You are using an outdated browser. Please upgrade your browser to improve your experience.

juvenile polyposis syndrome

Disease Summary
Associated Targets (5)
Tbio

3

Tchem

2


GARD Rare
Mondo Description Juvenile gastrointestinal polyposis (JIP) is a rare condition characterized by the presence of juvenile hamartomatous polyps in the gastrointestinal (GI) tract.
Uniprot Description Autosomal dominant gastrointestinal hamartomatous polyposis syndrome in which patients are at risk for developing gastrointestinal cancers. The lesions are typified by a smooth histological appearance, predominant stroma, cystic spaces and lack of a smooth muscle core. Multiple juvenile polyps usually occur in a number of Mendelian disorders. Sometimes, these polyps occur without associated features as in JPS; here, polyps tend to occur in the large bowel and are associated with an increased risk of colon and other gastrointestinal cancers.
Mondo Term and Equivalent IDs
MONDO:0017380:  juvenile polyposis syndrome
GARD:0003065: 
NCIT:C7754: 
Orphanet:2929: 
SCTID:9273005: 
UMLS:CN239474: