Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023
Preferred Name

Mitochondrial myopathy

Definitions

A type of myopathy associated with mitochondrial disease and characterized by findings on biopsy such as ragged red muscle fibers. This is a bundled term that should not be used for future annotations.

ID

http://purl.obolibrary.org/obo/HP_0003737

comment

This is a bundled term that should not be used for future annotations.

database_cross_reference

SNOMEDCT_US:16851005

MSH:D017240

UMLS:C0162670

definition

A type of myopathy associated with mitochondrial disease and characterized by findings on biopsy such as ragged red muscle fibers.

has_alternative_id

HP:0008960

has_obo_namespace

human_phenotype

id

HP:0003737

label

Mitochondrial myopathy

notation

HP:0003737

prefLabel

Mitochondrial myopathy

treeView

http://purl.obolibrary.org/obo/HP_0003800

subClassOf

http://purl.obolibrary.org/obo/HP_0003800

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http://purl.obolibrary.org/obo/DOID_699 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_699 Human Disease Ontology / 人类疾病本体 LOOM
http://www.orpha.net/ORDO/Orphanet_206966 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://www.orpha.net/ORDO/Orphanet_206966 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU005171 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C101328 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM