/cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
Rare Disease
MONDO:0014667
Also Known As
COA5 fatal infantile encephalocardiomyopathycardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 3cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3fatal infantile encephalocardiomyopathy caused by mutation in COA5mitochondrial complex IV, deficiency, nuclear type 9CEMCOX3
Definition
Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA5 gene.
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