Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4

MONDO:0014668

Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA6 gene.

Also known as: COA6 fatal infantile encephalocardiomyopathy, cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 4, cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4, fatal infantile encephalocardiomyopathy caused by mutation in COA6, mitochondrial complex IV deficiency, nuclear type 13, CEMCOX4

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