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DOID:699 - mitochondrial myopathy
Disease Ontology Definition:A myopathy that is characterized by mitochondrial dysfunction.
Synonyms: mitochondrial cytopathy, mitochondrial cytopathy (disorder),
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009637 - inborn mitochondrial myopathy |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
myopathy (is_a)