Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of premolar (HP:0011076)help
Grandparent Node:
expandSelective tooth agenesis (HP:0001592)help
Parent Node:
expandAgenesis of premolar (HP:0011051)help
..Starting node
..expandAgenesis of maxillary premolar (HP:0011052)help
Term ID: 11052
Name: Agenesis of maxillary premolar
Synonym: Absence of maxillary bicuspid; Absence of maxillary premolar; Absence of upper premolar; Agenesis of maxillary bicuspid; Failure of development of maxillary bicuspid; Failure of development of maxillary premolar; Missing maxillary premolar; Missing upper bicuspid; Missing upper premolar
Definition: Agenesis of maxillary premolar.
Comments:
Reference: HP:0011052
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgenesis of mandibular premolar (HP:0011053) 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:0011052HP:0011052Agenesis of maxillary premolar0 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.