephaly	skos:exactMatch	DOID:0111380	solitary median maxillary central incisor	semapv:ManualMappingCuration	2023-03-17
MONDO:0017236	rapidly progressive glomerulonephritis	skos:exactMatch	DOID:4776	rapidly progressive glomerulonephritis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017265	autosomal recessive congenital ichthyosis	skos:exactMatch	DOID:0060655	autosomal recessive congenital ichthyosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017276	frontotemporal dementia	skos:exactMatch	DOID:9255	frontotemporal dementia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017278	autoimmune polyendocrinopathy	skos:exactMatch	DOID:14040	autoimmune polyendocrine syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017279	young-onset Parkinson disease	skos:exactMatch	DOID:0060894	early-onset Parkinson's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0017287	IgG4-related disease	skos:exactMatch	DOID:0080356	IgG4-related disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0017304	ocular albinism	skos:exactMatch	DOID:0050633	ocular albinism 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0017312	Perrault syndrome	skos:exactMatch	DOID:0050857	Perrault syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017319	hereditary elliptocytosis	skos:exactMatch	DOID:2373	hereditary elliptocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017324	autosomal recessive hypophosphatemic rickets	skos:exactMatch	DOID:0050949	autosomal recessive hypophosphatemic rickets	semapv:ManualMappingCuration	2023-03-17
MONDO:0017338	fatal multiple mitochondrial dysfunctions syndrome	skos:exactMatch	DOID:0070330	multiple mitochondrial dysfunctions syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017359	3-methylglutaconic aciduria	skos:exactMatch	DOID:0060336	3-methylglutaconic aciduria	semapv:ManualMappingCuration	2023-03-17
MONDO:0017386	pleomorphic rhabdomyosarcoma	skos:exactMatch	DOID:3250	pleomorphic rhabdomyosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0017387	epithelioid sarcoma	skos:exactMatch	DOID:6193	epithelioid sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0017398	3MC syndrome	skos:exactMatch	DOID:0060225	3MC syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017401	familial isolated arrhythmogenic ventricular dysplasia, left dominant form	skos:exactMatch	DOID:0070534	arrhythmogenic left ventricular cardiomyopathy	semapv:ManualMappingCuration	2024-04-21
MONDO:0017402	familial isolated arrhythmogenic ventricular dysplasia, biventricular form	skos:exactMatch	DOID:0070535	arrhythmogenic biventricular cardiomyopathy	semapv:ManualMappingCuration	2024-04-21
MONDO:0017410	porencephaly	skos:exactMatch	DOID:0060263	porencephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0017415	multiple pterygium syndrome	skos:exactMatch	DOID:0080110	contractures, pterygia, and spondylocarpotarsal fusion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017417	renal-hepatic-pancreatic dysplasia	skos:exactMatch	DOID:0060259	renal-hepatic-pancreatic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017435	popliteal pterygium syndrome	skos:exactMatch	DOID:0060055	popliteal pterygium syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017436	lethal congenital contracture syndrome	skos:exactMatch	DOID:0060558	lethal congenital contracture syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017569	de Barsy syndrome	skos:exactMatch	DOID:0070143	autosomal recessive cutis laxa type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0017570	leukocyte adhesion deficiency	skos:exactMatch	DOID:6612	leukocyte adhesion deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0017579	Baraitser-Winter cerebrofrontofacial syndrome	skos:exactMatch	DOID:0060229	Baraitser-Winter syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017582	pituitary adenocarcinoma	skos:exactMatch	DOID:4916	pituitary carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0017596	diffuse large B-cell lymphoma of the central nervous system	skos:exactMatch	DOID:0081313	primary diffuse large B-cell lymphoma of the central nervous system	semapv:ManualMappingCuration	2023-04-17
MONDO:0017607	caudal regression sequence	skos:exactMatch	DOID:0080700	caudal regression syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0017610	epidermolysis bullosa simplex	skos:exactMatch	DOID:4644	epidermolysis bullosa simplex	semapv:ManualMappingCuration	2023-03-17
MONDO:0017612	junctional epidermolysis bullosa	skos:exactMatch	DOID:3209	junctional epidermolysis bullosa	semapv:ManualMappingCuration	2023-03-17
MONDO:0017615	benign familial infantile epilepsy	skos:exactMatch	DOID:0060169	benign familial infantile epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0017623	PTEN hamartoma tumor syndrome	skos:exactMatch	DOID:0080191	PTEN hamartoma tumor syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017675	punctate palmoplantar keratoderma	skos:exactMatch	DOID:0060361	punctate palmoplantar keratoderma	semapv:ManualMappingCuration	2023-03-17
MONDO:0017719	gangliosidosis	skos:exactMatch	DOID:2368	gangliosidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017720	GM2 gangliosidosis	skos:exactMatch	DOID:3321	GM2 gangliosidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017771	Mayer-Rokitansky-Kuster-Hauser syndrome	skos:exactMatch	DOID:0112177	Mayer-Rokitansky-Kuster-Hauser syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017774	hypobetalipoproteinemia	skos:exactMatch	DOID:1390	hypobetalipoproteinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017779	alpha-N-acetylgalactosaminidase deficiency	skos:exactMatch	DOID:0112317	Schindler disease	semapv:ManualMappingCuration	2023-04-17
MONDO:0017795	ameloblastoma	skos:exactMatch	DOID:0050894	ameloblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0017810	variant ABeta2M amyloidosis	skos:exactMatch	DOID:0080929	variant ABeta2M amyloidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017813	van Maldergem syndrome	skos:exactMatch	DOID:0060238	Van Maldergem syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017814	primary bone lymphoma	skos:exactMatch	DOID:6759	bone lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0017838	sclerosteosis	skos:exactMatch	DOID:0060251	sclerosteosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017842	Senior-Loken syndrome	skos:exactMatch	DOID:0050576	Senior-Loken syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017845	spastic ataxia	skos:exactMatch	DOID:0050952	spastic ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017851	erythrokeratodermia variabilis	skos:exactMatch	DOID:0050467	erythrokeratodermia variabilis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017853	hypersensitivity pneumonitis	skos:exactMatch	DOID:841	extrinsic allergic alveolitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017886	MIT family translocation renal cell carcinoma	skos:exactMatch	DOID:0081413	renal cell carcinoma with MiT translocations	semapv:ManualMappingCuration	2024-04-21
MONDO:0017894	acute myeloid leukemia with CEBPA somatic mutations	skos:exactMatch	DOID:0081095	acute myeloid leukemia with mutated CEBPA	semapv:ManualMappingCuration	2023-04-17
MONDO:0017906	amyloidosis cutis dyschromia	skos:exactMatch	DOID:0080932	primary localized cutaneous amyloidosis 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0017909	inherited glutathione synthetase deficiency	skos:exactMatch	DOID:0080699	glutathione synthetase deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0017910	dehydrated hereditary stomatocytosis	skos:exactMatch	DOID:0111575	dehydrated hereditary stomatocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017919	exstrophy-epispadias complex	skos:exactMatch	DOID:0080173	bladder exstrophy-epispadias-cloacal exstrophy complex	semapv:ManualMappingCuration	2023-03-17
MONDO:0017923	multiple synostoses syndrome	skos:exactMatch	DOID:0050794	multiple synostoses syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017979	autoimmune lymphoproliferative syndrome	skos:exactMatch	DOID:6688	autoimmune lymphoproliferative syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0017985	congenital radioulnar synostosis	skos:exactMatch	DOID:9827	radioulnar synostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0017987	syringomyelia	skos:exactMatch	DOID:327	syringomyelia	semapv:ManualMappingCuration	2023-03-17
MONDO:0017990	catecholaminergic polymorphic ventricular tachycardia	skos:exactMatch	DOID:0060674	catecholaminergic polymorphic ventricular tachycardia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018029	congenital factor XIII deficiency	skos:exactMatch	DOID:2211	factor XIII deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0018037	hyper-IgE syndrome	skos:exactMatch	DOID:0080545	hyper IgE syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018039	selective IgM deficiency	skos:exactMatch	DOID:0050222	selective IgM deficiency disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0018053	trichothiodystrophy	skos:exactMatch	DOID:0111866	trichothiodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018054	familial atrial fibrillation	skos:exactMatch	DOID:0050650	familial atrial fibrillation	semapv:ManualMappingCuration	2023-03-17
MONDO:0018055	pediatric hepatocellular carcinoma	skos:exactMatch	DOID:0070322	childhood hepatocellular carcinoma	semapv:ManualMappingCuration	2023-11-19
MONDO:0018068	trisomy 13	skos:exactMatch	DOID:11665	Patau syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018071	trisomy 18	skos:exactMatch	DOID:1085	Edwards syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018075	neural tube defect	skos:exactMatch	DOID:0080074	neural tube defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0018076	tuberculosis	skos:exactMatch	DOID:399	tuberculosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0018088	familial Mediterranean fever	skos:exactMatch	DOID:2987	familial Mediterranean fever	semapv:ManualMappingCuration	2023-03-17
MONDO:0018089	double outlet right ventricle	skos:exactMatch	DOID:6406	double outlet right ventricle	semapv:ManualMappingCuration	2023-03-17
MONDO:0018092	Vogt-Koyanagi-Harada disease	skos:exactMatch	DOID:12297	Vogt-Koyanagi-Harada disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0018094	Waardenburg syndrome	skos:exactMatch	DOID:9258	Waardenburg syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018096	Weill-Marchesani syndrome	skos:exactMatch	DOID:0050475	Weill-Marchesani syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018097	West syndrome	skos:exactMatch	DOID:0050562	West syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018100	familial primary hypomagnesemia	skos:exactMatch	DOID:0060879	primary hypomagnesemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018102	corneal dystrophy	skos:exactMatch	DOID:2566	corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018105	Wolfram syndrome	skos:exactMatch	DOID:10632	Wolfram syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018106	hereditary xanthinuria	skos:exactMatch	DOID:0060236	xanthinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0018116	galactosemia	skos:exactMatch	DOID:9870	galactosemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018130	brain dopamine-serotonin vesicular transport disease	skos:exactMatch	DOID:0070490	infantile parkinsonism-dystonia 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0018149	GM1 gangliosidosis	skos:exactMatch	DOID:3322	GM1 gangliosidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0018150	Gaucher disease	skos:exactMatch	DOID:1926	Gaucher's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0018151	coenzyme Q10 deficiency	skos:exactMatch	DOID:0050730	coenzyme Q10 deficiency disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0018155	lateral sclerosis	skos:exactMatch	DOID:230	lateral sclerosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0018158	mitochondrial DNA depletion syndrome	skos:exactMatch	DOID:0070329	mitochondrial DNA depletion syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018159	atypical hemolytic-uremic syndrome with DGKE deficiency	skos:exactMatch	DOID:0080388	nephrotic syndrome type 7	semapv:ManualMappingCuration	2023-03-17
MONDO:0018160	hereditary retinoblastoma	skos:exactMatch	DOID:4648	familial retinoblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018163	autosomal recessive cutis laxa type 2A	skos:exactMatch	DOID:0070134	autosomal recessive cutis laxa type IIA	semapv:ManualMappingCuration	2023-03-17
MONDO:0018171	malignant germ cell tumor of ovary	skos:exactMatch	DOID:2155	malignant ovarian germ cell neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0018184	gastric linitis plastica	skos:exactMatch	DOID:4023	linitis plastica	semapv:ManualMappingCuration	2024-07-21
MONDO:0018190	autosomal dominant childhood-onset proximal spinal muscular atrophy	skos:exactMatch	DOID:0070348	spinal muscular atrophy with lower extremity predominant	semapv:ManualMappingCuration	2023-04-17
MONDO:0018213	hereditary sensory and autonomic neuropathy type 1	skos:exactMatch	DOID:0070162	hereditary sensory and autonomic neuropathy type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0018214	generalized epilepsy with febrile seizures plus	skos:exactMatch	DOID:0060170	generalized epilepsy with febrile seizures plus	semapv:ManualMappingCuration	2023-03-17
MONDO:0018216	Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome	skos:exactMatch	DOID:0050880	Koolen de Vries syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018233	otopalatodigital syndrome spectrum disorder	skos:exactMatch	DOID:0111782	otopalatodigital syndrome spectrum disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0018234	dysostosis	skos:exactMatch	DOID:1934	dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0018237	acrofacial dysostosis	skos:exactMatch	DOID:0060379	acrofacial dysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0018264	oculocutaneous albinism type 6	skos:exactMatch	DOID:0080614	oculocutaneous albinism type VI	semapv:ManualMappingCuration	2023-03-17
MONDO:0018274	GM3 synthase deficiency	skos:exactMatch	DOID:0060470	salt and pepper syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018276	muscular dystrophy-dystroglycanopathy	skos:exactMatch	DOID:0112374	muscular dystrophy-dystroglycanopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018305	chronic granulomatous disease	skos:exactMatch	DOID:3265	chronic granulomatous disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0018306	Griscelli syndrome	skos:exactMatch	DOID:0060831	Griscelli syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018307	neurodegeneration with brain iron accumulation	skos:exactMatch	DOID:0110734	neurodegeneration with brain iron accumulation	semapv:ManualMappingCuration	2023-03-17
MONDO:0018309	Hirschsprung disease	skos:exactMatch	DOID:10487	Hirschsprung's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0018319	familial episodic pain syndrome	skos:exactMatch	DOID:0111728	familial episodic pain syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018327	glomus tumor	skos:exactMatch	DOID:2431	glomus tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0018352	squamous cell carcinoma of penis	skos:exactMatch	DOID:5518	penis squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018364	malignant epithelial tumor of ovary	skos:exactMatch	DOID:2151	malignant ovarian surface epithelial-stromal neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0018369	immature ovarian teratoma	skos:exactMatch	DOID:6331	immature teratoma of ovary	semapv:ManualMappingCuration	2024-04-21
MONDO:0018458	familial hypocalciuric hypercalcemia	skos:exactMatch	DOID:0060699	familial hypocalciuric hypercalcemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018470	renal agenesis	skos:exactMatch	DOID:14766	renal agenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0018473	hyperlipoproteinemia type 3	skos:exactMatch	DOID:3145	hyperlipoproteinemia type III	semapv:ManualMappingCuration	2023-03-17
MONDO:0018477	bilirubin encephalopathy	skos:exactMatch	DOID:2382	kernicterus	semapv:ManualMappingCuration	2023-03-17
MONDO:0018479	congenital adrenal hyperplasia	skos:exactMatch	DOID:0050811	congenital adrenal hyperplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018492	hereditary clear cell renal cell carcinoma	skos:exactMatch	DOID:7192	hereditary conventional renal cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018493	malignant hyperthermia of anesthesia	skos:exactMatch	DOID:8545	malignant hyperthermia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018513	squamous cell carcinoma of colon	skos:exactMatch	DOID:5519	colon squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018515	squamous cell carcinoma of rectum	skos:exactMatch	DOID:5528	rectum squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018521	squamous cell carcinoma of pancreas	skos:exactMatch	DOID:0080323	pancreatic squamous cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018523	pancreatic mucinous cystadenoma	skos:exactMatch	DOID:7235	pancreatic mucinous cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0018523	pancreatic mucinous cystadenoma	skos:exactMatch	DOID:7735	pancreatic colloid cystadenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0018540	PFAPA syndrome	skos:exactMatch	DOID:0081451	PFAPA syndrome	semapv:ManualMappingCuration	2024-05-19
MONDO:0018542	severe congenital neutropenia	skos:exactMatch	DOID:0050590	severe congenital neutropenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018543	autosomal dominant hypocalcemia	skos:exactMatch	DOID:0090109	autosomal dominant hypocalcemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018544	adrenoleukodystrophy	skos:exactMatch	DOID:10588	adrenoleukodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018555	hypogonadotropic hypogonadism	skos:exactMatch	DOID:0090070	hypogonadotropic hypogonadism	semapv:ManualMappingCuration	2023-03-17
MONDO:0018570	hypophosphatasia	skos:exactMatch	DOID:14213	hypophosphatasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018582	GCGR-related hyperglucagonemia	skos:exactMatch	DOID:0112306	Mahvash disease	semapv:ManualMappingCuration	2023-04-17
MONDO:0018590	ABeta2M amyloidosis	skos:exactMatch	DOID:0080928	dialysis-related amyloidosis	semapv:ManualMappingCuration	2023-04-17
MONDO:0018612	congenital hypothyroidism	skos:exactMatch	DOID:0050328	congenital hypothyroidism	semapv:ManualMappingCuration	2023-03-17
MONDO:0018637	familial chylomicronemia syndrome	skos:exactMatch	DOID:0111417	familial chylomicronemia syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018638	pseudohypoaldosteronism	skos:exactMatch	DOID:4479	pseudohypoaldosteronism	semapv:ManualMappingCuration	2023-03-17
MONDO:0018661	Zika virus infectious disease	skos:exactMatch	DOID:0060478	Zika fever	semapv:ManualMappingCuration	2023-03-17
MONDO:0018677	visceral heterotaxy	skos:exactMatch	DOID:0050545	visceral heterotaxy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018696	corticobasal syndrome	skos:exactMatch	DOID:0081392	corticobasal degeneration syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0018734	verrucous hemangioma	skos:exactMatch	DOID:470	verrucous keratotic hemangioma	semapv:ManualMappingCuration	2023-11-19
MONDO:0018760	DeSanto-Shinawi syndrome	skos:exactMatch	DOID:0081126	DeSanto-Shinawi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018768	familial cold autoinflammatory syndrome	skos:exactMatch	DOID:0090061	familial cold autoinflammatory syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018770	Jeune syndrome	skos:exactMatch	DOID:0050592	asphyxiating thoracic dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018772	Joubert syndrome	skos:exactMatch	DOID:0050777	Joubert syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018778	intermediate Charcot-Marie-Tooth disease	skos:exactMatch	DOID:0050543	Charcot-Marie-Tooth disease intermediate type	semapv:ManualMappingCuration	2023-03-17
MONDO:0018800	Kallmann syndrome	skos:exactMatch	DOID:3614	Kallmann syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018801	congenital bilateral absence of vas deferens	skos:exactMatch	DOID:0111862	congenital bilateral absence of vas deferens	semapv:ManualMappingCuration	2023-03-17
MONDO:0018820	recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome	skos:exactMatch	DOID:0081386	TANGO2-related metabolic encephalopathy and arrythmias	semapv:ManualMappingCuration	2024-04-21
MONDO:0018838	lissencephaly spectrum disorders	skos:exactMatch	DOID:0050453	lissencephaly	semapv:ManualMappingCuration	2023-03-17
MONDO:0018843	embryonal carcinoma of the central nervous system	skos:exactMatch	DOID:7232	central nervous system embryonal carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018849	dentinogenesis imperfecta	skos:exactMatch	DOID:4154	dentinogenesis imperfecta	semapv:ManualMappingCuration	2023-03-17
MONDO:0018852	achromatopsia	skos:exactMatch	DOID:13911	achromatopsia	semapv:ManualMappingCuration	2023-03-17
MONDO:0018855	keratosis pilaris atrophicans	skos:exactMatch	DOID:0080751	keratosis pilaris atrophicans	semapv:ManualMappingCuration	2023-03-17
MONDO:0018865	striate palmoplantar keratoderma	skos:exactMatch	DOID:0081105	keratosis palmoplantaris striata	semapv:ManualMappingCuration	2023-04-17
MONDO:0018866	Aicardi-Goutieres syndrome	skos:exactMatch	DOID:0050629	Aicardi-Goutieres syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018868	metachromatic leukodystrophy	skos:exactMatch	DOID:10581	metachromatic leukodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018870	arterial calcification of infancy	skos:exactMatch	DOID:0050644	arterial calcification of infancy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018875	Li-Fraumeni syndrome	skos:exactMatch	DOID:0111503	Li-Fraumeni syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0018875	Li-Fraumeni syndrome	skos:exactMatch	DOID:3012	Li-Fraumeni syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018878	branchiootic syndrome	skos:exactMatch	DOID:0060232	branchiootic syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018889	hyaline body myopathy	skos:exactMatch	DOID:0111267	hyaline body myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018896	thrombotic thrombocytopenic purpura	skos:exactMatch	DOID:10772	thrombotic thrombocytopenic purpura	semapv:ManualMappingCuration	2023-03-17
MONDO:0018901	left ventricular noncompaction	skos:exactMatch	DOID:0060480	left ventricular noncompaction	semapv:ManualMappingCuration	2023-03-17
MONDO:0018906	follicular lymphoma	skos:exactMatch	DOID:0050873	follicular lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018910	oculocutaneous albinism	skos:exactMatch	DOID:0050632	oculocutaneous albinism	semapv:ManualMappingCuration	2023-03-17
MONDO:0018911	maturity-onset diabetes of the young	skos:exactMatch	DOID:0050524	maturity-onset diabetes of the young	semapv:ManualMappingCuration	2023-03-17
MONDO:0018919	McCune-Albright syndrome	skos:exactMatch	DOID:1858	McCune Albright syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018921	Meckel syndrome	skos:exactMatch	DOID:0050778	Meckel syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018931	mucolipidosis type III, alpha/beta	skos:exactMatch	DOID:0080071	mucolipidosis III alpha/beta	semapv:ManualMappingCuration	2023-03-17
MONDO:0018937	mucopolysaccharidosis type 3	skos:exactMatch	DOID:12801	mucopolysaccharidosis III	semapv:ManualMappingCuration	2023-03-17
MONDO:0018938	mucopolysaccharidosis type 4	skos:exactMatch	DOID:12804	mucopolysaccharidosis IV	semapv:ManualMappingCuration	2023-03-17
MONDO:0018940	congenital myasthenic syndrome	skos:exactMatch	DOID:3635	congenital myasthenic syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018943	myofibrillar myopathy	skos:exactMatch	DOID:0080307	myofibrillar myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018944	gestational trophoblastic neoplasm	skos:exactMatch	DOID:3590	gestational trophoblastic neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0018945	McLeod neuroacanthocytosis syndrome	skos:exactMatch	DOID:0112107	McLeod syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0018947	centronuclear myopathy	skos:exactMatch	DOID:14717	centronuclear myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018948	multiminicore myopathy	skos:exactMatch	DOID:0080991	congenital myopathy 1B	semapv:ManualMappingCuration	2023-04-17
MONDO:0018949	distal myopathy	skos:exactMatch	DOID:11720	distal myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018950	3-methylcrotonyl-CoA carboxylase deficiency	skos:exactMatch	DOID:0050710	3-methylcrotonyl-CoA carboxylase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0018953	parietal foramina	skos:exactMatch	DOID:0060285	parietal foramina	semapv:ManualMappingCuration	2023-03-17
MONDO:0018954	Loeys-Dietz syndrome	skos:exactMatch	DOID:0050466	Loeys-Dietz syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018958	nemaline myopathy	skos:exactMatch	DOID:3191	nemaline myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0018961	familial melanoma	skos:exactMatch	DOID:6846	familial melanoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0018965	Alport syndrome	skos:exactMatch	DOID:10983	Alport syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018975	neurofibromatosis type 1	skos:exactMatch	DOID:0111253	neurofibromatosis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0018983	Tolosa-Hunt syndrome	skos:exactMatch	DOID:1278	Tolosa-Hunt syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018993	Charcot-Marie-Tooth disease type 2	skos:exactMatch	DOID:0050539	Charcot-Marie-Tooth disease type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0018994	Charcot-Marie-Tooth disease type X	skos:exactMatch	DOID:0050542	Charcot-Marie-Tooth disease type X	semapv:ManualMappingCuration	2023-03-17
MONDO:0018995	Charcot-Marie-Tooth disease type 4	skos:exactMatch	DOID:0050541	Charcot-Marie-Tooth disease type 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0018996	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2	skos:exactMatch	DOID:0050755	spinocerebellar ataxia with axonal neuropathy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0018997	Noonan syndrome	skos:exactMatch	DOID:3490	Noonan syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0018998	Leber congenital amaurosis	skos:exactMatch	DOID:14791	Leber congenital amaurosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019004	kidney Wilms tumor	skos:exactMatch	DOID:2154	nephroblastoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019004	kidney Wilms tumor	skos:exactMatch	DOID:5176	renal Wilms' tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0019005	nephronophthisis	skos:exactMatch	DOID:12712	nephronophthisis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019008	benign recurrent intrahepatic cholestasis	skos:exactMatch	DOID:0070230	benign recurrent intrahepatic cholestasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019011	Charcot-Marie-Tooth disease type 1	skos:exactMatch	DOID:0050538	Charcot-Marie-Tooth disease type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0019012	Carpenter syndrome	skos:exactMatch	DOID:0060234	Carpenter syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019019	osteogenesis imperfecta	skos:exactMatch	DOID:12347	osteogenesis imperfecta	semapv:ManualMappingCuration	2023-03-17
MONDO:0019037	progressive supranuclear palsy	skos:exactMatch	DOID:678	progressive supranuclear palsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019040	chromosomal disorder	skos:exactMatch	DOID:0080014	chromosomal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019046	leukodystrophy	skos:exactMatch	DOID:0050987	hypomyelinating leukoencephalopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019046	leukodystrophy	skos:exactMatch	DOID:0060786	hypomyelinating leukodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019046	leukodystrophy	skos:exactMatch	DOID:10579	leukodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019050	inherited hemoglobinopathy	skos:exactMatch	DOID:2860	hemoglobinopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019052	inborn errors of metabolism	skos:exactMatch	DOID:655	inherited metabolic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0019053	peroxisomal disease	skos:exactMatch	DOID:906	peroxisomal disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019064	hereditary spastic paraplegia	skos:exactMatch	DOID:2476	hereditary spastic paraplegia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019071	pure hair and nail ectodermal dysplasia	skos:exactMatch	DOID:0111655	pure hair and nail ectodermal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019072	intrahepatic cholestasis	skos:exactMatch	DOID:1852	intrahepatic cholestasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019078	Ritscher-Schinzel syndrome	skos:exactMatch	DOID:0060565	Ritscher-Schinzel syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019091	bronchopulmonary dysplasia	skos:exactMatch	DOID:11650	bronchopulmonary dysplasia	semapv:ManualMappingCuration	2023-04-17
MONDO:0019107	Rh deficiency syndrome	skos:exactMatch	DOID:0050641	Rh deficiency syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019118	inherited retinal dystrophy	skos:exactMatch	DOID:8500	hereditary retinal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019118	inherited retinal dystrophy	skos:exactMatch	DOID:8501	fundus dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019142	inherited porphyria	skos:exactMatch	DOID:13268	porphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0019144	hereditary thrombophilia due to congenital protein S deficiency	skos:exactMatch	DOID:0111905	autosomal recessive thrombophilia due to protein S deficiency	semapv:ManualMappingCuration	2023-04-17
MONDO:0019145	hereditary thrombophilia due to congenital protein C deficiency	skos:exactMatch	DOID:3756	protein C deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0019148	Wolman disease	skos:exactMatch	DOID:14497	Wolman disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019149	cholesteryl ester storage disease	skos:exactMatch	DOID:14502	cholesterol ester storage disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019154	androgen insensitivity syndrome	skos:exactMatch	DOID:4674	androgen insensitivity syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019155	Leydig cell hypoplasia	skos:exactMatch	DOID:0112259	Leydig cell hypoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019169	pyruvate dehydrogenase deficiency	skos:exactMatch	DOID:3649	pyruvate decarboxylase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0019170	polyarteritis nodosa	skos:exactMatch	DOID:9810	polyarteritis nodosa	semapv:ManualMappingCuration	2023-11-19
MONDO:0019172	aniridia	skos:exactMatch	DOID:12271	aniridia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019180	hereditary hemorrhagic telangiectasia	skos:exactMatch	DOID:1270	hereditary hemorrhagic telangiectasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019181	non-syndromic X-linked intellectual disability	skos:exactMatch	DOID:0050776	non-syndromic X-linked intellectual disability	semapv:ManualMappingCuration	2023-03-17
MONDO:0019187	Axenfeld-Rieger syndrome	skos:exactMatch	DOID:14686	Axenfeld-Rieger syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019188	Rubinstein-Taybi syndrome	skos:exactMatch	DOID:1933	Rubinstein-Taybi syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019191	IgG4-related dacryoadenitis and sialadenitis	skos:exactMatch	DOID:12900	Mikulicz disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019193	acquired generalized lipodystrophy	skos:exactMatch	DOID:0080300	acquired generalized lipodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019200	retinitis pigmentosa	skos:exactMatch	DOID:10584	retinitis pigmentosa	semapv:ManualMappingCuration	2023-03-17
MONDO:0019202	myxofibrosarcoma	skos:exactMatch	DOID:0080534	myxofibrosarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019214	inborn carbohydrate metabolic disorder	skos:exactMatch	DOID:2978	carbohydrate metabolic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0019228	inborn disorder of histidine metabolism	skos:exactMatch	DOID:9265	histidine metabolism disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019234	peroxisome biogenesis disorder	skos:exactMatch	DOID:0080377	peroxisomal biogenesis disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0019238	inborn disorder of pyrimidine metabolism	skos:exactMatch	DOID:0050832	pyrimidine metabolic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0019245	lysosomal lipid storage disorder	skos:exactMatch	DOID:9455	lipid storage disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019248	mucolipidosis	skos:exactMatch	DOID:0080488	mucolipidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019249	mucopolysaccharidosis	skos:exactMatch	DOID:12798	mucopolysaccharidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019254	inborn disorder of purine or pyrimidine metabolism	skos:exactMatch	DOID:653	purine-pyrimidine metabolic disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0019255	sphingolipidosis	skos:exactMatch	DOID:1927	sphingolipidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019257	hemochromatosis type 2	skos:exactMatch	DOID:0111034	hemochromatosis type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0019264	alpha-N-acetylgalactosaminidase deficiency type 3	skos:exactMatch	DOID:0112320	Schindler disease type 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0019269	ichthyosis	skos:exactMatch	DOID:1697	ichthyosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019280	hypertrichosis	skos:exactMatch	DOID:420	hypertrichosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019284	inherited isolated nail anomaly	skos:exactMatch	DOID:0080683	nonsyndromic congenital nail disorder	semapv:ManualMappingCuration	2023-04-17
MONDO:0019287	ectodermal dysplasia syndrome	skos:exactMatch	DOID:2121	ectodermal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019288	skin pigmentation disorder	skos:exactMatch	DOID:10123	pigmentation disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019293	skin vascular disease	skos:exactMatch	DOID:9540	vascular skin disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019297	lymphedema	skos:exactMatch	DOID:4977	lymphedema	semapv:ManualMappingCuration	2023-03-17
MONDO:0019307	generalized junctional epidermolysis bullosa non-Herlitz type	skos:exactMatch	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type	semapv:ManualMappingCuration	2023-03-17
MONDO:0019312	Hermansky-Pudlak syndrome	skos:exactMatch	DOID:3753	Hermansky-Pudlak syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019313	lymphatic malformation	skos:exactMatch	DOID:0050580	hereditary lymphedema	semapv:ManualMappingCuration	2023-03-17
MONDO:0019338	sarcoidosis	skos:exactMatch	DOID:11335	sarcoidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019342	Seckel syndrome	skos:exactMatch	DOID:0050569	Seckel syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019347	peeling skin syndrome	skos:exactMatch	DOID:0060283	peeling skin syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019349	Sotos syndrome	skos:exactMatch	DOID:0112103	Sotos syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0019349	Sotos syndrome	skos:exactMatch	DOID:14748	Sotos syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019350	hereditary spherocytosis	skos:exactMatch	DOID:12971	hereditary spherocytosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019353	Stargardt disease	skos:exactMatch	DOID:0050817	Stargardt disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019354	Stickler syndrome	skos:exactMatch	DOID:0080046	Stickler syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019362	epidemic louse-borne typhus	skos:exactMatch	DOID:0050480	epidemic typhus	semapv:ManualMappingCuration	2023-03-17
