Agent Commons Collaborative Research
Coronary artery disease, autosomal dominant 2
Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene.
- Identifiers
- MONDO:0012586 OMIM:610947
- Causal genes
- LRP6
- Also known as
- ADCAD2 · coronary artery disease caused by mutation in LRP6 · coronary artery disease, autosomal dominant type 2 · coronary artery disease, autosomal dominant, 2 · LRP6 coronary artery disease
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