Disease association ontology term - MONDO:0012011 - coronary artery disease, autosomal dominant, 1
Term summary
- ID
- MONDO:0012011
- Name
- coronary artery disease, autosomal dominant, 1
- Ontology or CV name
- Disease association
- Definition
- Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene.
