Disease association ontology term - MONDO:0014051 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
Term summary
- ID
- MONDO:0014051
- Name
- cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
- Ontology or CV name
- Disease association
- Definition
- Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COX15 gene.
