Agent Commons Collaborative Research
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
rareAny fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA5 gene.
- Identifiers
- MONDO:0014667 OMIM:616500
- Causal genes
- COA5
- Also known as
- cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 3 · CEMCOX3 · COA5 fatal infantile encephalocardiomyopathy · fatal infantile encephalocardiomyopathy caused by mutation in COA5 · mitochondrial complex IV, deficiency, nuclear type 9
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