MONDO:0019391	Fanconi anemia	skos:exactMatch	DOID:13636	Fanconi anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019402	beta thalassemia	skos:exactMatch	DOID:12241	beta thalassemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019403	congenital dyserythropoietic anemia	skos:exactMatch	DOID:1338	congenital dyserythropoietic anemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019404	perineurioma	skos:exactMatch	DOID:4697	perineurioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019407	microcephalic osteodysplastic dysplasia, Saul-Wilson type	skos:exactMatch	DOID:0111673	Saul-Wilson syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019409	idiopathic juvenile osteoporosis	skos:exactMatch	DOID:12559	idiopathic juvenile osteoporosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019438	AL amyloidosis	skos:exactMatch	DOID:0080933	immunoglobulin light chain amyloidosis	semapv:ManualMappingCuration	2023-04-17
MONDO:0019439	AA amyloidosis	skos:exactMatch	DOID:0080936	serum amyloid A amyloidosis	semapv:ManualMappingCuration	2023-04-17
MONDO:0019443	dextro-looped transposition of the great arteries	skos:exactMatch	DOID:0060770	dextro-looped transposition of the great arteries	semapv:ManualMappingCuration	2023-03-17
MONDO:0019465	nodal marginal zone B-cell lymphoma	skos:exactMatch	DOID:0080211	nodal marginal zone lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019469	T-cell large granular lymphocyte leukemia	skos:exactMatch	DOID:0050751	T-cell large granular lymphocyte leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019470	aggressive NK-cell leukemia	skos:exactMatch	DOID:1035	aggressive NK-cell leukemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019471	adult T-cell leukemia/lymphoma	skos:exactMatch	DOID:0050523	adult T-cell leukemia/lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019472	extranodal nasal NK/T cell lymphoma	skos:exactMatch	DOID:0080797	nasal type extranodal NK/T-cell lymphoma	semapv:ManualMappingCuration	2023-04-17
MONDO:0019474	hepatosplenic T-cell lymphoma	skos:exactMatch	DOID:0081049	hepatosplenic T-cell lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019479	histiocytic sarcoma	skos:exactMatch	DOID:0080915	histiocytic sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019490	progressive familial heart block	skos:exactMatch	DOID:0111073	progressive familial heart block	semapv:ManualMappingCuration	2023-03-17
MONDO:0019497	nonsyndromic genetic hearing loss	skos:exactMatch	DOID:0050563	nonsyndromic deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0019499	Turner syndrome	skos:exactMatch	DOID:3491	Turner syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019501	Usher syndrome	skos:exactMatch	DOID:0050439	Usher syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019502	autosomal recessive non-syndromic intellectual disability	skos:exactMatch	DOID:0060308	autosomal recessive intellectual developmental disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0019503	anterior segment dysgenesis	skos:exactMatch	DOID:0060648	anterior segment dysgenesis	semapv:ManualMappingCuration	2023-08-20
MONDO:0019507	amelogenesis imperfecta	skos:exactMatch	DOID:2187	amelogenesis imperfecta	semapv:ManualMappingCuration	2023-03-17
MONDO:0019508	van der Woude syndrome	skos:exactMatch	DOID:0060239	Van der Woude syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019514	hepatic veno-occlusive disease	skos:exactMatch	DOID:0080177	hepatic veno-occlusive disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019516	exudative vitreoretinopathy	skos:exactMatch	DOID:0050535	exudative vitreoretinopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019537	hemoglobin D disease	skos:exactMatch	DOID:5378	hemoglobin D disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019551	hereditary motor and sensory neuropathy type 6	skos:exactMatch	DOID:0080068	Charcot-Marie-Tooth disease type 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0019557	chilblain lupus	skos:exactMatch	DOID:0060386	Chilblain lupus	semapv:ManualMappingCuration	2023-03-17
MONDO:0019565	hereditary von Willebrand disease	skos:exactMatch	DOID:12531	von Willebrand's disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0019567	Ehlers-Danlos syndrome, classic type, 1	skos:exactMatch	DOID:14720	Ehlers-Danlos syndrome classic type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0019568	Ehlers-Danlos syndrome, classic type, 2	skos:exactMatch	DOID:0080726	Ehlers-Danlos syndrome classic type 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0019569	Cockayne syndrome type 1	skos:exactMatch	DOID:0080907	Cockayne syndrome A	semapv:ManualMappingCuration	2023-04-17
MONDO:0019570	Cockayne syndrome type 2	skos:exactMatch	DOID:0080908	Cockayne syndrome B	semapv:ManualMappingCuration	2023-04-17
MONDO:0019571	autosomal dominant cutis laxa	skos:exactMatch	DOID:0070142	autosomal dominant cutis laxa	semapv:ManualMappingCuration	2023-03-17
MONDO:0019572	autosomal recessive cutis laxa type 1	skos:exactMatch	DOID:0070144	autosomal recessive cutis laxa type I	semapv:ManualMappingCuration	2023-03-17
MONDO:0019586	X-linked nonsyndromic hearing loss	skos:exactMatch	DOID:0050566	X-linked nonsyndromic deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0019587	autosomal dominant nonsyndromic hearing loss	skos:exactMatch	DOID:0050564	autosomal dominant nonsyndromic deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0019588	hearing loss, autosomal recessive	skos:exactMatch	DOID:0050565	autosomal recessive nonsyndromic deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0019591	panhypopituitarism	skos:exactMatch	DOID:9410	panhypopituitarism	semapv:ManualMappingCuration	2023-03-17
MONDO:0019600	xeroderma pigmentosum	skos:exactMatch	DOID:0050427	xeroderma pigmentosum	semapv:ManualMappingCuration	2023-03-17
MONDO:0019609	Zellweger spectrum disorders	skos:exactMatch	DOID:905	Zellweger syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019623	hereditary angioedema	skos:exactMatch	DOID:14735	hereditary angioedema	semapv:ManualMappingCuration	2023-03-17
MONDO:0019624	acquired angioedema	skos:exactMatch	DOID:0080941	acquired angioedema	semapv:ManualMappingCuration	2023-03-17
MONDO:0019629	sclerocornea	skos:exactMatch	DOID:0060252	sclerocornea	semapv:ManualMappingCuration	2023-03-17
MONDO:0019631	persistent hyperplastic primary vitreous	skos:exactMatch	DOID:0060282	persistent hyperplastic primary vitreous	semapv:ManualMappingCuration	2023-03-17
MONDO:0019637	renal hypoplasia	skos:exactMatch	DOID:0080204	renal hypoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019648	achondrogenesis	skos:exactMatch	DOID:0080043	achondrogenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019666	spondyloepimetaphyseal dysplasia, PAPSS2 type	skos:exactMatch	DOID:0050812	spondyloepimetaphyseal dysplasia, Pakistani type	semapv:ManualMappingCuration	2023-03-17
MONDO:0019667	spondyloepiphyseal dysplasia tarda	skos:exactMatch	DOID:0112284	spondyloepiphyseal dysplasia tarda	semapv:ManualMappingCuration	2023-03-17
MONDO:0019669	hypochondrogenesis	skos:exactMatch	DOID:0080044	hypochondrogenesis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019675	spondyloepimetaphyseal dysplasia with joint laxity	skos:exactMatch	DOID:0112197	spondyloepimetaphyseal dysplasia with joint laxity	semapv:ManualMappingCuration	2023-03-17
MONDO:0019696	acromesomelic dysplasia	skos:exactMatch	DOID:0080049	acromesomelic dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019701	chondrodysplasia punctata	skos:exactMatch	DOID:2581	chondrodysplasia punctata	semapv:ManualMappingCuration	2023-03-17
MONDO:0019719	congenital anomaly of kidney and urinary tract	skos:exactMatch	DOID:0080205	CAKUT	semapv:ManualMappingCuration	2023-03-17
MONDO:0019771	oromandibular dystonia	skos:exactMatch	DOID:0050843	oromandibular dystonia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019772	blepharospasm-oromandibular dystonia syndrome	skos:exactMatch	DOID:3982	Meige syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019773	myelomeningocele	skos:exactMatch	DOID:0060326	myelomeningocele	semapv:ManualMappingCuration	2023-03-17
MONDO:0019796	acrocephalosyndactyly	skos:exactMatch	DOID:12960	acrocephalosyndactylia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019797	acrodysostosis	skos:exactMatch	DOID:14669	acrodysostosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019799	hepatoerythropoietic porphyria	skos:exactMatch	DOID:5230	hepatoerythropoietic porphyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0019803	angioma serpiginosum	skos:exactMatch	DOID:4028	angioma serpiginosum	semapv:ManualMappingCuration	2023-03-17
MONDO:0019804	tracheomalacia	skos:exactMatch	DOID:0060313	tracheomalacia	semapv:ManualMappingCuration	2023-03-17
MONDO:0019917	maternal uniparental disomy of chromosome 20	skos:exactMatch	DOID:0111714	Mulchandani-Bhoj-Conlin syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019930	Leydig cell hypoplasia due to complete LH resistance	skos:exactMatch	DOID:0112260	Leydig cell hypoplasia type I	semapv:ManualMappingCuration	2023-04-17
MONDO:0019931	Leydig cell hypoplasia due to partial LH resistance	skos:exactMatch	DOID:0112261	Leydig cell hypoplasia type II	semapv:ManualMappingCuration	2023-04-17
MONDO:0019941	hereditary sensory and autonomic neuropathy type 2	skos:exactMatch	DOID:0070161	hereditary sensory and autonomic neuropathy type 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0019942	distal arthrogryposis	skos:exactMatch	DOID:0050646	distal arthrogryposis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019947	rippling muscle disease 2	skos:exactMatch	DOID:0060255	rippling muscle disease 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0019948	reducing body myopathy	skos:exactMatch	DOID:0080090	reducing body myopathy 1A	semapv:ManualMappingCuration	2023-03-17
MONDO:0019950	congenital muscular dystrophy	skos:exactMatch	DOID:0050557	congenital muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019952	congenital myopathy	skos:exactMatch	DOID:0080100	congenital myopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0019952	congenital myopathy	skos:exactMatch	DOID:0081337	congenital myopathy	semapv:ManualMappingCuration	2023-07-09
MONDO:0019956	encephalitis	skos:exactMatch	DOID:9588	encephalitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0019962	thyroid lymphoma	skos:exactMatch	DOID:10011	thyroid lymphoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0019978	Robinow syndrome	skos:exactMatch	DOID:0060254	Robinow syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0019992	pseudohypoparathyroidism	skos:exactMatch	DOID:4184	pseudohypoparathyroidism	semapv:ManualMappingCuration	2023-03-17
MONDO:0020066	Ehlers-Danlos syndrome	skos:exactMatch	DOID:13359	Ehlers-Danlos syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0020068	postinfectious encephalitis	skos:exactMatch	DOID:10993	postinfectious encephalitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0020074	progressive myoclonus epilepsy	skos:exactMatch	DOID:891	progressive myoclonus epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0020088	familial partial lipodystrophy	skos:exactMatch	DOID:0050440	familial partial lipodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0020119	X-linked syndromic intellectual disability	skos:exactMatch	DOID:0060309	syndromic X-linked intellectual disability	semapv:ManualMappingCuration	2023-03-17
MONDO:0020121	muscular dystrophy	skos:exactMatch	DOID:9884	muscular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0020124	neuromuscular junction disease	skos:exactMatch	DOID:439	neuromuscular junction disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0020135	pontocerebellar hypoplasia	skos:exactMatch	DOID:0060264	pontocerebellar hypoplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0020143	cerebral lipidosis with dementia	skos:exactMatch	DOID:10742	cerebral lipidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0020153	cryptophthalmia	skos:exactMatch	DOID:0111716	cryptophthalmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0020213	stromal corneal dystrophy	skos:exactMatch	DOID:0060442	stromal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0020290	familial atrioventricular septal defect	skos:exactMatch	DOID:0050651	atrioventricular septal defect	semapv:ManualMappingCuration	2023-03-17
MONDO:0020300	autosomal dominant nocturnal frontal lobe epilepsy	skos:exactMatch	DOID:0060681	autosomal dominant nocturnal frontal lobe epilepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0020310	familial focal epilepsy with variable foci	skos:exactMatch	DOID:0081420	familial focal epilepsy with variable foci	semapv:ManualMappingCuration	2024-04-21
MONDO:0020337	congenital dyserythropoietic anemia type 1	skos:exactMatch	DOID:0111396	congenital dyserythropoietic anemia type I	semapv:ManualMappingCuration	2023-03-17
MONDO:0020340	bilateral perisylvian polymicrogyria	skos:exactMatch	DOID:0080924	bilateral perisylvian polymicrogyria	semapv:ManualMappingCuration	2023-03-17
MONDO:0020341	periventricular nodular heterotopia	skos:exactMatch	DOID:0050454	periventricular nodular heterotopia	semapv:ManualMappingCuration	2023-03-17
MONDO:0020359	congenital symblepharon	skos:exactMatch	DOID:0111720	congenital symblepharon	semapv:ManualMappingCuration	2023-03-17
MONDO:0020360	complete cryptophthalmia	skos:exactMatch	DOID:0111719	complete cryptophthalmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0020361	partial cryptophthalmia	skos:exactMatch	DOID:0111718	partial cryptophthalmia	semapv:ManualMappingCuration	2023-03-17
MONDO:0020364	posterior polymorphous corneal dystrophy	skos:exactMatch	DOID:0060457	posterior polymorphous corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0020366	congenital glaucoma	skos:exactMatch	DOID:11212	hydrophthalmos	semapv:ManualMappingCuration	2024-07-21
MONDO:0020367	juvenile open angle glaucoma	skos:exactMatch	DOID:1068	juvenile glaucoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0020369	Chandler syndrome	skos:exactMatch	DOID:11554	Chandler syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0020370	Cogan-Reese syndrome	skos:exactMatch	DOID:0060217	Cogan-Reese syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0020380	autosomal dominant cerebellar ataxia	skos:exactMatch	DOID:1441	autosomal dominant cerebellar ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0020381	patterned macular dystrophy	skos:exactMatch	DOID:0060863	patterned macular dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0020460	acquired von willebrand syndrome	skos:exactMatch	DOID:0111146	acquired von Willebrand syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0020478	Leber plus disease	skos:exactMatch	DOID:0111754	Leber plus disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0020480	sulfite oxidase deficiency due to molybdenum cofactor deficiency	skos:exactMatch	DOID:0111165	molybdenum cofactor deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0020491	subcortical band heterotopia	skos:exactMatch	DOID:0111169	subcortical band heterotopia	semapv:ManualMappingCuration	2023-03-17
MONDO:0020496	familial porencephaly	skos:exactMatch	DOID:0112313	brain small vessel disease	semapv:ManualMappingCuration	2023-06-18
MONDO:0020507	leukoencephalopathy with vanishing white matter 1	skos:exactMatch	DOID:0070374	leukoencephalopathy with vanishing white matter 1	semapv:ManualMappingCuration	2023-07-09
MONDO:0020511	precursor B-cell acute lymphoblastic leukemia	skos:exactMatch	DOID:0080638	B-cell acute lymphoblastic leukemia	semapv:ManualMappingCuration	2023-04-17
MONDO:0020513	spermatocytic seminoma	skos:exactMatch	DOID:5834	spermatocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0020513	spermatocytic seminoma	skos:exactMatch	DOID:7891	testicular spermatocytic seminoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0020525	transient neonatal diabetes mellitus	skos:exactMatch	DOID:0060334	transient neonatal diabetes mellitus	semapv:ManualMappingCuration	2023-03-17
MONDO:0020550	gestational choriocarcinoma	skos:exactMatch	DOID:2025	gestational choriocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0020603	X-linked chondrodysplasia punctata 2	skos:exactMatch	DOID:0080352	X-linked chondrodysplasia punctata 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0020604	X-linked dominant disease	skos:exactMatch	DOID:0080009	X-linked dominant disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0020605	X-linked recessive disease	skos:exactMatch	DOID:0080012	X-linked recessive disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0020630	epileptic encephalopathy, infantile or early childhood, 1	skos:exactMatch	DOID:0080472	developmental and epileptic encephalopathy 91	semapv:ManualMappingCuration	2023-03-17
MONDO:0020655	juvenile ankylosing spondylitis	skos:exactMatch	DOID:0040092	juvenile ankylosing spondylitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0020658	infiltrating ureter transitional cell carcinoma	skos:exactMatch	DOID:6845	infiltrating ureter transitional cell carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0020667	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis	skos:exactMatch	DOID:0081290	Antley-Bixler syndrome without disordered steroidogenesis	semapv:ManualMappingCuration	2024-04-21
MONDO:0020712	46,XY sex reversal 1	skos:exactMatch	DOID:0111778	46,XY sex reversal 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0020713	pulmonary venoocclusive disease 1	skos:exactMatch	DOID:0081268	pulmonary venoocclusive disease 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0020717	autosomal dominant wooly hair	skos:exactMatch	DOID:0111573	autosomal dominant woolly hair	semapv:ManualMappingCuration	2024-02-18
MONDO:0020721	X-linked sideroblastic anemia 1	skos:exactMatch	DOID:0060063	sideroblastic anemia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0020722	nephrolithiasis susceptibility caused by SLC26A1	skos:exactMatch	DOID:0080652	calcium oxalate nephrolithiasis	semapv:ManualMappingCuration	2023-06-18
