Coronary artery disease, autosomal dominant 2

Definition

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

Also known as 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, LRP6 coronary artery disease — per MONDO

Also identified as

• MESH C567045 per MONDO
• OMIM 610947 per MONDO
• UMLS C1970440 per MONDO