Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3

Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA5 gene.

Also known as: COA5 fatal infantile encephalocardiomyopathy, cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 3, cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3, fatal infantile encephalocardiomyopathy caused by mutation in COA5, mitochondrial complex IV, deficiency, nuclear type 9, CEMCOX3

25 clinical trials for this condition and its sub-types, 0 tagged with Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 itself.