Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the head (HP:0000234)help
Parent Node:
expandAbnormality of the pharynx (HP:0000600)help
..Starting node
..expandHypoplasia of the pharynx (HP:0009555)help
Term ID: 9555
Name: Hypoplasia of the pharynx
Synonym: Decreased diameter of pharynx; Decreased length of pharynx; Decreased size of pharynx; Decreased volume of pharynx; Decreased width of pharynx; Hypotrophic pharynx; Small pharynx; Underdevelopment of pharynx
Definition: Underdevelopment of the pharynx.
Comments:
Reference: HP:0009555
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal hypopharynx morphology (HP:3000053) help
..expandAbnormal morphology of musculature of pharynx (HP:0430015) help
..expandAbnormal nasopharynx morphology (HP:0001739) 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:0009555HP:0009555Hypoplasia of the pharynx0TCOF1 CL E G H694911654OMIM:154500Treacher collins-franceschetti syndrome.140


Genes (1) :TCOF1

Diseases (1) :OMIM:154500
 

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