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

Last uploaded: September 7, 2023

Preferred Name	Congenital myopathy
ID	http://purl.bioontology.org/ontology/OMIM/MTHU065401
cui	C0270960
Manifestation of	http://purl.bioontology.org/ontology/OMIM/615438 http://purl.bioontology.org/ontology/OMIM/620161 http://purl.bioontology.org/ontology/OMIM/255300
notation	MTHU065401
prefLabel	Congenital myopathy
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU026723

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_97245	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://purl.obolibrary.org/obo/DOID_0081337	Human Disease Ontology / 人类疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0019952	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0019952	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.bioontology.org/ontology/ICD10/G71.2	International Classification of Diseases, Version 10 / 《国际疾病分类》第10版	CUI
http://purl.bmicc.cn/ontology/ICD10CN/G71.2	《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/G71.2	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI