|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An autosomal dominant disease that is characterized by predisposition to hamartomatous benign polyps in the gastrointestinal tract, specifically in the stomach, small intestine, colon, and rectum. (Human Disease Ontology, DOID_0050787)|
|Downloads & Tools|
3 genes/proteins associated with the disease Juvenile polyposis syndrome from the curated CTD Gene-Disease Associations dataset.