MONDO:0020723	vitamin D-dependent rickets, type 1A	skos:exactMatch	DOID:0080886	vitamin D-dependent rickets type 1A	semapv:ManualMappingCuration	2023-06-18
MONDO:0020724	cerebral cavernous malformation 1	skos:exactMatch	DOID:0080491	cerebral cavernous malformation 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0020727	combined oxidative phosphorylation deficiency 22	skos:exactMatch	DOID:0111498	combined oxidative phosphorylation deficiency 22	semapv:ManualMappingCuration	2023-11-19
MONDO:0020730	carpal tunnel syndrome 1	skos:exactMatch	DOID:0070466	carpal tunnel syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0020733	proximal symphalangism 1A	skos:exactMatch	DOID:0080787	proximal symphalangism 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0020735	ACTH-independent macronodular adrenal hyperplasia 1	skos:exactMatch	DOID:0111623	ACTH-independent macronodular adrenal hyperplasia 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0020738	multiple benign circumferential skin creases on limbs 1	skos:exactMatch	DOID:0112242	congenital symmetric circumferential skin creases 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0020740	ectodermal dysplasia and immunodeficiency 1	skos:exactMatch	DOID:0081078	ectodermal dysplasia and immunodeficiency 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0020741	pyridoxine-dependent epilepsy caused by ALDH7A1 mutant	skos:exactMatch	DOID:0070519	early-onset vitamin B6-dependent epilepsy 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0020746	contractures, pterygia, and variable skeletal fusions syndrome 1B	skos:exactMatch	DOID:0081322	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B	semapv:ManualMappingCuration	2023-11-19
MONDO:0020753	Orthocoronavirinae infectious disease	skos:exactMatch	DOID:0080599	Coronavirus infectious disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0020756	migraine, familial hemiplegic, 1	skos:exactMatch	DOID:0111181	familial hemiplegic migraine 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0020772	epilepsy, juvenile absence, susceptibility to, 1	skos:exactMatch	DOID:0111324	juvenile absence epilepsy 1	semapv:ManualMappingCuration	2024-06-23
MONDO:0020820	distal arthrogryposis type 2B1	skos:exactMatch	DOID:0111600	distal arthrogryposis type 2B1	semapv:ManualMappingCuration	2023-03-17
MONDO:0020845	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5	skos:exactMatch	DOID:0111524	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0020846	intellectual disability, autosomal recessive 64	skos:exactMatch	DOID:0081225	autosomal recessive intellectual developmental disorder 64	semapv:ManualMappingCuration	2023-06-18
MONDO:0020850	intellectual disability, autosomal recessive 65	skos:exactMatch	DOID:0081226	autosomal recessive intellectual developmental disorder 65	semapv:ManualMappingCuration	2023-06-18
MONDO:0020852	spermatogenic failure 31	skos:exactMatch	DOID:0111922	spermatogenic failure 31	semapv:ManualMappingCuration	2023-03-17
MONDO:0020858	mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5	skos:exactMatch	DOID:0070463	mitochondrial complex V (ATP synthase) deficiency nuclear type 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0021002	syndactyly	skos:exactMatch	DOID:11193	syndactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0021003	polydactyly	skos:exactMatch	DOID:1148	polydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0021004	brachydactyly	skos:exactMatch	DOID:0050581	brachydactyly	semapv:ManualMappingCuration	2023-03-17
MONDO:0021005	faciodigitogenital syndrome	skos:exactMatch	DOID:0111824	Aarskog syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0021009	salivary gland mucoepidermoid carcinoma	skos:exactMatch	DOID:0081293	salivary gland mucoepidermoid carcinoma	semapv:ManualMappingCuration	2023-04-17
MONDO:0021018	autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)	skos:exactMatch	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0021022	hereditary hyperekplexia	skos:exactMatch	DOID:0060695	hyperekplexia	semapv:ManualMappingCuration	2023-03-17
MONDO:0021023	complete androgen insensitivity syndrome	skos:exactMatch	DOID:0080775	complete androgen insensitivity syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0021048	benign mastocytoma	skos:exactMatch	DOID:4658	benign mastocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0021054	bone sarcoma	skos:exactMatch	DOID:0080639	bone sarcoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0021055	classic familial adenomatous polyposis	skos:exactMatch	DOID:0050424	familial adenomatous polyposis	semapv:ManualMappingCuration	2023-03-17
MONDO:0021056	familial adenomatous polyposis 1	skos:exactMatch	DOID:0080409	familial adenomatous polyposis 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0021063	malignant colon neoplasm	skos:exactMatch	DOID:219	colon cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0021069	malignant endocrine neoplasm	skos:exactMatch	DOID:170	endocrine gland cancer	semapv:ManualMappingCuration	2023-03-17
MONDO:0021095	parkinsonian disorder	skos:exactMatch	DOID:0080855	Parkinsonism	semapv:ManualMappingCuration	2023-06-18
MONDO:0021097	intraductal breast papilloma	skos:exactMatch	DOID:1626	breast duct papilloma	semapv:ManualMappingCuration	2024-04-21
MONDO:0021107	narcolepsy	skos:exactMatch	DOID:8986	narcolepsy	semapv:ManualMappingCuration	2023-03-17
MONDO:0021115	luminal B breast carcinoma	skos:exactMatch	DOID:0080674	luminal breast carcinoma B	semapv:ManualMappingCuration	2023-04-17
MONDO:0021118	intestinal neoplasm	skos:exactMatch	DOID:4610	intestinal benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0021169	epithelioid hemangioma	skos:exactMatch	DOID:474	histiocytoid hemangioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0021259	prostate neoplasm	skos:exactMatch	DOID:13206	nodular prostate	semapv:ManualMappingCuration	2023-03-17
MONDO:0021439	benign neoplasm of pituitary gland	skos:exactMatch	DOID:60009	pituitary gland benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0021441	benign neoplasm of exocrine pancreas	skos:exactMatch	DOID:0080781	benign exocrine pancreas neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0021443	benign neoplasm of lymph node	skos:exactMatch	DOID:0080617	lymph node benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0021463	benign neoplasm of parathyroid gland	skos:exactMatch	DOID:60008	parathyroid gland benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0021503	benign neoplasm of gallbladder	skos:exactMatch	DOID:0080640	gallbladder benign neoplasm	semapv:ManualMappingCuration	2024-04-21
MONDO:0021547	amelogenesis imperfecta type 3B	skos:exactMatch	DOID:0080243	amelogenesis imperfecta type 3B	semapv:ManualMappingCuration	2023-11-19
MONDO:0021553	transverse myelitis	skos:exactMatch	DOID:0080743	transverse myelitis	semapv:ManualMappingCuration	2023-03-17
MONDO:0021569	Emery-Dreifuss muscular dystrophy 2, autosomal dominant	skos:exactMatch	DOID:0070247	autosomal dominant Emery-Dreifuss muscular dystrophy 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0021636	astrocytic tumor	skos:exactMatch	DOID:3069	malignant astrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0021637	low grade glioma	skos:exactMatch	DOID:0080829	low grade glioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0021657	ovarian sex cord-stromal tumor	skos:exactMatch	DOID:0080369	ovarian sex-cord stromal tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0022519	autoimmune myocarditis	skos:exactMatch	DOID:0080767	autoimmune myocarditis	semapv:ManualMappingCuration	2024-04-21
MONDO:0022529	BK-virus nephropathy	skos:exactMatch	DOID:0040086	polyomavirus-associated nephropathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0022687	cerebellar degeneration	skos:exactMatch	DOID:1443	cerebral degeneration	semapv:ManualMappingCuration	2023-03-17
MONDO:0022742	occupational asthma	skos:exactMatch	DOID:0080820	occupational asthma	semapv:ManualMappingCuration	2024-04-21
MONDO:0022965	desmoplastic infantile ganglioglioma	skos:exactMatch	DOID:0081259	desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0023069	enlarged vestibular aqueduct syndrome	skos:exactMatch	DOID:0050332	enlarged vestibular aqueduct	semapv:ManualMappingCuration	2023-03-17
MONDO:0023419	hyperprolinemia	skos:exactMatch	DOID:0080541	hyperprolinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0023664	spermatogenic failure 54	skos:exactMatch	DOID:0112335	spermatogenic failure 54	semapv:ManualMappingCuration	2024-08-18
MONDO:0023670	Bardet-Biedl syndrome 20	skos:exactMatch	DOID:0081009	Bardet-Biedl syndrome 20	semapv:ManualMappingCuration	2023-03-17
MONDO:0024183	wet beriberi	skos:exactMatch	DOID:0070317	wet beriberi	semapv:ManualMappingCuration	2024-04-21
MONDO:0024240	eccrine carcinoma	skos:exactMatch	DOID:4920	eccrine adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0024268	superficial mycosis	skos:exactMatch	DOID:0050133	superficial mycosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0024286	benign blood vessel neoplasm	skos:exactMatch	DOID:60006	benign vascular tumor	semapv:ManualMappingCuration	2023-04-17
MONDO:0024299	vitamin D-dependent rickets	skos:exactMatch	DOID:0080883	vitamin D-dependent rickets	semapv:ManualMappingCuration	2023-03-17
MONDO:0024301	acquired mineral metabolism disease	skos:exactMatch	DOID:0050032	mineral metabolism disease	semapv:ManualMappingCuration	2023-03-17
MONDO:0024305	acquired hyperprolactinemia	skos:exactMatch	DOID:12700	hyperprolactinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0024306	acquired lactic acidosis	skos:exactMatch	DOID:3650	lactic acidosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0024336	vulvar adenocarcinoma	skos:exactMatch	DOID:2098	vulva adenocarcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0024358	complex sleep apnea	skos:exactMatch	DOID:0080302	mixed sleep apnea	semapv:ManualMappingCuration	2023-03-17
MONDO:0024387	benign ovarian sex cord-stromal tumor	skos:exactMatch	DOID:0080370	ovarian sex cord-stromal benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0024457	neurodegeneration with brain iron accumulation 2A	skos:exactMatch	DOID:0110735	neurodegeneration with brain iron accumulation 2A	semapv:ManualMappingCuration	2023-03-17
MONDO:0024477	liver and intrahepatic bile duct neoplasm	skos:exactMatch	DOID:916	liver benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0024522	amyloidosis, primary localized cutaneous, 1	skos:exactMatch	DOID:0080930	primary localized cutaneous amyloidosis 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0024525	Fanconi renotubular syndrome 1	skos:exactMatch	DOID:0080757	Fanconi renotubular syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0024528	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1	skos:exactMatch	DOID:0111521	autosomal dominant progressive external ophthalmoplegia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0024537	Brown-Vialetto-van Laere syndrome 1	skos:exactMatch	DOID:0080785	Brown-Vialetto-Van Laere syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0024545	Miyoshi muscular dystrophy 1	skos:exactMatch	DOID:0070199	Miyoshi muscular dystrophy 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0024548	peeling skin syndrome 1	skos:exactMatch	DOID:0070520	peeling skin syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0024550	frontometaphyseal dysplasia 1	skos:exactMatch	DOID:0111786	frontometaphyseal dysplasia 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0024568	infantile liver failure syndrome 1	skos:exactMatch	DOID:0080717	infantile liver failure syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0024573	familial hypertrophic cardiomyopathy	skos:exactMatch	DOID:0080326	familial hypertrophic cardiomyopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0024622	thyroid gland adenocarcinoma	skos:exactMatch	DOID:0080524	thyroid gland adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0024647	urolithiasis	skos:exactMatch	DOID:0080653	urolithiasis	semapv:ManualMappingCuration	2023-03-17
MONDO:0024677	pancreatic insulinoma	skos:exactMatch	DOID:3892	insulinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0024686	tenosynovial giant cell tumor, diffuse type	skos:exactMatch	DOID:2702	pigmented villonodular synovitis	semapv:ManualMappingCuration	2023-11-19
MONDO:0024686	tenosynovial giant cell tumor, diffuse type	skos:exactMatch	DOID:9898	villonodular synovitis	semapv:ManualMappingCuration	2023-11-19
MONDO:0024772	intellectual developmental disorder, X-linked, syndromic, Pilorge type	skos:exactMatch	DOID:0070422	syndromic X-linked intellectual disability Pilorge type	semapv:ManualMappingCuration	2023-11-19
MONDO:0024889	benign mesonephroma	skos:exactMatch	DOID:2616	Wolffian duct adenoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0024892	soft tissue amyloid neoplasm	skos:exactMatch	DOID:6755	amyloid tumor	semapv:ManualMappingCuration	2023-03-17
MONDO:0024988	sex cord-stromal benign neoplasm	skos:exactMatch	DOID:0080368	sex cord-stromal benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0025193	oculopharyngodistal myopathy	skos:exactMatch	DOID:0081296	oculopharyngodistal myopathy	semapv:ManualMappingCuration	2023-04-17
MONDO:0025353	developmental and epileptic encephalopathy, 90	skos:exactMatch	DOID:0070381	developmental and epileptic encephalopathy 90	semapv:ManualMappingCuration	2023-11-19
MONDO:0025354	spermatogenic failure, X-linked, 3	skos:exactMatch	DOID:0112274	X-linked spermatogenic failure 3	semapv:ManualMappingCuration	2023-04-17
MONDO:0025598	pneumonia caused by chlamydia	skos:exactMatch	DOID:0040083	Chlamydia pneumonia	semapv:ManualMappingCuration	2024-04-21
MONDO:0025699	Coffin-Siris syndrome 12	skos:exactMatch	DOID:0112370	Coffin-Siris syndrome 12	semapv:ManualMappingCuration	2023-11-19
MONDO:0025701	leukodystrophy, hypomyelinating, 22	skos:exactMatch	DOID:0070402	hypomyelinating leukodystrophy 22	semapv:ManualMappingCuration	2024-06-23
MONDO:0026722	Mullegama-Klein-Martinez syndrome	skos:exactMatch	DOID:0111845	Mullegama-Klein-Martinez syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0026730	Basilicata-Akhtar syndrome	skos:exactMatch	DOID:0111838	Basilicata-Akhtar syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0026767	immunodeficiency 74, COVID-19-related, X-linked	skos:exactMatch	DOID:0112063	X-Linked immunodeficiency 74	semapv:ManualMappingCuration	2023-04-17
MONDO:0026777	VEXAS syndrome	skos:exactMatch	DOID:0080828	VEXAS syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0027069	mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1	skos:exactMatch	DOID:0111748	mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0027353	autosomal recessive dyskeratosis congenita 4	skos:exactMatch	DOID:0070021	autosomal recessive dyskeratosis congenita 4	semapv:ManualMappingCuration	2023-11-19
MONDO:0027407	Kleefstra syndrome 1	skos:exactMatch	DOID:0060352	Kleefstra syndrome 1	semapv:ManualMappingCuration	2023-08-20
MONDO:0027766	generalized lipodystrophy	skos:exactMatch	DOID:0080298	complete generalized lipodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0027767	partial lipodystrophy	skos:exactMatch	DOID:0080299	partial lipodystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0027772	lung colloid adenocarcinoma	skos:exactMatch	DOID:0080303	mucinous lung adenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0027772	lung colloid adenocarcinoma	skos:exactMatch	DOID:0080304	lung mucinous cystadenocarcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0029134	severe combined immunodeficiency due to CARMIL2 deficiency	skos:exactMatch	DOID:0111984	immunodeficiency 58	semapv:ManualMappingCuration	2023-04-17
MONDO:0029135	muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8	skos:exactMatch	DOID:0112382	muscular dystrophy-dystroglycanopathy type C8	semapv:ManualMappingCuration	2023-04-17
MONDO:0029137	hearing loss, autosomal dominant 74	skos:exactMatch	DOID:0112165	autosomal dominant nonsyndromic deafness 74	semapv:ManualMappingCuration	2023-06-18
MONDO:0029140	glycosylphosphatidylinositol biosynthesis defect 18	skos:exactMatch	DOID:0070382	developmental and epileptic encephalopathy 95	semapv:ManualMappingCuration	2023-07-09
MONDO:0029145	orofacial cleft 8	skos:exactMatch	DOID:0080401	orofacial cleft 8	semapv:ManualMappingCuration	2023-11-19
MONDO:0030006	combined oxidative phosphorylation deficiency 40	skos:exactMatch	DOID:0112117	combined oxidative phosphorylation deficiency 40	semapv:ManualMappingCuration	2023-03-17
MONDO:0030007	combined oxidative phosphorylation deficiency 41	skos:exactMatch	DOID:0112119	combined oxidative phosphorylation deficiency 41	semapv:ManualMappingCuration	2023-03-17
MONDO:0030008	combined oxidative phosphorylation deficiency 42	skos:exactMatch	DOID:0112118	combined oxidative phosphorylation deficiency 42	semapv:ManualMappingCuration	2023-03-17
MONDO:0030013	immunodeficiency 66	skos:exactMatch	DOID:0111998	immunodeficiency 66	semapv:ManualMappingCuration	2023-03-17
MONDO:0030017	combined oxidative phosphorylation deficiency 43	skos:exactMatch	DOID:0112116	combined oxidative phosphorylation deficiency 43	semapv:ManualMappingCuration	2023-03-17
MONDO:0030019	anauxetic dysplasia 3	skos:exactMatch	DOID:0080963	anauxetic dysplasia 3	semapv:ManualMappingCuration	2023-03-17
MONDO:0030020	combined oxidative phosphorylation deficiency 44	skos:exactMatch	DOID:0070424	combined oxidative phosphorylation deficiency 44	semapv:ManualMappingCuration	2024-04-21
MONDO:0030027	tremor, hereditary essential, 6	skos:exactMatch	DOID:0081295	essential tremor 6	semapv:ManualMappingCuration	2023-06-18
MONDO:0030031	lissencephaly 10	skos:exactMatch	DOID:0112229	lissencephaly 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0030049	46,xx sex reversal 5	skos:exactMatch	DOID:0080943	46,XX sex reversal 5	semapv:ManualMappingCuration	2023-03-17
