Juvenile polyposis syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:C537702
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3 genes/proteins associated with the disease Juvenile polyposis syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SMAD4 SMAD family member 4 2.88009
PTEN phosphatase and tensin homolog 2.88009
BMPR1A bone morphogenetic protein receptor, type IA 2.88009