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Preferred Name

Mitochondrial Myopathy
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C101328
code

C101328
Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99147
Contributing_Source

NICHD

Cellosaurus
DEFINITION

Myopathy caused by mitochondrial abnormalities.
FULL_SYN

Mitochondrial Myopathy
label

Mitochondrial Myopathy
Preferred_Name

Mitochondrial Myopathy
prefixIRI

Thesaurus:C101328
prefLabel

Mitochondrial Myopathy
Semantic_Type

Disease or Syndrome
UMLS_CUI

C0162670
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84648
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Delete Mapping To Ontology Source
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://purl.obolibrary.org/obo/HP_0003737 Human Phenotype Ontology / 人类表型本体 LOOM