Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the premaxilla (HP:0010758)help
Parent Node:
expandAplasia of facial bones (HP:0040008)help
Parent Node:
expandAplasia/Hypoplasia of the premaxilla (HP:0010756)help
..Starting node
..expandAplasia of the premaxilla (HP:0010757)help
Term ID: 10757
Name: Aplasia of the premaxilla
Synonym: Absence of the intermaxillary bone; Absence of the premaxilla; Absence of the primary palate bone; Aplasia of the intermaxillary bone; Aplasia of the primary palate bone; Failure of development of premaxilla; Failure of development of the primary palate bone; Missing premaxilla; Missing primary palate bone
Definition: Absence of the premaxilla, which is the embryonic structure that forms the anterior part of the maxilla.
Comments:
Reference: HP:0010757
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHypoplasia of the premaxilla (HP:0010650) 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:0010757HP:0010757Aplasia of the premaxilla0SIX3 CL E G H649610889OMIM:157170Holoprosencephaly 232


Genes (1) :SIX3

Diseases (1) :OMIM:157170
 

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