Human Phenotype Ontology 
Grandparent Node:
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Abnormality of digestive system morphology (HP:0025033)help
Grandparent Node:
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Abnormality of the gastrointestinal tract (HP:0011024)help
Parent Node:
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Morphological abnormality of the gastrointestinal tract (HP:0012718)help
..Starting node
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Gastrointestinal duplication (HP:0011140)help
Term ID: 11140
Name: Gastrointestinal duplication
Synonym: GI duplication
Definition: A spherical hollow structure with a smooth muscle coat, lined by a mucous membrane, and attached to any part of the gastrointestinal tract, from the base of the tongue to the anus.
Comments:
Reference: HP:0011140
Genes and Diseases:
 
       Child Nodes:
........expandGastric duplication (HP:0011139) help
........expandIntestinal duplication (HP:0100668) help
................... HP:0005223 Duplicated colon
........expandEsophageal duplication (HP:0100681) help

 Sister Nodes: 
..expandAbnormal esophagus morphology (HP:0002031) help
..expandAbnormal gastrointestinal vascular morphology (HP:0004296) help
..expandAbnormal intestine morphology (HP:0002242) help
..expandAbnormal stomach morphology (HP:0002577) help
..expandAnorectal anomaly (HP:0012732) help
..expandGastrointestinal atresia (HP:0002589) 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:0011140HP:0011140Gastrointestinal duplication0 CL E G H
HP:0011140HP:0100681Esophageal duplication1 CL E G H
HP:0011140HP:0100668Intestinal duplication1 CL E G H
HP:0011140HP:0011139Gastric duplication1 CL E G H
HP:0011140HP:0005223Duplicated colon2 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.