MONDO:0030051	intellectual developmental disorder with autistic features and language delay, with or without seizures	skos:exactMatch	DOID:0081430	intellectual developmental disorder with autistic features and language delay, with or without seizures	semapv:ManualMappingCuration	2024-04-21
MONDO:0030054	developmental and epileptic encephalopathy, 86	skos:exactMatch	DOID:0112220	developmental and epileptic encephalopathy 86	semapv:ManualMappingCuration	2023-04-17
MONDO:0030055	neuronopathy, distal hereditary motor, autosomal recessive 8	skos:exactMatch	DOID:0081427	autosomal recessive distal hereditary motor neuronopathy 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0030058	hearing loss, autosomal dominant 77	skos:exactMatch	DOID:0112168	autosomal dominant nonsyndromic deafness 77	semapv:ManualMappingCuration	2023-06-18
MONDO:0030059	developmental and epileptic encephalopathy, 87	skos:exactMatch	DOID:0112221	developmental and epileptic encephalopathy 87	semapv:ManualMappingCuration	2023-04-17
MONDO:0030062	arrhythmogenic right ventricular dysplasia, familial, 14	skos:exactMatch	DOID:0080959	arrhythmogenic right ventricular dysplasia 14	semapv:ManualMappingCuration	2023-04-17
MONDO:0030064	episodic ataxia, type 9	skos:exactMatch	DOID:0060965	episodic ataxia type 9	semapv:ManualMappingCuration	2024-07-21
MONDO:0030065	agenesis of corpus callosum, cardiac, ocular, and genital syndrome	skos:exactMatch	DOID:0080948	agenesis of corpus callosum, cardiac, ocular, and genital syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0030066	granulomatous disease, chronic, autosomal recessive, 5	skos:exactMatch	DOID:0070368	autosomal recessive chronic granulomatous disease 5	semapv:ManualMappingCuration	2023-06-18
MONDO:0030067	Treacher Collins syndrome 4	skos:exactMatch	DOID:0080792	Treacher Collins syndrome 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0030071	retinitis pigmentosa 89	skos:exactMatch	DOID:0112146	retinitis pigmentosa 89	semapv:ManualMappingCuration	2023-03-17
MONDO:0030072	developmental and epileptic encephalopathy, 88	skos:exactMatch	DOID:0112222	developmental and epileptic encephalopathy 88	semapv:ManualMappingCuration	2023-04-17
MONDO:0030073	Mitchell syndrome	skos:exactMatch	DOID:0070516	Mitchell syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0030074	spondylometaphyseal dysplasia with corneal dystrophy	skos:exactMatch	DOID:0112303	spondylometaphyseal dysplasia with corneal dystrophy	semapv:ManualMappingCuration	2023-03-17
MONDO:0030105	galactosemia 4	skos:exactMatch	DOID:0060969	galactosemia 4	semapv:ManualMappingCuration	2024-07-21
MONDO:0030134	oculopharyngodistal myopathy 2	skos:exactMatch	DOID:0081298	oculopharyngodistal myopathy 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0030258	pontocerebellar hypoplasia, type 14	skos:exactMatch	DOID:0112325	pontocerebellar hypoplasia type 14	semapv:ManualMappingCuration	2023-11-19
MONDO:0030260	pontocerebellar hypoplasia, type 1E	skos:exactMatch	DOID:0112330	pontocerebellar hypoplasia type 1E	semapv:ManualMappingCuration	2023-06-18
MONDO:0030261	pontocerebellar hypoplasia, type 1F	skos:exactMatch	DOID:0112331	pontocerebellar hypoplasia type 1F	semapv:ManualMappingCuration	2023-11-19
MONDO:0030307	spermatogenic failure 55	skos:exactMatch	DOID:0112337	spermatogenic failure 55	semapv:ManualMappingCuration	2024-06-23
MONDO:0030318	spinocerebellar ataxia, autosomal recessive 30	skos:exactMatch	DOID:0070411	autosomal recessive spinocerebellar ataxia 30	semapv:ManualMappingCuration	2024-06-23
MONDO:0030323	spinocerebellar ataxia, autosomal recessive 31	skos:exactMatch	DOID:0070412	autosomal recessive spinocerebellar ataxia 31	semapv:ManualMappingCuration	2024-08-18
MONDO:0030326	mitochondrial dna depletion syndrome 16B (neuroophthalmic type)	skos:exactMatch	DOID:0070447	mitochondrial DNA depletion syndrome 16B	semapv:ManualMappingCuration	2024-04-21
MONDO:0030355	facioscapulohumeral muscular dystrophy 4, digenic	skos:exactMatch	DOID:0060918	facioscapulohumeral muscular dystrophy 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0030430	spermatogenic failure 56	skos:exactMatch	DOID:0112336	spermatogenic failure 56	semapv:ManualMappingCuration	2024-06-23
MONDO:0030438	pontocerebellar hypoplasia, type 16	skos:exactMatch	DOID:0112333	pontocerebellar hypoplasia type 16	semapv:ManualMappingCuration	2024-08-18
MONDO:0030453	developmental and epileptic encephalopathy 97	skos:exactMatch	DOID:0070383	developmental and epileptic encephalopathy 97	semapv:ManualMappingCuration	2024-08-18
MONDO:0030455	dystonia 31	skos:exactMatch	DOID:0060938	dystonia 31	semapv:ManualMappingCuration	2024-08-18
MONDO:0030463	spermatogenic failure 58	skos:exactMatch	DOID:0112352	spermatogenic failure 58	semapv:ManualMappingCuration	2024-08-18
MONDO:0030472	developmental and epileptic encephalopathy 98	skos:exactMatch	DOID:0070384	developmental and epileptic encephalopathy 98	semapv:ManualMappingCuration	2023-07-09
MONDO:0030473	developmental and epileptic encephalopathy 99	skos:exactMatch	DOID:0070385	developmental and epileptic encephalopathy 99	semapv:ManualMappingCuration	2023-09-24
MONDO:0030492	spermatogenic failure 59	skos:exactMatch	DOID:0112357	spermatogenic failure 59	semapv:ManualMappingCuration	2024-06-23
MONDO:0030500	Loeys-Dietz syndrome 6	skos:exactMatch	DOID:0060964	Loeys-Dietz syndrome 6	semapv:ManualMappingCuration	2024-07-21
MONDO:0030507	spermatogenic failure 61	skos:exactMatch	DOID:0112350	spermatogenic failure 61	semapv:ManualMappingCuration	2023-11-19
MONDO:0030512	spastic paraplegia 85, autosomal recessive	skos:exactMatch	DOID:0112345	hereditary spastic paraplegia 85	semapv:ManualMappingCuration	2023-11-19
MONDO:0030513	dystonia 33	skos:exactMatch	DOID:0060940	dystonia 33	semapv:ManualMappingCuration	2024-06-23
MONDO:0030514	leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy	skos:exactMatch	DOID:0070397	hypomyelinating leukodystrophy 23	semapv:ManualMappingCuration	2023-11-19
MONDO:0030515	spermatogenic failure 63	skos:exactMatch	DOID:0112356	spermatogenic failure 63	semapv:ManualMappingCuration	2023-11-19
MONDO:0030522	spermatogenic failure 64	skos:exactMatch	DOID:0112353	spermatogenic failure 64	semapv:ManualMappingCuration	2024-06-23
MONDO:0030529	agammaglobulinemia 10, autosomal dominant	skos:exactMatch	DOID:0081142	agammaglobulinemia 10	semapv:ManualMappingCuration	2023-11-19
MONDO:0030531	spermatogenic failure 65	skos:exactMatch	DOID:0112354	spermatogenic failure 65	semapv:ManualMappingCuration	2023-11-19
MONDO:0030543	combined oxidative phosphorylation deficiency 54	skos:exactMatch	DOID:0070427	combined oxidative phosphorylation deficiency 54	semapv:ManualMappingCuration	2024-04-21
MONDO:0030602	Klebsiella pneumonia	skos:exactMatch	DOID:13272	Klebsiella pneumonia	semapv:ManualMappingCuration	2024-04-21
MONDO:0030639	Teebi hypertelorism syndrome	skos:exactMatch	DOID:0081073	Teebi hypertelorism syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0030674	Teebi hypertelorism syndrome 2	skos:exactMatch	DOID:0081074	Teebi hypertelorism syndrome 2	semapv:ManualMappingCuration	2024-08-18
MONDO:0030680	cardiomyopathy, dilated, 2F	skos:exactMatch	DOID:0081162	dilated cardiomyopathy 2F	semapv:ManualMappingCuration	2023-11-19
MONDO:0030695	developmental and epileptic encephalopathy 100	skos:exactMatch	DOID:0070386	developmental and epileptic encephalopathy 100	semapv:ManualMappingCuration	2023-11-19
MONDO:0030700	autoimmune glomerulonephritis	skos:exactMatch	DOID:0040094	autoimmune glomerulonephritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0030701	autoimmune cardiomyopathy	skos:exactMatch	DOID:0040095	autoimmune cardiomyopathy	semapv:ManualMappingCuration	2024-04-21
MONDO:0030702	autoimmune atherosclerosis	skos:exactMatch	DOID:0040096	autoimmune atherosclerosis	semapv:ManualMappingCuration	2024-04-21
MONDO:0030703	autoimmune vasculitis	skos:exactMatch	DOID:0040097	autoimmune vasculitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0030727	developmental and epileptic encephalopathy 101	skos:exactMatch	DOID:0070387	developmental and epileptic encephalopathy 101	semapv:ManualMappingCuration	2023-11-19
MONDO:0030781	restrictive dermopathy 2	skos:exactMatch	DOID:0070370	restrictive dermopathy 2	semapv:ManualMappingCuration	2023-05-21
MONDO:0030785	intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly	skos:exactMatch	DOID:0081234	autosomal recessive intellectual developmental disorder 75	semapv:ManualMappingCuration	2023-11-19
MONDO:0030844	spermatogenic failure 47	skos:exactMatch	DOID:0112175	spermatogenic failure 47	semapv:ManualMappingCuration	2023-03-17
MONDO:0030846	spermatogenic failure 48	skos:exactMatch	DOID:0112176	spermatogenic failure 48	semapv:ManualMappingCuration	2023-03-17
MONDO:0030847	arthrogryposis, distal, type 1C	skos:exactMatch	DOID:0112190	distal arthrogryposis type 1C	semapv:ManualMappingCuration	2023-06-18
MONDO:0030856	developmental and epileptic encephalopathy 89	skos:exactMatch	DOID:0112223	developmental and epileptic encephalopathy 89	semapv:ManualMappingCuration	2023-11-19
MONDO:0030860	neuronopathy, distal hereditary motor, type 5C	skos:exactMatch	DOID:0081401	autosomal dominant distal hereditary motor neuronopathy 13	semapv:ManualMappingCuration	2024-04-21
MONDO:0030861	osteogenesis imperfecta, type 21	skos:exactMatch	DOID:0112201	osteogenesis imperfecta type 21	semapv:ManualMappingCuration	2023-04-17
MONDO:0030866	neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities	skos:exactMatch	DOID:0070543	neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities	semapv:ManualMappingCuration	2024-07-21
MONDO:0030868	spermatogenic failure 49	skos:exactMatch	DOID:0112271	spermatogenic failure 49	semapv:ManualMappingCuration	2023-03-17
MONDO:0030869	spermatogenic failures 50	skos:exactMatch	DOID:0112272	spermatogenic failure 50	semapv:ManualMappingCuration	2023-06-18
MONDO:0030871	vertebral hypersegmentation and orofacial anomalies	skos:exactMatch	DOID:0070418	vertebral hypersegmentation and orofacial anomalies	semapv:ManualMappingCuration	2023-11-19
MONDO:0030885	amyotrophic lateral sclerosis 26 with or without frontotemporal dementia	skos:exactMatch	DOID:0081380	amyotrophic lateral sclerosis type 26	semapv:ManualMappingCuration	2024-06-23
MONDO:0030887	cardiomyopathy, dilated, 2G	skos:exactMatch	DOID:0081163	dilated cardiomyopathy 2G	semapv:ManualMappingCuration	2023-11-19
MONDO:0030894	AMED syndrome, digenic	skos:exactMatch	DOID:0080952	AMED syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0030895	nephrotic syndrome, type 22	skos:exactMatch	DOID:0112268	nephrotic syndrome type 22	semapv:ManualMappingCuration	2023-11-19
MONDO:0030907	intellectual disability, X-linked 106	skos:exactMatch	DOID:0080240	non-syndromic X-linked intellectual disability 106	semapv:ManualMappingCuration	2023-03-17
MONDO:0030908	intellectual disability, X-linked, syndromic, 35	skos:exactMatch	DOID:0080241	syndromic X-linked intellectual disability 35	semapv:ManualMappingCuration	2023-03-17
MONDO:0030910	intellectual disability, autosomal dominant 45	skos:exactMatch	DOID:0080236	autosomal dominant intellectual developmental disorder 45	semapv:ManualMappingCuration	2023-03-17
MONDO:0030912	intellectual disability, autosomal dominant 47	skos:exactMatch	DOID:0080238	autosomal dominant intellectual developmental disorder 47	semapv:ManualMappingCuration	2023-03-17
MONDO:0030914	Clark-Baraitser syndrome	skos:exactMatch	DOID:0080234	Clark-Baraitser syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0030916	intellectual disability, autosomal dominant 50	skos:exactMatch	DOID:0080233	autosomal dominant intellectual developmental disorder 50	semapv:ManualMappingCuration	2023-03-17
MONDO:0030917	intellectual disability, autosomal dominant 51	skos:exactMatch	DOID:0080232	autosomal dominant intellectual developmental disorder 51	semapv:ManualMappingCuration	2023-03-17
MONDO:0030922	intellectual disability, autosomal dominant 56	skos:exactMatch	DOID:0080226	autosomal dominant intellectual developmental disorder 56	semapv:ManualMappingCuration	2023-03-17
MONDO:0030924	proteasome-associated autoinflammatory syndrome 5	skos:exactMatch	DOID:0060919	proteosome-associated autoinflammatory syndrome 5	semapv:ManualMappingCuration	2024-04-21
MONDO:0030926	spermatogenic failure 51	skos:exactMatch	DOID:0112273	spermatogenic failure 51	semapv:ManualMappingCuration	2023-03-17
MONDO:0030927	myofibrillar myopathy 11	skos:exactMatch	DOID:0081338	myofibrillar myopathy 11	semapv:ManualMappingCuration	2023-11-19
MONDO:0030931	proteasome-associated autoinflammatory syndrome 4	skos:exactMatch	DOID:0060915	proteosome-associated autoinflammatory syndrome 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0030938	spermatogenic failure 52	skos:exactMatch	DOID:0112270	spermatogenic failure 52	semapv:ManualMappingCuration	2023-03-17
MONDO:0030939	premature ovarian failure 18	skos:exactMatch	DOID:0112269	primary ovarian insufficiency 18	semapv:ManualMappingCuration	2023-11-19
MONDO:0030953	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2	skos:exactMatch	DOID:0112358	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2	semapv:ManualMappingCuration	2023-11-19
MONDO:0030957	developmental and epileptic encephalopathy 103	skos:exactMatch	DOID:0070389	developmental and epileptic encephalopathy 103	semapv:ManualMappingCuration	2023-11-19
MONDO:0030977	neuronopathy, distal hereditary motor, autosomal recessive 7	skos:exactMatch	DOID:0081426	autosomal recessive distal hereditary motor neuronopathy 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0030981	immunodeficiency 79	skos:exactMatch	DOID:0112277	immunodeficiency 79	semapv:ManualMappingCuration	2023-03-17
MONDO:0030985	premature ovarian failure 19	skos:exactMatch	DOID:0112278	primary ovarian insufficiency 19	semapv:ManualMappingCuration	2023-11-19
MONDO:0030989	spermatogenic failure 53	skos:exactMatch	DOID:0112279	spermatogenic failure 53	semapv:ManualMappingCuration	2024-06-23
MONDO:0031007	spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis	skos:exactMatch	DOID:0112290	spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis	semapv:ManualMappingCuration	2023-11-19
MONDO:0031012	autoimmune uveitis	skos:exactMatch	DOID:0040088	autoimmune uveitis	semapv:ManualMappingCuration	2024-04-21
MONDO:0031013	autoimmune optic neuritis	skos:exactMatch	DOID:0040089	autoimmune optic neuritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0031014	autoimmune gastritis	skos:exactMatch	DOID:0040090	autoimmune gastritis	semapv:ManualMappingCuration	2024-04-21
MONDO:0031021	developmental and epileptic encephalopathy 104	skos:exactMatch	DOID:0070390	developmental and epileptic encephalopathy 104	semapv:ManualMappingCuration	2023-11-19
MONDO:0031028	developmental and epileptic encephalopathy 105 with hypopituitarism	skos:exactMatch	DOID:0070391	developmental and epileptic encephalopathy 105	semapv:ManualMappingCuration	2023-11-19
MONDO:0031043	lymphatic malformation 12	skos:exactMatch	DOID:0081030	central conducting lymphatic anomaly	semapv:ManualMappingCuration	2024-06-23
MONDO:0031052	developmental and epileptic encephalopathy 106	skos:exactMatch	DOID:0070392	developmental and epileptic encephalopathy 106	semapv:ManualMappingCuration	2023-11-19
MONDO:0031084	amelogenesis imperfecta, IIa 1K	skos:exactMatch	DOID:0060945	amelogenesis imperfecta type 1K	semapv:ManualMappingCuration	2024-05-19
MONDO:0031166	macular dystrophy, retinal	skos:exactMatch	DOID:0070438	retinal macular dystrophy	semapv:ManualMappingCuration	2024-04-21
MONDO:0031213	restrictive dermopathy	skos:exactMatch	DOID:0060762	restrictive dermopathy	semapv:ManualMappingCuration	2023-08-20
MONDO:0031219	mismatch repair cancer syndrome	skos:exactMatch	DOID:0112182	mismatch repair cancer syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0031329	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome	skos:exactMatch	DOID:0081072	craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0031332	Glanzmann thrombasthenia 1	skos:exactMatch	DOID:2219	Glanzmann's thrombasthenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0031421	Olmsted syndrome	skos:exactMatch	DOID:0112011	mutilating palmoplantar keratoderma with periorificial keratotic plaques	semapv:ManualMappingCuration	2023-04-17
MONDO:0031632	developmental delay with short stature, dysmorphic facial features, and sparse hair	skos:exactMatch	DOID:0070476	diphthamide deficiency syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0032607	vertebral anomalies and variable endocrine and T-cell dysfunction	skos:exactMatch	DOID:0070345	vertebral anomalies and variable endocrine and T-cell dysfunction	semapv:ManualMappingCuration	2023-11-19
MONDO:0032610	mitochondrial complex 1 deficiency, nuclear type 5	skos:exactMatch	DOID:0112068	nuclear type mitochondrial complex I deficiency 5	semapv:ManualMappingCuration	2023-06-18
MONDO:0032631	mitochondrial complex 1 deficiency, nuclear type 27	skos:exactMatch	DOID:0112090	nuclear type mitochondrial complex I deficiency 27	semapv:ManualMappingCuration	2024-04-21
MONDO:0032637	ciliary dyskinesia, primary, 39	skos:exactMatch	DOID:0111854	primary ciliary dyskinesia 39	semapv:ManualMappingCuration	2023-06-18
MONDO:0032648	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations	skos:exactMatch	DOID:0111403	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations	semapv:ManualMappingCuration	2023-11-19
MONDO:0032655	visual impairment and progressive phthisis bulbi	skos:exactMatch	DOID:0070356	visual impairment and progressive phthisis bulbi	semapv:ManualMappingCuration	2023-11-19
MONDO:0032664	ciliary dyskinesia, primary, 40	skos:exactMatch	DOID:0111853	primary ciliary dyskinesia 40	semapv:ManualMappingCuration	2023-06-18
MONDO:0032677	lissencephaly 9 with complex brainstem malformation	skos:exactMatch	DOID:0112228	lissencephaly 9 with complex brainstem malformation	semapv:ManualMappingCuration	2023-03-17
MONDO:0032687	intellectual developmental disorder with abnormal behavior, microcephaly, and short stature	skos:exactMatch	DOID:0081265	intellectual developmental disorder with abnormal behavior, microcephaly, and short stature	semapv:ManualMappingCuration	2023-04-17
