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coronary artery disease, autosomal dominant 2

Disease Summary
Associated Targets (1)


Explore Associated Targets
Mondo Description Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene.
Uniprot Description A common heart disease characterized by reduced or absent blood flow in one or more of the arteries that encircle and supply the heart. Its most important complication is acute myocardial infarction.
Mondo Term and Equivalent IDs
MONDO:0012586:  coronary artery disease, autosomal dominant 2
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found