/cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
Rare Disease
MONDO:0014051
Also Known As
COX15 fatal infantile encephalocardiomyopathycardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 2cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2fatal infantile encephalocardiomyopathy caused by mutation in COX15mitochondrial complex IV deficiency, nuclear type 6CEMCOX2
Definition
Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COX15 gene.
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