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ENCox Deficiency, Infantile Mitochondrial Myopathy
Alias:
Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency
Fatal Infantile Cytochrome C Oxidase Deficiency
Fatal Infantile Cox Deficiency
Fatal Infantile Encephalocardiomyopathy
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Cox Deficiency, Infantile Mitochondrial Myopathy, also known as fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency, is related to mitochondrial complex iv deficiency, nuclear type 2 and mitochondrial complex iv deficiency, nuclear type 1. An important gene associated with Cox Deficiency, Infantile Mitochondrial Myopathy is SCO2 (Synthesis Of Cytochrome C Oxidase 2), and among its related pathways/superpathways are Metabolism and Nuclear events mediated by NFE2L2. Affiliated tissues include heart.
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