Human Phenotype Ontology 
Grandparent Node:
expandNeoplasm of the gastrointestinal tract (HP:0007378)help
Parent Node:
expandIntestinal polyp (HP:0005266)help
Parent Node:
expandNeoplasm of the small intestine (HP:0100833)help
..Starting node
..expandSmall intestinal polyp (HP:0012737)help
Term ID: 12737
Name: Small intestinal polyp
Synonym:
Definition: A discrete abnormal tissue mass that protrudes into the lumen of the small intestine and is attached to the intestinal wall either by a stalk, pedunculus, or a broad base.
Comments:
Reference: HP:0012737
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAdenocarcinoma of the small intestine (HP:0040274) help
..expandSmall intestine carcinoid (HP:0006722) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012737HP:0012737Small intestinal polyp0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.