Juvenile polyposis syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/174900
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2 genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
BMPR1A bone morphogenetic protein receptor, type IA
SMAD4 SMAD family member 4