Human Phenotype Ontology 
Grandparent Node:
expandAgenesis of lateral incisor (HP:0200153)help
Grandparent Node:
expandAgenesis of maxillary incisor (HP:0200160)help
Parent Node:
expandAgenesis of maxillary lateral incisor (HP:0000690)help
..Starting node
..expandAgenesis of permanent maxillary lateral incisor (HP:0011050)help
Term ID: 11050
Name: Agenesis of permanent maxillary lateral incisor
Synonym: Absence of permanent maxillary lateral incisor; Agenesis of permanent upper lateral incisor; Failure of development of permanent maxillary lateral incisor; Failure of development of permanent upper lateral incisor; Missing permanent maxillary lateral incisor; Missing permanent upper lateral incisor
Definition: Agenesis of one or more upper lateral secondary incisor.
Comments:
Reference: HP:0011050
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgenesis of primary maxillary lateral incisor (HP:0011049) 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:0011050HP:0011050Agenesis of permanent maxillary lateral incisor0 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.