Disease association ontology term - MONDO:0012112 - hypertrophic cardiomyopathy 10
Term summary
- ID
- MONDO:0012112
- Name
- hypertrophic cardiomyopathy 10
- Ontology or CV name
- Disease association
- Definition
- Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene.