MONDO:0032690	microcephaly, growth deficiency, seizures, and brain malformations	skos:exactMatch	DOID:0081051	microcephaly, growth deficiency, seizures, and brain malformations	semapv:ManualMappingCuration	2023-11-19
MONDO:0032728	Charcot-Marie-Tooth disease, axonal, type 2EE	skos:exactMatch	DOID:0111559	Charcot-Marie-Tooth disease type 2EE	semapv:ManualMappingCuration	2023-04-17
MONDO:0032737	spastic paraplegia 80, autosomal dominant	skos:exactMatch	DOID:0112341	hereditary spastic paraplegia 80	semapv:ManualMappingCuration	2023-06-18
MONDO:0032751	arthrogryposis, distal, type 2B3	skos:exactMatch	DOID:0111602	distal arthrogryposis type 2B3	semapv:ManualMappingCuration	2023-03-17
MONDO:0032763	immunodeficiency 62	skos:exactMatch	DOID:0111991	immunodeficiency 62	semapv:ManualMappingCuration	2023-03-17
MONDO:0032766	hypoalphalipoproteinemia, primary, 2	skos:exactMatch	DOID:0080958	primary hypoalphalipoproteinemia 2	semapv:ManualMappingCuration	2023-11-19
MONDO:0032778	arthrogryposis multiplex congenita 3, myogenic type	skos:exactMatch	DOID:0080979	arthrogryposis multiplex congenita-3	semapv:ManualMappingCuration	2024-04-21
MONDO:0032787	holoprosencephaly 12 with or without pancreatic agenesis	skos:exactMatch	DOID:0081398	holoprosencephaly 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0032790	neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities	skos:exactMatch	DOID:0081443	Stolerman neurodevelopmental syndrome	semapv:ManualMappingCuration	2024-05-19
MONDO:0032799	mitochondrial DNA depletion syndrome 16 (hepatic type)	skos:exactMatch	DOID:0070446	mitochondrial DNA depletion syndrome 16	semapv:ManualMappingCuration	2024-04-21
MONDO:0032819	hypothyroidism, congenital, nongoitrous, 7	skos:exactMatch	DOID:0111836	congenital nongoitrous hypothyroidism 7	semapv:ManualMappingCuration	2023-11-19
MONDO:0032837	abdominal obesity-metabolic syndrome 4	skos:exactMatch	DOID:0080945	abdominal obesity-metabolic syndrome 4	semapv:ManualMappingCuration	2023-11-19
MONDO:0032845	spermatogenic failure 39	skos:exactMatch	DOID:0111926	spermatogenic failure 39	semapv:ManualMappingCuration	2024-02-18
MONDO:0032859	spermatogenic failure 40	skos:exactMatch	DOID:0111918	spermatogenic failure 40	semapv:ManualMappingCuration	2024-02-18
MONDO:0032863	spermatogenic failure 41	skos:exactMatch	DOID:0111912	spermatogenic failure 41	semapv:ManualMappingCuration	2024-02-18
MONDO:0032869	mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6	skos:exactMatch	DOID:0111749	mitochondrial complex V (ATP synthase) deficiency nuclear type 6	semapv:ManualMappingCuration	2023-11-19
MONDO:0032874	ciliary dyskinesia, primary, 43	skos:exactMatch	DOID:0111856	primary ciliary dyskinesia 43	semapv:ManualMappingCuration	2023-06-18
MONDO:0032891	aneurysm, intracranial berry, 12	skos:exactMatch	DOID:0080975	intracranial berry aneurysm 12	semapv:ManualMappingCuration	2023-06-18
MONDO:0032893	pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures	skos:exactMatch	DOID:0081266	pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures	semapv:ManualMappingCuration	2023-04-17
MONDO:0032895	developmental and epileptic encephalopathy, 83	skos:exactMatch	DOID:0112218	developmental and epileptic encephalopathy 83	semapv:ManualMappingCuration	2023-04-17
MONDO:0032896	spermatogenic failure 42	skos:exactMatch	DOID:0111923	spermatogenic failure 42	semapv:ManualMappingCuration	2023-03-17
MONDO:0032898	spermatogenic failure 43	skos:exactMatch	DOID:0111917	spermatogenic failure 43	semapv:ManualMappingCuration	2023-03-17
MONDO:0032899	neutropenia, severe congenital, 8, autosomal dominant	skos:exactMatch	DOID:0112135	severe congenital neutropenia 8	semapv:ManualMappingCuration	2023-06-18
MONDO:0032903	arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum	skos:exactMatch	DOID:0080980	arthrogryposis multiplex congenita-4	semapv:ManualMappingCuration	2023-06-18
MONDO:0032904	corneal dystrophy, Meesmann, 2	skos:exactMatch	DOID:0080671	Meesmann corneal dystrophy 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0032906	spastic paraplegia 82, autosomal recessive	skos:exactMatch	DOID:0112343	hereditary spastic paraplegia 82	semapv:ManualMappingCuration	2023-06-18
MONDO:0032910	mitochondrial complex 1 deficiency, nuclear type 34	skos:exactMatch	DOID:0112091	nuclear type mitochondrial complex I deficiency 34	semapv:ManualMappingCuration	2023-06-18
MONDO:0032911	hearing loss, autosomal dominant 75	skos:exactMatch	DOID:0112166	autosomal dominant nonsyndromic deafness 75	semapv:ManualMappingCuration	2023-06-18
MONDO:0032912	Coffin-Siris syndrome 11	skos:exactMatch	DOID:0112372	Coffin-Siris syndrome 11	semapv:ManualMappingCuration	2023-03-17
MONDO:0032914	ciliary dyskinesia, primary, 44	skos:exactMatch	DOID:0111851	primary ciliary dyskinesia 44	semapv:ManualMappingCuration	2023-06-18
MONDO:0032915	long QT syndrome 16	skos:exactMatch	DOID:0070533	long QT syndrome 16	semapv:ManualMappingCuration	2024-04-21
MONDO:0032917	hearing loss, autosomal dominant 76	skos:exactMatch	DOID:0112167	autosomal dominant nonsyndromic deafness 76	semapv:ManualMappingCuration	2023-06-18
MONDO:0032918	developmental and epileptic encephalopathy, 84	skos:exactMatch	DOID:0112219	developmental and epileptic encephalopathy 84	semapv:ManualMappingCuration	2023-04-17
MONDO:0032923	spinocerebellar ataxia, autosomal recessive 28	skos:exactMatch	DOID:0070409	autosomal recessive spinocerebellar ataxia 28	semapv:ManualMappingCuration	2023-07-09
MONDO:0032924	ciliary dyskinesia, primary, 45	skos:exactMatch	DOID:0111857	primary ciliary dyskinesia 45	semapv:ManualMappingCuration	2023-06-18
MONDO:0032926	sandestig-stefanova syndrome	skos:exactMatch	DOID:0081272	Sandestig-Stefanova syndrome	semapv:ManualMappingCuration	2023-04-17
MONDO:0032931	pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal	skos:exactMatch	DOID:0081396	neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0032932	mitochondrial DNA depletion syndrome 18	skos:exactMatch	DOID:0070449	mitochondrial DNA depletion syndrome 18	semapv:ManualMappingCuration	2024-04-21
MONDO:0032936	myopathy, congenital, with respiratory insufficiency and bone fractures	skos:exactMatch	DOID:0081343	congenital myopathy 9A	semapv:ManualMappingCuration	2023-07-09
MONDO:0032937	myopathy, congenital proximal, with minicore lesions	skos:exactMatch	DOID:0081344	congenital myopathy 9B	semapv:ManualMappingCuration	2023-07-09
MONDO:0032940	retinitis pigmentosa 88	skos:exactMatch	DOID:0112145	retinitis pigmentosa 88	semapv:ManualMappingCuration	2023-03-17
MONDO:0033006	Galloway-Mowat syndrome 2, X-linked	skos:exactMatch	DOID:0080244	Galloway-Mowat syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0033014	erythrokeratodermia variabilis et progressiva 4	skos:exactMatch	DOID:0080250	erythrokeratodermia variabilis et progressiva 4	semapv:ManualMappingCuration	2023-03-17
MONDO:0033043	spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy	skos:exactMatch	DOID:0080252	spastic ataxia 8	semapv:ManualMappingCuration	2023-03-17
MONDO:0033201	hearing loss, autosomal recessive 57	skos:exactMatch	DOID:0111635	autosomal recessive nonsyndromic deafness 57	semapv:ManualMappingCuration	2023-03-17
MONDO:0033204	ciliary dyskinesia, primary, 37	skos:exactMatch	DOID:0080266	primary ciliary dyskinesia 37	semapv:ManualMappingCuration	2023-03-17
MONDO:0033280	nephrotic syndrome 16	skos:exactMatch	DOID:0080272	nephrotic syndrome type 16	semapv:ManualMappingCuration	2024-04-21
MONDO:0033361	developmental and epileptic encephalopathy, 52	skos:exactMatch	DOID:0080455	developmental and epileptic encephalopathy 52	semapv:ManualMappingCuration	2023-03-17
MONDO:0033363	developmental and epileptic encephalopathy, 54	skos:exactMatch	DOID:0080418	developmental and epileptic encephalopathy 54	semapv:ManualMappingCuration	2023-04-17
MONDO:0033364	developmental and epileptic encephalopathy, 55	skos:exactMatch	DOID:0080283	developmental and epileptic encephalopathy 55	semapv:ManualMappingCuration	2023-11-19
MONDO:0033368	developmental and epileptic encephalopathy, 59	skos:exactMatch	DOID:0080291	developmental and epileptic encephalopathy 59	semapv:ManualMappingCuration	2023-11-19
MONDO:0033370	developmental and epileptic encephalopathy, 61	skos:exactMatch	DOID:0080434	developmental and epileptic encephalopathy 61	semapv:ManualMappingCuration	2023-11-19
MONDO:0033371	developmental and epileptic encephalopathy, 62	skos:exactMatch	DOID:0080420	developmental and epileptic encephalopathy 62	semapv:ManualMappingCuration	2023-11-19
MONDO:0033374	developmental and epileptic encephalopathy, 65	skos:exactMatch	DOID:0080430	developmental and epileptic encephalopathy 65	semapv:ManualMappingCuration	2023-03-17
MONDO:0033482	spinocerebellar ataxia 47	skos:exactMatch	DOID:0111743	cerebellar ataxia type 47	semapv:ManualMappingCuration	2023-03-17
MONDO:0033533	combined oxidative phosphorylation deficiency 45	skos:exactMatch	DOID:0112113	combined oxidative phosphorylation deficiency 45	semapv:ManualMappingCuration	2023-03-17
MONDO:0033534	combined oxidative phosphorylation deficiency 46	skos:exactMatch	DOID:0112115	combined oxidative phosphorylation deficiency 46	semapv:ManualMappingCuration	2023-03-17
MONDO:0033537	combined oxidative phosphorylation deficiency 47	skos:exactMatch	DOID:0112114	combined oxidative phosphorylation deficiency 47	semapv:ManualMappingCuration	2023-03-17
MONDO:0033541	immunodeficiency 69	skos:exactMatch	DOID:0112006	immunodeficiency 69	semapv:ManualMappingCuration	2023-03-17
MONDO:0033542	immunodeficiency 70	skos:exactMatch	DOID:0112005	immunodeficiency 70	semapv:ManualMappingCuration	2023-03-17
MONDO:0033545	mitochondrial DNA depletion syndrome 19	skos:exactMatch	DOID:0070450	mitochondrial DNA depletion syndrome 19	semapv:ManualMappingCuration	2024-04-21
MONDO:0033548	myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies	skos:exactMatch	DOID:0081349	congenital myopathy 17	semapv:ManualMappingCuration	2023-07-09
MONDO:0033549	optic atrophy 12	skos:exactMatch	DOID:0080840	optic atrophy 12	semapv:ManualMappingCuration	2023-03-17
MONDO:0033551	immunodeficiency 72 with autoinflammation	skos:exactMatch	DOID:0112015	immunodeficiency 72	semapv:ManualMappingCuration	2023-04-17
MONDO:0033554	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia	skos:exactMatch	DOID:0112061	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia	semapv:ManualMappingCuration	2023-03-17
MONDO:0033555	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia	skos:exactMatch	DOID:0112062	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia	semapv:ManualMappingCuration	2023-03-17
MONDO:0033556	muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15	skos:exactMatch	DOID:0112376	muscular dystrophy-dystroglycanopathy type B15	semapv:ManualMappingCuration	2023-06-18
MONDO:0033560	mitochondrial complex 1 deficiency, nuclear type 35	skos:exactMatch	DOID:0112139	nuclear type mitochondrial complex I deficiency 35	semapv:ManualMappingCuration	2023-06-18
MONDO:0033563	retinitis pigmentosa 90	skos:exactMatch	DOID:0112147	retinitis pigmentosa 90	semapv:ManualMappingCuration	2023-03-17
MONDO:0033566	combined oxidative phosphorylation deficiency 48	skos:exactMatch	DOID:0112112	combined oxidative phosphorylation deficiency 48	semapv:ManualMappingCuration	2023-03-17
MONDO:0033569	combined oxidative phosphorylation deficiency 49	skos:exactMatch	DOID:0112110	combined oxidative phosphorylation deficiency 49	semapv:ManualMappingCuration	2023-03-17
MONDO:0033570	combined oxidative phosphorylation deficiency 50	skos:exactMatch	DOID:0112111	combined oxidative phosphorylation deficiency 50	semapv:ManualMappingCuration	2023-03-17
MONDO:0033614	spastic paraplegia 83, autosomal recessive	skos:exactMatch	DOID:0112346	hereditary spastic paraplegia 83	semapv:ManualMappingCuration	2023-06-18
MONDO:0033615	coenzyme q10 deficiency, primary, 9	skos:exactMatch	DOID:0112138	primary coenzyme Q10 deficiency 9	semapv:ManualMappingCuration	2023-06-18
MONDO:0033618	Vissers-Bodmer syndrome	skos:exactMatch	DOID:0081397	Vissers-Bodmer syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0033620	myofibrillar myopathy 10	skos:exactMatch	DOID:0112108	myofibrillar myopathy 10	semapv:ManualMappingCuration	2023-03-17
MONDO:0033622	spermatogenic failure 44	skos:exactMatch	DOID:0112109	spermatogenic failure 44	semapv:ManualMappingCuration	2023-03-17
MONDO:0033630	neurodevelopmental disorder with speech impairment and dysmorphic facies	skos:exactMatch	DOID:0070417	neurodevelopmental disorder with speech impairment and dysmorphic facies	semapv:ManualMappingCuration	2023-07-09
MONDO:0033631	combined oxidative phosphorylation deficiency 51	skos:exactMatch	DOID:0112137	combined oxidative phosphorylation deficiency 51	semapv:ManualMappingCuration	2023-11-19
MONDO:0033635	mitochondrial complex 4 deficiency, nuclear type 3	skos:exactMatch	DOID:0070492	mitochondrial complex IV deficiency nuclear type 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0033636	mitochondrial complex 4 deficiency, nuclear type 4	skos:exactMatch	DOID:0070493	mitochondrial complex IV deficiency nuclear type 4	semapv:ManualMappingCuration	2024-04-21
MONDO:0033637	mitochondrial complex 4 deficiency, nuclear type 7	skos:exactMatch	DOID:0070494	mitochondrial complex IV deficiency nuclear type 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0033638	mitochondrial complex 4 deficiency, nuclear type 8	skos:exactMatch	DOID:0070495	mitochondrial complex IV deficiency nuclear type 8	semapv:ManualMappingCuration	2024-04-21
MONDO:0033639	mitochondrial complex 4 deficiency, nuclear type 10	skos:exactMatch	DOID:0070496	mitochondrial complex IV deficiency nuclear type 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0033643	inflammatory bowel disease 30	skos:exactMatch	DOID:0112154	inflammatory bowel disease 30	semapv:ManualMappingCuration	2023-04-17
MONDO:0033645	mitochondrial complex 4 deficiency, nuclear type 11	skos:exactMatch	DOID:0070497	mitochondrial complex IV deficiency nuclear type 11	semapv:ManualMappingCuration	2024-04-21
MONDO:0033646	mitochondrial complex 4 deficiency, nuclear type 12	skos:exactMatch	DOID:0070498	mitochondrial complex IV deficiency nuclear type 12	semapv:ManualMappingCuration	2024-04-21
MONDO:0033649	mitochondrial complex 4 deficiency, nuclear type 14	skos:exactMatch	DOID:0070499	mitochondrial complex IV deficiency nuclear type 14	semapv:ManualMappingCuration	2024-04-21
MONDO:0033650	mitochondrial complex 4 deficiency, nuclear type 15	skos:exactMatch	DOID:0070500	mitochondrial complex IV deficiency nuclear type 15	semapv:ManualMappingCuration	2024-04-21
MONDO:0033651	mitochondrial complex 4 deficiency, nuclear type 16	skos:exactMatch	DOID:0070501	mitochondrial complex IV deficiency nuclear type 16	semapv:ManualMappingCuration	2024-04-21
MONDO:0033652	mitochondrial complex 4 deficiency, nuclear type 17	skos:exactMatch	DOID:0070502	mitochondrial complex IV deficiency nuclear type 17	semapv:ManualMappingCuration	2024-04-21
MONDO:0033653	mitochondrial complex 4 deficiency, nuclear type 18	skos:exactMatch	DOID:0070503	mitochondrial complex IV deficiency nuclear type 18	semapv:ManualMappingCuration	2024-04-21
MONDO:0033654	mitochondrial complex 4 deficiency, nuclear type 19	skos:exactMatch	DOID:0070504	mitochondrial complex IV deficiency nuclear type 19	semapv:ManualMappingCuration	2024-04-21
MONDO:0033655	mitochondrial complex 4 deficiency, nuclear type 20	skos:exactMatch	DOID:0070505	mitochondrial complex IV deficiency nuclear type 20	semapv:ManualMappingCuration	2024-04-21
MONDO:0033656	mitochondrial complex 4 deficiency, nuclear type 21	skos:exactMatch	DOID:0070506	mitochondrial complex IV deficiency nuclear type 21	semapv:ManualMappingCuration	2024-04-21
MONDO:0033657	leukodystrophy, hypomyelinating, 20	skos:exactMatch	DOID:0112153	hypomyelinating leukodystrophy 20	semapv:ManualMappingCuration	2023-11-19
MONDO:0033665	hearing loss, autosomal dominant 78	skos:exactMatch	DOID:0112159	autosomal dominant nonsyndromic deafness 78	semapv:ManualMappingCuration	2023-06-18
MONDO:0033668	hearing loss, autosomal dominant 79	skos:exactMatch	DOID:0112160	autosomal dominant nonsyndromic deafness 79	semapv:ManualMappingCuration	2023-11-19
MONDO:0033670	hearing loss, autosomal recessive 116	skos:exactMatch	DOID:0112162	autosomal recessive nonsyndromic deafness 116	semapv:ManualMappingCuration	2023-11-19
MONDO:0033671	spermatogenic failure 45	skos:exactMatch	DOID:0112163	spermatogenic failure 45	semapv:ManualMappingCuration	2023-03-17
MONDO:0033673	spermatogenic failure 46	skos:exactMatch	DOID:0112164	spermatogenic failure 46	semapv:ManualMappingCuration	2023-03-17
MONDO:0033946	hereditary angioedema with C1Inh deficiency	skos:exactMatch	DOID:0080939	hereditary angioedema type I	semapv:ManualMappingCuration	2023-06-18
MONDO:0035944	B-lymphoblastic leukemia/lymphoma with hypodiploidy	skos:exactMatch	DOID:0080647	B-lymphoblastic leukemia/lymphoma with hypodiploidy	semapv:ManualMappingCuration	2023-11-19
MONDO:0036484	Charcot-Marie-Tooth disease, dominant intermediate G	skos:exactMatch	DOID:0080294	Charcot-Marie-Tooth disease dominant intermediate G	semapv:ManualMappingCuration	2023-03-17
MONDO:0040500	glycosylphosphatidylinositol biosynthesis defect 16	skos:exactMatch	DOID:0081223	glycosylphosphatidylinositol biosynthesis defect 16	semapv:ManualMappingCuration	2023-03-17
MONDO:0042487	uterine cervix carcinoma in situ	skos:exactMatch	DOID:8991	cervix uteri carcinoma in situ	semapv:ManualMappingCuration	2023-03-17
MONDO:0042490	neutropenia, severe congenital, 1, autosomal dominant	skos:exactMatch	DOID:0080625	severe congenital neutropenia 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0042981	aortic valve stenosis	skos:exactMatch	DOID:1712	aortic valve stenosis	semapv:ManualMappingCuration	2023-03-17
