FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term juvenile polyposis syndrome ID (Ontology) DOID:0050787 (Human Disease)
Definition A gastrointestinal system disease that is characterized by predisposition to hamartomatous benign polyps in the gastrointestinal tract, specifically in the stomach, small intestine, colon, and rectum.
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Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      16
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 juvenile polyposis syndrome      19     11      1
 ameliorates | juvenile polyposis syndrome       4       --       --
 exacerbates | juvenile polyposis syndrome       1       --       --
 for disease ribbon | juvenile polyposis syndrome       --       2       --
 model of | juvenile polyposis syndrome      14      2       --
 DOES NOT model | juvenile polyposis syndrome       1       --       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_______
disease of anatomical entity         |
 |__gastrointestinal system disease__|
                                     juvenile polyposis syndrome  31 rec.
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Is a autosomal dominant disease
gastrointestinal system disease
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GARD:3065
MESH:C537702
MIM:174900