Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the maxilla (HP:0000326)help
Parent Node:
expandAbnormality of the premaxilla (HP:0010758)help
..Starting node
..expandHyperplasia of the premaxilla (HP:0430029)help
Term ID: 430029
Name: Hyperplasia of the premaxilla
Synonym: Hyperplasia of the intermaxillary bone; Hyperplasia of the primary palate bone; Increased size of premaxilla; Increased size of the primary palate bone; Large premaxilla; Large primary palate bone; Premaxillary excess; Primary palate bone excess
Definition: An abnormality of the premaxilla (the embryonic structure that forms the anterior part of the maxilla) causing it to appear relatively large in size compared to the other parts of the maxilla or other facial structures.
Comments:
Reference: HP:0430029
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/Hypoplasia of the premaxilla (HP:0010756) help
..expandProminence of the premaxilla (HP:0010759) 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:0430029HP:0430029Hyperplasia of the premaxilla0 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.