/cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4
Rare Disease
MONDO:0014668
Also Known As
COA6 fatal infantile encephalocardiomyopathycardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 4cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4fatal infantile encephalocardiomyopathy caused by mutation in COA6mitochondrial complex IV deficiency, nuclear type 13CEMCOX4
Definition
Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA6 gene.
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