Coronary artery disease, autosomal dominant 2

Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene.

Also known as: LRP6 coronary artery disease, coronary artery disease caused by mutation in LRP6, coronary artery disease, autosomal dominant 2, coronary artery disease, autosomal dominant type 2, coronary artery disease, autosomal dominant, 2, ADCAD2

83 clinical trials for this condition and its sub-types, 0 tagged with Coronary artery disease, autosomal dominant 2 itself.