COX deficiency, benign infantile mitochondrial myopathy

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Summary

Literature (0)

DOID:0081377 - COX deficiency, benign infantile mitochondrial myopathy

Disease Ontology Definition:A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles.

Synonyms: Isolated cytochrome C oxidase deficiency

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: fastkd2, cox10, coa8, taco1, coa3, coa5, pet100, cox6b1, cox20, sco1, coa7, cox8a, cox14

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): cytochrome-c oxidase deficiency disease (is_a)