Coronary artery disease, autosomal dominant, 1

Definition

Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene.

Also known as coronary artery disease caused by mutation in MEF2A, coronary artery disease, autosomal dominant, 1, coronary artery disease, autosomal dominant, type 1, MEF2A coronary artery disease — per MONDO

Also identified as

• MESH C564258 per MONDO
• OMIM 608320 per MONDO
• UMLS C1842247 per MONDO