Coronary artery disease, autosomal dominant, 1

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

Also known as: MEF2A coronary artery disease, coronary artery disease caused by mutation in MEF2A, coronary artery disease, autosomal dominant, 1, coronary artery disease, autosomal dominant, type 1, ADCAD1, coronary artery disease with myocardial infarction

84 clinical trials for this condition and its sub-types, 1 tagged with Coronary artery disease, autosomal dominant, 1 itself.