MONDO:0044212	chronic idiopathic urticaria	skos:exactMatch	DOID:0080749	chronic spontaneous urticaria	semapv:ManualMappingCuration	2024-04-21
MONDO:0044300	familial adenomatous polyposis 4	skos:exactMatch	DOID:0080412	familial adenomatous polyposis 4	semapv:ManualMappingCuration	2024-06-23
MONDO:0044302	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder	skos:exactMatch	DOID:0112247	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder	semapv:ManualMappingCuration	2023-03-17
MONDO:0044311	brachycephaly, trichomegaly, and developmental delay	skos:exactMatch	DOID:0070415	brachycephaly, trichomegaly, and developmental delay	semapv:ManualMappingCuration	2023-11-19
MONDO:0044313	intellectual disability, autosomal recessive 60	skos:exactMatch	DOID:0081222	autosomal recessive intellectual developmental disorder 60	semapv:ManualMappingCuration	2023-11-19
MONDO:0044315	craniosynostosis 7	skos:exactMatch	DOID:0060912	craniosynostosis 7	semapv:ManualMappingCuration	2024-04-21
MONDO:0044326	developmental delay and seizures with or without movement abnormalities	skos:exactMatch	DOID:0080473	developmental delay and seizures with or without movement abnormalities	semapv:ManualMappingCuration	2023-03-17
MONDO:0044634	retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome	skos:exactMatch	DOID:0081175	short stature, hearing loss, retinitis pigmentosa, and distinctive facies	semapv:ManualMappingCuration	2023-11-19
MONDO:0044646	early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome	skos:exactMatch	DOID:0070423	early onset progressive encephalopathy with brain atrophy and thin corpus callosum	semapv:ManualMappingCuration	2023-07-09
MONDO:0044701	childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder	skos:exactMatch	DOID:0070474	childhood-onset neurodegeneration with brain atrophy	semapv:ManualMappingCuration	2024-04-21
MONDO:0044721	severe combined immunodeficiency due to LAT deficiency	skos:exactMatch	DOID:0111983	immunodeficiency 52	semapv:ManualMappingCuration	2023-11-19
MONDO:0044723	3-methylglutaconic aciduria type 8	skos:exactMatch	DOID:0070000	3-methylglutaconic aciduria type 8	semapv:ManualMappingCuration	2023-11-19
MONDO:0044724	3-methylglutaconic aciduria type 9	skos:exactMatch	DOID:0070002	3-methylglutaconic aciduria type 9	semapv:ManualMappingCuration	2023-03-17
MONDO:0044725	combined immunodeficiency due to GINS1 deficiency	skos:exactMatch	DOID:0111993	immunodeficiency 55	semapv:ManualMappingCuration	2023-04-17
MONDO:0044767	childhood adrenal gland pheochromocytoma	skos:exactMatch	DOID:0070325	malignant childhood adrenal gland pheochromocytoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0044792	large congenital melanocytic nevus	skos:exactMatch	DOID:0111359	large congenital melanocytic nevus	semapv:ManualMappingCuration	2023-03-17
MONDO:0044923	acute myeloid leukemia with mutated NPM1	skos:exactMatch	DOID:0081089	acute myeloid leukemia with mutated NPM1	semapv:ManualMappingCuration	2023-11-19
MONDO:0045059	cribriform carcinoma of breast	skos:exactMatch	DOID:5675	cribriform carcinoma	semapv:ManualMappingCuration	2024-04-21
MONDO:0054559	congenital disorder of glycosylation, type IIq	skos:exactMatch	DOID:0070269	congenital disorder of glycosylation type IIq	semapv:ManualMappingCuration	2023-03-17
MONDO:0054615	spermatogenic failure 18	skos:exactMatch	DOID:0070165	spermatogenic failure 18	semapv:ManualMappingCuration	2024-02-18
MONDO:0054691	immunodeficiency, common variable, 14	skos:exactMatch	DOID:0081156	common variable immunodeficiency 14	semapv:ManualMappingCuration	2023-06-18
MONDO:0054695	myopathy, centronuclear, 6, with fiber-type disproportion	skos:exactMatch	DOID:0111221	centronuclear myopathy 6 with fiber-type disproportion	semapv:ManualMappingCuration	2023-03-17
MONDO:0054696	immunodeficiency 53	skos:exactMatch	DOID:0111992	immunodeficiency 53	semapv:ManualMappingCuration	2024-02-18
MONDO:0054699	proteasome-associated autoinflammatory syndrome 3	skos:exactMatch	DOID:0060916	proteosome-associated autoinflammatory syndrome 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0054700	proteasome-associated autoinflammatory syndrome 2	skos:exactMatch	DOID:0060914	proteosome-associated autoinflammatory syndrome 2	semapv:ManualMappingCuration	2024-04-21
MONDO:0054701	Kleefstra syndrome 2	skos:exactMatch	DOID:0080598	Kleefstra syndrome 2	semapv:ManualMappingCuration	2023-03-17
MONDO:0054723	spermatogenic failure 19	skos:exactMatch	DOID:0070170	spermatogenic failure 19	semapv:ManualMappingCuration	2024-02-18
MONDO:0054724	spermatogenic failure 20	skos:exactMatch	DOID:0070166	spermatogenic failure 20	semapv:ManualMappingCuration	2024-02-18
MONDO:0054726	spermatogenic failure 22	skos:exactMatch	DOID:0070177	spermatogenic failure 22	semapv:ManualMappingCuration	2023-03-17
MONDO:0054727	spermatogenic failure 23	skos:exactMatch	DOID:0070181	spermatogenic failure 23	semapv:ManualMappingCuration	2023-03-17
MONDO:0054728	spermatogenic failure 24	skos:exactMatch	DOID:0111929	spermatogenic failure 24	semapv:ManualMappingCuration	2023-03-17
MONDO:0054729	spermatogenic failure 25	skos:exactMatch	DOID:0111920	spermatogenic failure 25	semapv:ManualMappingCuration	2023-03-17
MONDO:0054730	spermatogenic failure 26	skos:exactMatch	DOID:0111924	spermatogenic failure 26	semapv:ManualMappingCuration	2023-03-17
MONDO:0054731	spermatogenic failure 27	skos:exactMatch	DOID:0111928	spermatogenic failure 27	semapv:ManualMappingCuration	2024-02-18
MONDO:0054732	spermatogenic failure 28	skos:exactMatch	DOID:0111916	spermatogenic failure 28	semapv:ManualMappingCuration	2023-03-17
MONDO:0054733	spermatogenic failure 29	skos:exactMatch	DOID:0111930	spermatogenic failure 29	semapv:ManualMappingCuration	2023-03-17
MONDO:0054740	blepharocheilodontic syndrome 1	skos:exactMatch	DOID:0080345	blepharocheilodontic syndrome 1	semapv:ManualMappingCuration	2024-06-23
MONDO:0054741	combined oxidative phosphorylation deficiency 34	skos:exactMatch	DOID:0111497	combined oxidative phosphorylation deficiency 34	semapv:ManualMappingCuration	2023-03-17
MONDO:0054742	combined oxidative phosphorylation deficiency 35	skos:exactMatch	DOID:0111464	combined oxidative phosphorylation deficiency 35	semapv:ManualMappingCuration	2023-03-17
MONDO:0054750	amyotrophic lateral sclerosis, susceptibility to, 24	skos:exactMatch	DOID:0081378	amyotrophic lateral sclerosis type 24	semapv:ManualMappingCuration	2024-04-21
MONDO:0054781	combined oxidative phosphorylation deficiency 36	skos:exactMatch	DOID:0111482	combined oxidative phosphorylation deficiency 36	semapv:ManualMappingCuration	2023-03-17
MONDO:0054782	leukodystrophy, hypomyelinating, 15	skos:exactMatch	DOID:0070398	hypomyelinating leukodystrophy 15	semapv:ManualMappingCuration	2023-07-09
MONDO:0054785	multiple mitochondrial dysfunctions syndrome 6	skos:exactMatch	DOID:0070332	multiple mitochondrial dysfunctions syndrome 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0054801	erythrocytosis, familial, 6	skos:exactMatch	DOID:0111632	familial erythrocytosis 6	semapv:ManualMappingCuration	2023-03-17
MONDO:0054813	Ehlers-Danlos syndrome, classic-like, 2	skos:exactMatch	DOID:0080732	Ehlers-Danlos syndrome classic-like 2	semapv:ManualMappingCuration	2023-06-18
MONDO:0054817	leukodystrophy, hypomyelinating, 17	skos:exactMatch	DOID:0070404	hypomyelinating leukodystrophy 17	semapv:ManualMappingCuration	2023-07-09
MONDO:0054833	charcot-marie-tooth disease, axonal, type 2DD	skos:exactMatch	DOID:0111558	Charcot-Marie-Tooth disease type 2DD	semapv:ManualMappingCuration	2023-03-17
MONDO:0054835	classic dopamine transporter deficiency syndrome	skos:exactMatch	DOID:0070489	classic dopamine transporter deficiency syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0054842	polycystic kidney disease 6 with or without polycystic liver disease	skos:exactMatch	DOID:0060951	polycystic kidney disease 6	semapv:ManualMappingCuration	2024-07-21
MONDO:0054843	ciliary dyskinesia, primary, 38	skos:exactMatch	DOID:0111852	primary ciliary dyskinesia 38	semapv:ManualMappingCuration	2023-06-18
MONDO:0054845	developmental and epileptic encephalopathy, 66	skos:exactMatch	DOID:0080446	developmental and epileptic encephalopathy 66	semapv:ManualMappingCuration	2023-03-17
MONDO:0054852	peeling skin syndrome 6	skos:exactMatch	DOID:0070525	peeling skin syndrome 6	semapv:ManualMappingCuration	2024-04-21
MONDO:0054860	hearing loss, autosomal recessive 110	skos:exactMatch	DOID:0111644	autosomal recessive nonsyndromic deafness 110	semapv:ManualMappingCuration	2023-03-17
MONDO:0056797	neurodevelopmental disorder with midbrain and hindbrain malformations	skos:exactMatch	DOID:0080312	neurodevelopmental disorder with midbrain and hindbrain malformations	semapv:ManualMappingCuration	2023-03-17
MONDO:0056804	benign neoplasm of peripheral nervous system	skos:exactMatch	DOID:0080320	peripheral nervous system benign neoplasm	semapv:ManualMappingCuration	2023-03-17
MONDO:0056806	non-small cell squamous lung carcinoma	skos:exactMatch	DOID:0080521	lung non-squamous non-small cell carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0060491	neurodevelopmental disorder with involuntary movements	skos:exactMatch	DOID:0112276	neurodevelopmental disorder with involuntary movements	semapv:ManualMappingCuration	2023-03-17
MONDO:0060533	microcephaly, short stature, and limb abnormalities	skos:exactMatch	DOID:0081431	microcephaly, short stature, and limb abnormalities	semapv:ManualMappingCuration	2024-05-19
MONDO:0060549	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay	skos:exactMatch	DOID:0112359	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay	semapv:ManualMappingCuration	2023-03-17
MONDO:0060583	platelet abnormalities with eosinophilia and immune-mediated inflammatory disease	skos:exactMatch	DOID:0112004	immunodeficiency 71	semapv:ManualMappingCuration	2023-04-17
MONDO:0060596	neurodevelopmental disorder with dysmorphic facies and distal limb anomalies	skos:exactMatch	DOID:0070514	neurodevelopmental disorder with dysmorphic facies and distal limb anomalies	semapv:ManualMappingCuration	2024-04-21
MONDO:0060631	Alkuraya-Kucinskas syndrome	skos:exactMatch	DOID:0111555	Alkuraya-Kucinskas syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0060640	neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy	skos:exactMatch	DOID:0060934	neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy	semapv:ManualMappingCuration	2024-04-21
MONDO:0060650	Leber congenital amaurosis with early-onset deafness	skos:exactMatch	DOID:0112240	Leber congenital amaurosis with early-onset deafness	semapv:ManualMappingCuration	2023-03-17
MONDO:0060664	neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities	skos:exactMatch	DOID:0081263	neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities	semapv:ManualMappingCuration	2023-04-17
MONDO:0060752	neurodevelopmental disorder with spasticity and poor growth	skos:exactMatch	DOID:0070421	neurodevelopmental disorder with spasticity and poor growth	semapv:ManualMappingCuration	2023-07-09
MONDO:0060759	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures	skos:exactMatch	DOID:0081327	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures	semapv:ManualMappingCuration	2023-04-17
MONDO:0100017	pityriasis rubra pilaris	skos:exactMatch	DOID:9212	pityriasis rubra pilaris	semapv:ManualMappingCuration	2023-03-17
MONDO:0100036	variable age onset epilepsy	skos:exactMatch	DOID:0050706	variable age at onset electroclinical syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0100058	hypervalinemia and hyperleucine-isoleucinemia	skos:exactMatch	DOID:0060950	hypervalinemia and hyperleucine-isoleucinemia	semapv:ManualMappingCuration	2024-07-21
MONDO:0100062	developmental and epileptic encephalopathy	skos:exactMatch	DOID:0050709	early infantile epileptic encephalopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0100062	developmental and epileptic encephalopathy	skos:exactMatch	DOID:0112202	developmental and epileptic encephalopathy	semapv:ManualMappingCuration	2023-03-17
MONDO:0100095	neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures	skos:exactMatch	DOID:0070352	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures	semapv:ManualMappingCuration	2023-03-17
MONDO:0100096	COVID-19	skos:exactMatch	DOID:0080600	COVID-19	semapv:ManualMappingCuration	2023-03-17
MONDO:0100101	fetal akinesia deformation sequence 1	skos:exactMatch	DOID:0111377	fetal akinesia deformation sequence syndrome 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0100116	Middle East respiratory syndrome	skos:exactMatch	DOID:0080642	Middle East respiratory syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0100130	adult acute respiratory distress syndrome	skos:exactMatch	DOID:11394	adult respiratory distress syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0100133	mitochondrial complex I deficiency	skos:exactMatch	DOID:0060536	mitochondrial complex I deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0100135	Dravet syndrome	skos:exactMatch	DOID:0080422	Dravet syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0100153	tubulinopathy	skos:exactMatch	DOID:0112227	tubulinopathy	semapv:ManualMappingCuration	2023-11-19
MONDO:0100164	permanent neonatal diabetes mellitus	skos:exactMatch	DOID:0060639	permanent neonatal diabetes mellitus	semapv:ManualMappingCuration	2023-03-17
MONDO:0100168	desmoid tumor caused by somatic mutation	skos:exactMatch	DOID:0111349	hereditary desmoid disease	semapv:ManualMappingCuration	2023-11-19
MONDO:0100186	GTP cyclohydrolase I deficiency with hyperphenylalaninemia	skos:exactMatch	DOID:0112225	BH4-deficient hyperphenylalaninemia B	semapv:ManualMappingCuration	2023-06-18
MONDO:0100211	growth hormone insensitivity with immune dysregulation 1, autosomal recessive	skos:exactMatch	DOID:0080836	growth hormone insensitivity syndrome with immune dysregulation 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0100213	IFAP syndrome 1, with or without BRESHECK syndrome	skos:exactMatch	DOID:0111821	ichthyosis follicularis-alopecia-photophobia syndrome 1	semapv:ManualMappingCuration	2023-04-17
MONDO:0100216	DICER1-related tumor predisposition	skos:exactMatch	DOID:0081063	DICER1 syndrome	semapv:ManualMappingCuration	2024-02-18
MONDO:0100218	arthrogryposis multiplex congenita 5	skos:exactMatch	DOID:0080981	arthrogryposis multiplex congenita-5	semapv:ManualMappingCuration	2023-06-18
MONDO:0100219	growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant	skos:exactMatch	DOID:0080837	growth hormone insensitivity syndrome with immune dysregulation 2	semapv:ManualMappingCuration	2023-04-17
MONDO:0100223	mitochondrial complex I deficiency, nuclear type	skos:exactMatch	DOID:0112065	nuclear type mitochondrial complex I deficiency	semapv:ManualMappingCuration	2023-06-18
MONDO:0100233	long COVID-19	skos:exactMatch	DOID:0080848	long COVID	semapv:ManualMappingCuration	2024-06-23
MONDO:0100244	paroxysmal nocturnal hemoglobinuria	skos:exactMatch	DOID:0060284	paroxysmal nocturnal hemoglobinuria	semapv:ManualMappingCuration	2023-03-17
MONDO:0100247	multiple congenital anomalies-hypotonia-seizures syndrome	skos:exactMatch	DOID:0080503	multiple congenital anomalies-hypotonia-seizures syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0100249	46,XX testicular disorder of sex development	skos:exactMatch	DOID:0111760	46,XX sex reversal	semapv:ManualMappingCuration	2023-03-17
MONDO:0100250	46,XX sex reversal 1	skos:exactMatch	DOID:0111761	46,XX sex reversal 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0100253	Roberts-SC phocomelia syndrome	skos:exactMatch	DOID:5325	Roberts syndrome	semapv:ManualMappingCuration	2024-02-18
MONDO:0100255	adenosine kinase deficiency	skos:exactMatch	DOID:0111038	hypermethioninemia due to adenosine kinase deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0100288	enhanced S-cone syndrome	skos:exactMatch	DOID:0090059	enhanced S-cone syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0100294	mitochondrial complex II deficiency, nuclear type 1	skos:exactMatch	DOID:0060537	mitochondrial complex II deficiency	semapv:ManualMappingCuration	2023-03-17
MONDO:0100296	Olmsted syndrome 1	skos:exactMatch	DOID:0112013	autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques	semapv:ManualMappingCuration	2023-04-17
MONDO:0100316	long QT syndrome 1	skos:exactMatch	DOID:0110644	long QT syndrome 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0100339	Friedreich ataxia	skos:exactMatch	DOID:12705	Friedreich ataxia	semapv:ManualMappingCuration	2023-03-17
MONDO:0100342	malignant glioma	skos:exactMatch	DOID:3070	high grade glioma	semapv:ManualMappingCuration	2023-03-17
MONDO:0100344	Bartter disease type 1	skos:exactMatch	DOID:0110142	Bartter disease type 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0100350	neuronopathy, distal hereditary motor, type 5	skos:exactMatch	DOID:0111203	autosomal dominant distal hereditary motor neuronopathy 5	semapv:ManualMappingCuration	2023-04-17
MONDO:0100352	episodic kinesigenic dyskinesia 1	skos:exactMatch	DOID:0090053	episodic kinesigenic dyskinesia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0100354	megacystis-microcolon-intestinal hypoperistalsis syndrome 1	skos:exactMatch	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome	semapv:ManualMappingCuration	2023-03-17
MONDO:0100382	acute myeloid leukemia, t(6;9)(p23;q34.1)	skos:exactMatch	DOID:0081080	acute myeloid leukemia with t(6;9) (p23;q34.1)	semapv:ManualMappingCuration	2023-06-18
MONDO:0100404	acute myeloid leukemia, MLL gene rearrangement	skos:exactMatch	DOID:0081094	acute myeloid leukemia with MLL rearrangement	semapv:ManualMappingCuration	2023-06-18
MONDO:0100409	acute myeloid leukemia, t(3;5)(q25;q34)	skos:exactMatch	DOID:0081092	acute myeloid leukemia with myelodysplasia-related changes	semapv:ManualMappingCuration	2023-06-18
MONDO:0100413	acute myeloid leukemia, biallelic CEBPA gene mutation	skos:exactMatch	DOID:0081090	acute myeloid leukemia with biallelic mutation of CEBPA	semapv:ManualMappingCuration	2023-06-18
