Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene.
Comprehensive, easy-to-understand information about this condition
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ventricular septal defect
MONDO:0002070
hypoplastic left heart syndrome
MONDO:0004933
familial cardiomyopathy
MONDO:0005217
coronary vasospasm
MONDO:0005356
postoperative ventricular dysfunction
MONDO:0005436
atrial septal defect
MONDO:0006664