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GTR Home > Conditions/Phenotypes > Coronary artery disease, autosomal dominant 2

Coronary artery disease, autosomal dominant 2

Summary

Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene. [from MONDO]

Available tests

12 tests are in the database for this condition.

Clinical tests (12 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ADCAD2, STHAG7, LRP6
    Summary: LDL receptor related protein 6

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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