MONDO:0100422	acute myeloid leukemia, RUNX1 gene mutation	skos:exactMatch	DOID:0081091	acute myeloid leukemia with mutated RUNX1	semapv:ManualMappingCuration	2023-06-18
MONDO:0100428	progressive bulbar palsy of childhood	skos:exactMatch	DOID:0080632	Fazio-Londe disease	semapv:ManualMappingCuration	2024-04-21
MONDO:0100431	migraine without aura	skos:exactMatch	DOID:12783	migraine without aura	semapv:ManualMappingCuration	2023-03-17
MONDO:0100510	spondyloepimetaphyseal dysplasia	skos:exactMatch	DOID:0080027	spondyloepimetaphyseal dysplasia	semapv:ManualMappingCuration	2023-03-17
MONDO:0100514	familial ovarian carcinoma	skos:exactMatch	DOID:6901	familiar ovarian carcinoma	semapv:ManualMappingCuration	2023-03-17
MONDO:0100522	hypotrichosis 4	skos:exactMatch	DOID:0110701	hypotrichosis 4	semapv:ManualMappingCuration	2023-11-19
MONDO:0600030	B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)	skos:exactMatch	DOID:0080649	B-lymphoblastic leukemia/lymphoma with TCF3-PBX1	semapv:ManualMappingCuration	2023-03-17
MONDO:0700089	paroxysmal nonkinesigenic dyskinesia 1	skos:exactMatch	DOID:0090049	paroxysmal nonkinesigenic dyskinesia 1	semapv:ManualMappingCuration	2023-03-17
MONDO:0700117	SLC6A3-related dopamine transporter deficiency syndrome	skos:exactMatch	DOID:0070487	dopamine transporter deficiency syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0700249	epidermolytic hyperkeratosis 1	skos:exactMatch	DOID:0081358	epidermolytic hyperkeratosis 1	semapv:ManualMappingCuration	2024-05-19
MONDO:0800025	Teebi hypertelorism syndrome 1	skos:exactMatch	DOID:0080698	Teebi hypertelorism syndrome 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0800026	central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease	skos:exactMatch	DOID:0060731	congenital central hypoventilation syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0800027	leukoencephalopathy, diffuse hereditary, with spheroids 1	skos:exactMatch	DOID:0080523	adult-onset leukoencephalopathy with axonal spheroids and pigmented glia	semapv:ManualMappingCuration	2023-11-19
MONDO:0800042	restrictive dermopathy 1	skos:exactMatch	DOID:0070369	restrictive dermopathy 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0800044	congenital disorder of deglycosylation 1	skos:exactMatch	DOID:0060728	NGLY1-deficiency	semapv:ManualMappingCuration	2023-11-19
MONDO:0800045	autoinflammatory syndrome, familial, Behcet-like 1	skos:exactMatch	DOID:0080944	familial Behcet-like autoinflammatory syndrome 1	semapv:ManualMappingCuration	2023-11-19
MONDO:0800368	cardiomyopathy, dilated, 1MM	skos:exactMatch	DOID:0081158	dilated cardiomyopathy 1MM	semapv:ManualMappingCuration	2023-11-19
MONDO:0800372	Joubert syndrome 29	skos:exactMatch	DOID:0080276	Joubert syndrome 29	semapv:ManualMappingCuration	2023-11-19
MONDO:0800438	developmental delay with short stature, dysmorphic facial features, and sparse hair 1	skos:exactMatch	DOID:0070477	diphthamide deficiency syndrome 1	semapv:ManualMappingCuration	2024-04-21
MONDO:0800445	Birt-Hogg-Dube syndrome 1	skos:exactMatch	DOID:0050676	Birt-Hogg-Dube syndrome	semapv:ManualMappingCuration	2024-06-23
MONDO:0800448	leukoencephalopathy with vanishing white matter	skos:exactMatch	DOID:0060868	leukoencephalopathy with vanishing white matter	semapv:ManualMappingCuration	2023-09-24
MONDO:0800452	congenital amegakaryocytic thrombocytopenia 1	skos:exactMatch	DOID:0090118	congenital amegakaryocytic thrombocytopenia	semapv:ManualMappingCuration	2024-06-23
MONDO:0800453	juvenile absence epilepsy	skos:exactMatch	DOID:0060172	juvenile absence epilepsy	semapv:ManualMappingCuration	2024-04-21
MONDO:0850093	absence epilepsy	skos:exactMatch	DOID:0070309	absence epilepsy	semapv:ManualMappingCuration	2023-04-17
MONDO:0850302	intracranial meningioma	skos:exactMatch	DOID:0060106	brain meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0850302	intracranial meningioma	skos:exactMatch	DOID:0080842	intracranial meningioma	semapv:ManualMappingCuration	2024-04-21
MONDO:0850349	astroblastoma, MN1-altered	skos:exactMatch	DOID:0080904	astroblastoma, MN1-altered	semapv:ManualMappingCuration	2024-02-18
MONDO:0850514	inclusion body myopathy and brain white matter abnormalities	skos:exactMatch	DOID:0081121	inclusion body myopathy and brain white matter abnormalities	semapv:ManualMappingCuration	2023-11-19
MONDO:0851095	KINSSHIP syndrome	skos:exactMatch	DOID:0112383	KINSSHIP syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0858921	EWSR1-negative small round cell tumor	skos:exactMatch	DOID:0081249	EWSR1-negative small round cell tumor	semapv:ManualMappingCuration	2024-08-18
MONDO:0858939	diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype	skos:exactMatch	DOID:0081277	diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype	semapv:ManualMappingCuration	2023-11-19
MONDO:0858940	infant-type hemispheric glioma	skos:exactMatch	DOID:0081278	infant-type hemispheric glioma	semapv:ManualMappingCuration	2023-08-20
MONDO:0858956	diffuse leptomeningeal glioneuronal tumor	skos:exactMatch	DOID:0081302	diffuse leptomeningeal glioneuronal tumor	semapv:ManualMappingCuration	2023-08-20
MONDO:0858958	high-grade astrocytoma with piloid features	skos:exactMatch	DOID:0081304	high-grade astrocytoma with piloid features	semapv:ManualMappingCuration	2024-02-18
MONDO:0859139	blepharophimosis-impaired intellectual development syndrome	skos:exactMatch	DOID:0081442	blepharophimosis-impaired intellectual development syndrome	semapv:ManualMappingCuration	2024-05-19
MONDO:0859152	neurodevelopmental disorder with cerebellar atrophy and motor dysfunction	skos:exactMatch	DOID:0070443	neurodevelopmental disorder with cerebellar atrophy and motor dysfunction	semapv:ManualMappingCuration	2024-08-18
MONDO:0859160	mitochondrial complex IV deficiency, nuclear type 22	skos:exactMatch	DOID:0070507	mitochondrial complex IV deficiency nuclear type 22	semapv:ManualMappingCuration	2024-04-21
MONDO:0859171	Luo-Schoch-Yamamoto syndrome	skos:exactMatch	DOID:0070416	Luo-Schoch-Yamamoto syndrome	semapv:ManualMappingCuration	2023-11-19
MONDO:0859179	neurodevelopmental disorder with dysmorphic facies and thin corpus callosum	skos:exactMatch	DOID:0070469	neurodevelopmental disorder with dysmorphic facies and thin corpus callosum	semapv:ManualMappingCuration	2024-08-18
MONDO:0859197	intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies	skos:exactMatch	DOID:0081262	intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies	semapv:ManualMappingCuration	2024-02-18
MONDO:0859208	Hengel-Maroofian-Schols syndrome	skos:exactMatch	DOID:0070408	Hengel-Maroofian-Schols syndrome	semapv:ManualMappingCuration	2024-02-18
MONDO:0859209	Zaki syndrome	skos:exactMatch	DOID:0070473	Zaki syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0859221	Yoon-Bellen neurodevelopmental syndrome	skos:exactMatch	DOID:0070468	Yoon-Bellen neurodevelopmental syndrome	semapv:ManualMappingCuration	2024-04-21
MONDO:0859226	craniotubular dysplasia, Ikegawa type	skos:exactMatch	DOID:0112340	craniotubular dysplasia Ikegawa type	semapv:ManualMappingCuration	2023-11-19
MONDO:0859228	combined oxidative phosphorylation deficiency 55	skos:exactMatch	DOID:0070428	combined oxidative phosphorylation deficiency 55	semapv:ManualMappingCuration	2024-04-21
MONDO:0859234	agammaglobulinemia 8b, autosomal recessive	skos:exactMatch	DOID:0081143	agammaglobulinemia 8B	semapv:ManualMappingCuration	2023-11-19
MONDO:0859235	auditory neuropathy, autosomal dominant 3	skos:exactMatch	DOID:0112373	autosomal dominant auditory neuropathy 3	semapv:ManualMappingCuration	2024-08-18
MONDO:0859280	developmental delay, hypotonia, and impaired language	skos:exactMatch	DOID:0070420	developmental delay, hypotonia, and impaired language	semapv:ManualMappingCuration	2024-06-23
MONDO:0859286	neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures	skos:exactMatch	DOID:0070536	neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures	semapv:ManualMappingCuration	2024-08-18
MONDO:0859295	neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties	skos:exactMatch	DOID:0070479	neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties	semapv:ManualMappingCuration	2024-04-21
MONDO:0859296	neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss	skos:exactMatch	DOID:0081324	neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss	semapv:ManualMappingCuration	2024-02-18
MONDO:0859300	neuronopathy, distal hereditary motor, autosomal dominant 10	skos:exactMatch	DOID:0081399	autosomal dominant distal hereditary motor neuronopathy 10	semapv:ManualMappingCuration	2024-04-21
MONDO:0859305	neurodevelopmental disorder with eye movement abnormalities and ataxia	skos:exactMatch	DOID:0081275	neurodevelopmental disorder with eye movement abnormalities and ataxia	semapv:ManualMappingCuration	2024-02-18
MONDO:0859355	inflammatory poikiloderma with hair abnormalities and acral keratoses	skos:exactMatch	DOID:0070510	inflammatory poikiloderma with hair abnormalities and acral keratoses	semapv:ManualMappingCuration	2024-04-21
MONDO:0859377	neurodevelopmental disorder with poor growth and behavioral abnormalities	skos:exactMatch	DOID:0081444	neurodevelopmental disorder with poor growth and behavioral abnormalities	semapv:ManualMappingCuration	2024-06-23
MONDO:0859514	congenital myopathy 18	skos:exactMatch	DOID:0081350	congenital myopathy 18	semapv:ManualMappingCuration	2024-02-18
MONDO:0859517	congenital myopathy 2b, severe infantile, autosomal recessive	skos:exactMatch	DOID:0081339	congenital myopathy 2B	semapv:ManualMappingCuration	2023-11-19
MONDO:0859518	leukodystrophy, hypomyelinating, 26, with chondrodysplasia	skos:exactMatch	DOID:0070403	hypomyelinating leukodystrophy 26	semapv:ManualMappingCuration	2023-11-19
MONDO:0859520	mitochondrial complex IV deficiency, nuclear type 23	skos:exactMatch	DOID:0070485	mitochondrial complex IV deficiency nuclear type 23	semapv:ManualMappingCuration	2024-04-21
MONDO:0859523	congenital myopathy 2c, severe infantile, autosomal dominant	skos:exactMatch	DOID:0081340	congenital myopathy 2C	semapv:ManualMappingCuration	2024-08-18
MONDO:0859578	lacrimoauriculodentodigital syndrome 3	skos:exactMatch	DOID:0081372	lacrimoauriculodentodigital syndrome 3	semapv:ManualMappingCuration	2024-04-21
MONDO:0859689	hepatobiliary benign neoplasm	skos:exactMatch	DOID:3117	hepatobiliary benign neoplasm	semapv:ManualMappingCuration	2024-03-24
MONDO:0956989	CIC-rearranged sarcoma	skos:exactMatch	DOID:0081250	CIC-rearranged sarcoma	semapv:ManualMappingCuration	2024-08-18
MONDO:0957196	diffuse midline glioma, H3 K27M-mutant	skos:exactMatch	DOID:0080684	diffuse midline glioma, H3 K27M-mutant	semapv:ManualMappingCuration	2024-08-18
MONDO:0957215	congenital myopathy 20	skos:exactMatch	DOID:0081352	congenital myopathy 20	semapv:ManualMappingCuration	2024-08-18
MONDO:0957221	spastic paraplegia 70, autosomal recessive	skos:exactMatch	DOID:0070454	hereditary spastic paraplegia 70	semapv:ManualMappingCuration	2024-06-23
MONDO:0957224	congenital myopathy 21 with early respiratory failure	skos:exactMatch	DOID:0081353	congenital myopathy 21	semapv:ManualMappingCuration	2024-04-21
MONDO:0957254	mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A	skos:exactMatch	DOID:0070461	mitochondrial complex V (ATP synthase) deficiency nuclear type 4A	semapv:ManualMappingCuration	2024-06-23
MONDO:0957265	congenital myopathy 22B, severe fetal	skos:exactMatch	DOID:0081355	congenital myopathy 22B	semapv:ManualMappingCuration	2024-04-21
MONDO:0957281	nemaline myopathy 5B, autosomal recessive, childhood-onset	skos:exactMatch	DOID:0081374	nemaline myopathy 5B	semapv:ManualMappingCuration	2024-04-21
MONDO:0957284	nemaline myopathy 5C, autosomal dominant	skos:exactMatch	DOID:0081375	nemaline myopathy 5C	semapv:ManualMappingCuration	2024-08-18
MONDO:0957308	spastic paraplegia 90A, autosomal dominant	skos:exactMatch	DOID:0070459	hereditary spastic paraplegia 90A	semapv:ManualMappingCuration	2024-04-21
MONDO:0957309	spastic paraplegia 90B, autosomal recessive	skos:exactMatch	DOID:0070460	hereditary spastic paraplegia 90B	semapv:ManualMappingCuration	2024-04-21
MONDO:0957317	hematuria, benign familial	skos:exactMatch	DOID:0111365	benign familial hematuria	semapv:ManualMappingCuration	2024-08-18
MONDO:0957385	dystonia 37, early-onset, with striatal lesions	skos:exactMatch	DOID:0060956	dystonia 37, early-onset with striatal lesions	semapv:ManualMappingCuration	2024-05-19
MONDO:0957386	neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities	skos:exactMatch	DOID:0081387	neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities	semapv:ManualMappingCuration	2024-04-21
MONDO:0957497	disabling pansclerotic morphea of childhood	skos:exactMatch	DOID:0081373	disabling pansclerotic morphea	semapv:ManualMappingCuration	2024-04-21
MONDO:0957541	neurodevelopmental disorder with hypotonia and speech delay, with or without seizures	skos:exactMatch	DOID:0070512	neurodevelopmental disorder with hypotonia and speech delay	semapv:ManualMappingCuration	2024-04-21
MONDO:0957576	parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development	skos:exactMatch	DOID:0070486	Parkinson's disease 25	semapv:ManualMappingCuration	2024-06-23
MONDO:0958184	epidermolytic hyperkeratosis 2	skos:exactMatch	DOID:0081359	epidermolytic hyperkeratosis 2	semapv:ManualMappingCuration	2024-05-19
MONDO:0958235	Ullrich congenital muscular dystrophy 1B	skos:exactMatch	DOID:0060942	Ullrich congenital muscular dystrophy 1B	semapv:ManualMappingCuration	2024-06-23
MONDO:0958236	Ullrich congenital muscular dystrophy 1C	skos:exactMatch	DOID:0060943	Ullrich congenital muscular dystrophy 1C	semapv:ManualMappingCuration	2024-06-23
MONDO:8000011	visceral neuropathy, familial, 1, autosomal recessive	skos:exactMatch	DOID:0080679	neuronal intestinal dysplasia type A	semapv:ManualMappingCuration	2023-11-19
Orphanet:101088	X-linked hyper-IgM syndrome	skos:exactMatch	DOID:6620	X-linked hyper IgM syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:107	BOR syndrome	skos:exactMatch	DOID:14702	branchiootorenal syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:122	Birt-Hogg-Dubé syndrome	skos:exactMatch	DOID:0050676	Birt-Hogg-Dube syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:140944	CLOVE syndrome	skos:exactMatch	DOID:0080351	CLOVES syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:145	Hereditary breast and ovarian cancer syndrome	skos:exactMatch	DOID:5683	hereditary breast ovarian cancer syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:167	Chédiak-Higashi syndrome	skos:exactMatch	DOID:2935	Chediak-Higashi syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:2053	Freeman-Sheldon syndrome	skos:exactMatch	DOID:0111604	Freeman-Sheldon syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:2053	Freeman-Sheldon syndrome	skos:exactMatch	DOID:0111605	distal arthrogryposis type 2A	semapv:ManualMappingCuration	2023-04-17
Orphanet:2189	Hydrolethalus	skos:exactMatch	DOID:0050779	hydrolethalus syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:2337	Non-epidermolytic palmoplantar keratoderma	skos:exactMatch	DOID:0050428	nonepidermolytic palmoplantar keratoderma	semapv:ManualMappingCuration	2023-03-17
Orphanet:26106	Familial gastric cancer	skos:exactMatch	DOID:0080763	diffuse gastric cancer	semapv:ManualMappingCuration	2023-03-17
Orphanet:2612	Linear nevus sebaceus syndrome	skos:exactMatch	DOID:0111530	linear nevus sebaceous syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:271861	Familial transthyretin-related amyloidosis	skos:exactMatch	DOID:0050638	transthyretin amyloidosis	semapv:ManualMappingCuration	2023-03-17
Orphanet:296	Enchondromatosis	skos:exactMatch	DOID:4624	Ollier disease	semapv:ManualMappingCuration	2023-03-17
Orphanet:321	Multiple osteochondromas	skos:exactMatch	DOID:206	hereditary multiple exostoses	semapv:ManualMappingCuration	2023-03-17
Orphanet:364	Glycogen storage disease due to glucose-6-phosphatase deficiency	skos:exactMatch	DOID:2749	glycogen storage disease Ia	semapv:ManualMappingCuration	2023-03-17
Orphanet:371433	Genetic periodic paralysis	skos:exactMatch	DOID:1029	familial periodic paralysis	semapv:ManualMappingCuration	2023-03-17
Orphanet:411602	Hereditary late-onset Parkinson disease	skos:exactMatch	DOID:0060892	late onset Parkinson's disease	semapv:ManualMappingCuration	2023-03-17
Orphanet:413	Hyperlipoproteinemia type 4	skos:exactMatch	DOID:1172	hyperlipoproteinemia type IV	semapv:ManualMappingCuration	2023-03-17
Orphanet:551	MERRF	skos:exactMatch	DOID:310	MERRF Syndrome	semapv:ManualMappingCuration	2023-03-17
Orphanet:678	Papillon-Lefèvre syndrome	skos:exactMatch	DOID:3389	Papillon-Lefevre disease	semapv:ManualMappingCuration	2023-03-17
Orphanet:70470	Hyperlipoproteinemia type 5	skos:exactMatch	DOID:1171	hyperlipoproteinemia type V	semapv:ManualMappingCuration	2023-03-17
Orphanet:733	Familial adenomatous polyposis	skos:exactMatch	DOID:0050424	familial adenomatous polyposis	semapv:ManualMappingCuration	2023-03-17
Orphanet:83419	Proximal spinal muscular atrophy type 3	skos:exactMatch	DOID:12376	juvenile spinal muscular atrophy	semapv:ManualMappingCuration	2023-03-17
Orphanet:846	Alpha-thalassemia	skos:exactMatch	DOID:1099	alpha thalassemia	semapv:ManualMappingCuration	2023-03-17
Orphanet:848	Beta-thalassemia	skos:exactMatch	DOID:12241	beta thalassemia	semapv:ManualMappingCuration	2023-03-17
Orphanet:85448	Familial amyloidosis, Finnish type	skos:exactMatch	DOID:0050637	Finnish type amyloidosis	semapv:ManualMappingCuration	2023-03-17
Orphanet:87884	Non-syndromic genetic deafness	skos:exactMatch	DOID:0050563	nonsyndromic deafness	semapv:ManualMappingCuration	2023-03-17
Orphanet:931	Acheiropodia	skos:exactMatch	DOID:0050603	acheiropody	semapv:ManualMappingCuration	2023-03-17
Orphanet:98757	Spinocerebellar ataxia type 3	skos:exactMatch	DOID:1440	Machado-Joseph disease	semapv:ManualMappingCuration	2023-03-17
PATO:0001340	hermaphrodite	skos:exactMatch	DOID:3763	hermaphroditism	semapv:ManualMappingCuration	2023-03-17