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 web (HP:0100594)help
Term ID: 100594
Name: Esophageal web
Synonym:
Definition: Thin (2-3mm) membranes of normal esophageal tissue consisting of mucosa and submucosa that can be congenital or acquired. Congenital webs commonly appear in the middle and inferior third of the esophagus, and they are more likely to be circumferential with a central or eccentric orifice. Acquired webs are much more common than congenital webs and typically appear in the cervical area (postcricoid). Clinical symptoms of this condition are selective (solid more than liquids) dysphagia, thoracic pain, nasopharyngeal reflux, aspiration, perforation and food impaction (the last two are very rare).
Comments:
Reference: HP:0100594
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute esophageal necrosis (HP:0011128) help
..expandEsophageal atresia (HP:0002032) help
..expandEsophageal diverticulum (HP:0100628) 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
..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:0100594HP:0100594Esophageal web0 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.