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ENMitochondrial Complex Iv Deficiency, Nuclear Type 6 (MC4DN6)
Alias:
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2
Mc4dn6
Cemcox2
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency, Type 2
Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 2
Mitochondrial Complex Iv Deficiency Nuclear Type 6
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Mitochondrial Complex Iv Deficiency, Nuclear Type 6, is also known as cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2. An important gene associated with Mitochondrial Complex Iv Deficiency, Nuclear Type 6 is COX15 (Cytochrome C Oxidase Assembly Homolog COX15). Affiliated tissues include brain, and related phenotypes are hypotonia and retinopathy
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