|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Gardner syndrome (GS) is a severe form of familial adenomatous polyposis (FAP, see this term) characterized by multiple adenomas in the colon and rectum associated with prominent extracolonic features including osteomas and multiple skin and soft tissue tumors (desmoid tumor; see this term). (Orphanet Rare Disease Ontology, Orphanet_79665)|
|Downloads & Tools|
1 genes associated with the Gardner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|APC||adenomatous polyposis coli|