Human Phenotype Ontology 
Grandparent Node:
expandAbnormal number of incisors (HP:0011064)help
Grandparent Node:
expandSelective tooth agenesis (HP:0001592)help
Parent Node:
expandAgenesis of incisor (HP:0006485)help
..Starting node
..expandAgenesis of mandibular incisor (HP:0200161)help
Term ID: 200161
Name: Agenesis of mandibular incisor
Synonym: Absence of lower front tooth; Absence of lower incisor; Absence of mandibular incisor; Agenesis of lower incisor; Failure of development of mandibular incisor; Missing lower front tooth; Missing lower incisor
Definition:
Comments:
Reference: HP:0200161
Genes and Diseases:
 
       Child Nodes:
........expandAgenesis of mandibular central incisor (HP:0006355) help
................... HP:0011047 Agenesis of primary mandibular central incisor
................... HP:0011048 Agenesis of permanent mandibular central incisor
........expandAgenesis of mandibular lateral incisor (HP:0200154) help
................... HP:0200158 Agenesis of permanent mandibular lateral incisor
................... HP:0200159 Agenesis of primary mandibular lateral incisor

 Sister Nodes: 
..expandAgenesis of central incisor (HP:0006289) help
..expandAgenesis of lateral incisor (HP:0200153) help
..expandAgenesis of maxillary incisor (HP:0200160) 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:0200161HP:0200161Agenesis of mandibular incisor0EIF4A3 CL E G H977518683OMIM:268305Robin sequence with cleft mandible and limb anomalies4
HP:0200161HP:0200154Agenesis of mandibular lateral incisor1 CL E G H
HP:0200161HP:0006355Agenesis of mandibular central incisor1EIF4A3 CL E G H977518683OMIM:268305Robin sequence with cleft mandible and limb anomalies.4
HP:0200161HP:0200159Agenesis of primary mandibular lateral incisor2 CL E G H
HP:0200161HP:0200158Agenesis of permanent mandibular lateral incisor2 CL E G H
HP:0200161HP:0011048Agenesis of permanent mandibular central incisor2 CL E G H
HP:0200161HP:0011047Agenesis of primary mandibular central incisor2 CL E G H


Genes (1) :EIF4A3

Diseases (1) :OMIM:268305
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.