Disease association ontology term - MONDO:0014667 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
Term summary
- ID
- MONDO:0014667
- Name
- cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
- Ontology or CV name
- Disease association
- Definition
- Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA5 gene.
