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

MONDO:0014051

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

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