Human Phenotype Ontology 
Grandparent Node:
expandAbnormal hard palate morphology (HP:0100737)help
Grandparent Node:
expandOral cleft (HP:0000202)help
Parent Node:
expandCleft palate (HP:0000175)help
..Starting node
..expandCleft maxillary alveolus (HP:0410003)help
Term ID: 410003
Name: Cleft maxillary alveolus
Synonym: Alveolar cleft; Cleft alveolar process of maxilla; Cleft anterior maxilla; Cleft primary palate
Definition: Alveolar cleft is a tornado-shaped bone defect in the maxillary arch. Alveolar cleft occurs in response to divergence from normal development during frontonasal prominence growth, contact, and fusion. The most common alveolar portion of the cleft is located between the lateral incisor and the canine.
Comments:
Reference: HP:0410003
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMedian cleft palate (HP:0009099) help
..expandNon-midline cleft palate (HP:0100338) help
..expandobsolete Cleft secondary palate (HP:0410004) help
..expandSubmucous cleft of soft and hard palate (HP:0410031) 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:0410003HP:0410003Cleft maxillary alveolus0PUF60 CL E G H2282717042ORPHA:5084888q24.3 microdeletion syndromeHP:0040283 - Occasional19


Genes (1) :PUF60

Diseases (1) :ORPHA:508488
 

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