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

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

25 clinical trials for this condition and its sub-types, 0 tagged with Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 itself.