Human Phenotype Ontology 
Grandparent Node:
expandCleft hard palate (HP:0410005)help
Parent Node:
expandCleft of alveolar ridge of maxilla (HP:0010289)help
..Starting node
..expandCleft lower alveolar ridge (HP:0009094)help
Term ID: 9094
Name: Cleft lower alveolar ridge
Synonym: Cleft of lower alveolar process; Cleft of lower gingiva; Cleft of lower gum ridge; Cleft of mandibular alveolar process; Cleft of mandibular gingiva; Notch of lower alveolar process; Notch of lower alveolar ridge; Notch of lower gum ridge; Notch of mandibular alveolar process; Notch of mandibular alveolar ridge
Definition:
Comments:
Reference: HP:0009094
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBilateral alveolar cleft of maxilla (HP:0410034) help
..expandUnilateral alveolar cleft of maxilla (HP:0410033) 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:0009094HP:0009094Cleft lower alveolar ridge0EIF4A3 CL E G H977518683OMIM:268305Robin sequence with cleft mandible and limb anomalies.4


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.