Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the head (HP:0000234)help
Parent Node:
expandAbnormality of the pharynx (HP:0000600)help
..Starting node
..expandAbnormal hypopharynx morphology (HP:3000053)help
Term ID: 3000053
Name: Abnormal hypopharynx morphology
Synonym: Abnormality of hypopharynx; Abnormality of lower pharynx
Definition: A structural anomaly of the hypopharyx, which is the most inferior portion of the pharynx. The hypopharynx continues from the oropharynx at the pharyngoepiglottic fold superiorly and extends inferiorly to the level of the inferior aspect of the cricoid cartilage, which marks the beginning of the cervical esophagus.
Comments:
Reference: HP:3000053
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal morphology of musculature of pharynx (HP:0430015) help
..expandAbnormal nasopharynx morphology (HP:0001739) help
..expandHypoplasia of the pharynx (HP:0009555) help
..expandOral-pharyngeal dysphagia (HP:0200136) help
..expandPharyngeal edema (HP:0011855) help
..expandPharyngitis (HP:0025439) help
..expandPosterior pharyngeal cleft (HP:0006783) 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:3000053HP:3000053Abnormal hypopharynx morphology0 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.