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 primary maxillary central incisor (HP:0011046)help
Term ID: 11046
Name: Agenesis of primary maxillary central incisor
Synonym: Absence of deciduous maxillary central incisor; Absence of primary maxillary central incisor; Absence of upper front baby tooth; Agenesis of deciduous maxillary central incisor; Failure of development of deciduous maxillary central incisor; Failure of development of primary maxillary central incisor; Missing deciduous maxillary central incisor; Missing primary maxillary central incisor; Missing upper front baby tooth; Missing upper front milk tooth
Definition: Agenesis of upper central primary incisor.
Comments:
Reference: HP:0011046
Genes and Diseases:
 
       Child Nodes:

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