Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2

Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COX15 gene.

Also known as: COX15 fatal infantile encephalocardiomyopathy, cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 2, cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, fatal infantile encephalocardiomyopathy caused by mutation in COX15, mitochondrial complex IV deficiency, nuclear type 6, CEMCOX2

25 clinical trials for this condition and its sub-types, 0 tagged with Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 itself.