COX deficiency, benign infantile mitochondrial myopathy Disease Ontology Browser

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COX deficiency, benign infantile mitochondrial myopathy (DOID:0081377)
Alliance: disease page
Synonyms: Isolated cytochrome C oxidase deficiency
Alt IDs: ORDO:254905, UMLS_CUI:C5779825
Definition: A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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