familial adenomatous polyposis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease that is caused by mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer. (Human Disease Ontology, DOID_0050424)
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4 genes associated with the disease familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
APC adenomatous polyposis coli
MUTYH mutY homolog
PLA2G2A phospholipase A2, group IIA (platelets, synovial fluid)