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Summary Literature (0)
DOID:699 - mitochondrial myopathy

Disease Ontology Definition:A myopathy that is characterized by mitochondrial dysfunction.

Synonyms: mitochondrial cytopathy, mitochondrial cytopathy (disorder)

Xenbase Genes : polg, yars2, pus1, rrm2b, twnk, slc25a4, top3a, dguok, polg2, rnaseh1, dna2, mt-co1, chchd10, mt-cyb, mt-nd1, [+]

Mondo Disease Ontology (on Monarch Initiative):
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)