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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),
Echinobase Genes : mt-nd1, mt-co1, mt-co2, mt-co3, mt-nd5, ND6, mt-cyb
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
myopathy (is_a)