Human Phenotype Ontology 
Grandparent Node:
expand
Morphological abnormality of the gastrointestinal tract (HP:0012718)help
Parent Node:
expand
Abnormal esophagus morphology (HP:0002031)help
..Starting node
..expand
Esophageal diverticulum (HP:0100628)help
Term ID: 100628
Name: Esophageal diverticulum
Synonym: Esophageal pouch
Definition: The presence of a diverticulum of the esophagus.
Comments:
Reference: HP:0100628
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute esophageal necrosis (HP:0011128) help
..expandEsophageal atresia (HP:0002032) help
..expandEsophageal duplication (HP:0100681) help
..expandEsophageal furrows (HP:0031858) help
..expandEsophageal leukoplakia (HP:0012859) help
..expandEsophageal neoplasm (HP:0100751) help
..expandEsophageal obstruction (HP:0005240) help
..expandEsophageal stenosis (HP:0010450) help
..expandEsophageal ulceration (HP:0004791) help
..expandEsophageal varix (HP:0002040) help
..expandEsophageal web (HP:0100594) help
..expandEsophagitis (HP:0100633) help
..expandSpontaneous esophageal perforation (HP:0005203) help
..expandTracheoesophageal fistula (HP:0002575) 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:0100628HP:0100628Esophageal diverticulum0INTU CL E G H2715229239OMIM:617925Short-Rib thoracic dysplasia 20 with polydactyly


Genes (1) :INTU

Diseases (1) :OMIM:617925
 

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