Human Phenotype Ontology 
Grandparent Node:
expandAgenesis of incisor (HP:0006485)help
Parent Node:
expandAgenesis of central incisor (HP:0006289)help
Parent Node:
expandAgenesis of maxillary incisor (HP:0200160)help
..Starting node
..expandAgenesis of maxillary central incisor (HP:0006293)help
Term ID: 6293
Name: Agenesis of maxillary central incisor
Synonym: Absence of maxillary central incisor; Failure of development of maxillary central incisor; Missing maxillary central incisor; Missing upper central incisor
Definition: Agenesis of upper secondary incisor or of upper central primary incisor.
Comments:
Reference: HP:0006293
Genes and Diseases:
 
       Child Nodes:
........expandAgenesis of permanent maxillary central incisor (HP:0011045) help
........expandAgenesis of primary maxillary central incisor (HP:0011046) help

 Sister Nodes: 
..expandAgenesis of maxillary lateral incisor (HP:0000690) 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:0006293HP:0006293Agenesis of maxillary central incisor0 CL E G H
HP:0006293HP:0011046Agenesis of primary maxillary central incisor1 CL E G H
HP:0006293HP:0011045Agenesis of permanent maxillary central incisor1 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.