Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023

Preferred Name	Potassium aggravated myotonia
Synonyms	Myotonia permanens
ID	http://purl.bioontology.org/ontology/MESH/C538353
altLabel	Myotonia permanens Sodium Channel Myotonia Myotonia congenita, atypical Myotonia, Potassium-Aggravated Potassium-Aggravated Myotonia Myotonia congenita, acetazolamide-responsive
cui	C2931826
HM	D009224
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D009224
MDA	20100825
MeSH Frequency	15
MMR	20131024
notation	C538353
prefLabel	Potassium aggravated myotonia
SC	3
TERMUI	T745532 T745534 T745533 T842305 T842306 T745535 T811343
TH	ORD (2010) OMIM (2013) GHR (2014)
tui	T047

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0018959	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0018959	Experimental Factor Ontology / 实验性因素本体	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122788	National Cancer Institute Thesaurus / 美国国家癌症研究所词典	LOOM
http://purl.bioontology.org/ontology/ICD10CM/G71.12	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI
http://purl.bioontology.org/ontology/ICD10CM/G71.19	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI
http://purl.bioontology.org/ontology/OMIM/608390	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://www.orpha.net/ORDO/Orphanet_612	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://purl.bioontology.org/ontology/OMIM/603967	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI