Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene.
Comprehensive, easy-to-understand information about this condition
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Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.
AI-curated news mentioning coronary artery disease, autosomal dominant 2
Updated Jan 6, 2026
Researchers have developed the first minimally invasive coronary artery bypass method, potentially providing a safer alternative for high-risk patients compared to traditional open-heart surgery. This breakthrough could significantly impact surgical approaches in cardiovascular care.