Human Phenotype Ontology 
Grandparent Node:
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Abnormal esophagus morphology (HP:0002031)help
Grandparent Node:
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Neoplasm of head and neck (HP:0012288)help
Grandparent Node:
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Neoplasm of the gastrointestinal tract (HP:0007378)help
Parent Node:
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Esophageal neoplasm (HP:0100751)help
..Starting node
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Esophageal squamous papilloma (HP:0031463)help
Term ID: 31463
Name: Esophageal squamous papilloma
Synonym:
Definition: A rare benign epithelial tumor that is usually asymptomatic but can present with pyrosis and epigastric discomfort with or without dysphagia. Histopathologically, esophageal squamous papilloma has fingerlike projections lined with acanthotic stratified squamous epithelium with conservation of normal cellular with or without cellular atypia.
Comments:
Reference: HP:0031463
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBarrett esophagus (HP:0100580) help
..expandEsophageal carcinoma (HP:0011459) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031463HP:0031463Esophageal squamous papilloma0 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 August 2021 release.