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Cox Deficiency, Benign Infantile Mitochondrial Myopathy

Disease ID: disease_node_16766

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DbxrefGARD:48, ORDO:254905, UMLS_CUI:C5779825
SubclassofDOID_3762
Data SourceDOID
SynonymsIsolated cytochrome C oxidase deficiency
Doid LabelCOX deficiency, benign infantile mitochondrial myopathy
Doid DescriptionA cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles.
Disease Node Iddisease_node_16766
Doid IdDOID_0081377
LabelCox Deficiency, Benign Infantile Mitochondrial Myopathy