Human Phenotype Ontology 
Grandparent Node:
expandAgenesis of central incisor (HP:0006289)help
Grandparent Node:
expandAgenesis of maxillary incisor (HP:0200160)help
Parent Node:
expandAgenesis of maxillary central incisor (HP:0006293)help
..Starting node
..expandAgenesis of permanent maxillary central incisor (HP:0011045)help
Term ID: 11045
Name: Agenesis of permanent maxillary central incisor
Synonym: Absence of permanent maxillary central incisor; Absence of permanent upper central incisor; Absence of permanent upper front tooth; Agenesis of adult maxillary central incisor; Failure of development of permanent maxillary central incisor; Missing adult upper central incisor; Missing permanent maxillary central incisor; Missing permanent upper central incisor; Missing permanent upper front tooth
Definition: Agenesis of upper secondary incisor.
Comments:
Reference: HP:0011045
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgenesis of primary maxillary central incisor (HP:0011046) 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:0011045HP:0011045Agenesis of permanent maxillary central 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.