Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1

MONDO:0011451

Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the SCO2 gene.

Also known as: SCO2 fatal infantile encephalocardiomyopathy, cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 1, cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, fatal infantile encephalocardiomyopathy caused by mutation in SCO2, mitochondrial complex IV deficiency, nuclear type 2, CEMCOX1, cytochrome C oxidase deficiency, fatal infantile, with cardioencephalomyopathy

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