Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库

Last uploaded: September 7, 2023

Preferred Name	Progressive muscular dystrophy
ID	http://purl.bioontology.org/ontology/OMIM/MTHU074661
cui	C0026850
Manifestation of	http://purl.bioontology.org/ontology/OMIM/226670
notation	MTHU074661
prefLabel	Progressive muscular dystrophy
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU026723

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0016106	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0016106	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.bioontology.org/ontology/ICD10/G71.0	International Classification of Diseases, Version 10 / 《国际疾病分类》第10版	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026850	MedlinePlus Health Topics / MedlinePlus网站健康主题	CUI
http://purl.bioontology.org/ontology/MESH/D009136	Medical Subject Headings / 医学主题词表	CUI
http://purl.bmicc.cn/ontology/ICD10CN/G71.0	《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/ICD10CM/G71.0	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI
http://www.orpha.net/ORDO/Orphanet_206644	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM