Human Phenotype Ontology 
Grandparent Node:
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Abnormal oral cavity morphology (HP:0000163)help
Parent Node:
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Abnormality of the alveolar ridges (HP:0006477)help
..Starting node
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Alveolar process hypoplasia (HP:0006329)help
Term ID: 6329
Name: Alveolar process hypoplasia
Synonym: Decreased size of alveolar process of jaw; Decreased size of alveolar ridge; Deficiency of alveolar process of jaw; Deficiency of alveolar ridge; Hypoplasia of alveolar ridge; Hypoplastic alveolar bone; Hypotrophic alveolar process of jaw; Hypotrophic alveolar ridge; Small alveolar process of jaw; Small alveolar ridge; Underdevelopment of alveolar process of jaw; Underdevelopment of alveolar ridge
Definition: Underdevelopment of the alveolar process (also known as alveolar bone).
Comments:
Reference: HP:0006329
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAlveolar ridge overgrowth (HP:0009085) help
..expandAtrophy of alveolar ridges (HP:0006308) help
..expandBroad alveolar ridges (HP:0000187) help
..expandFibrous syngnathia (HP:0009754) help
..expandMidline notch of upper alveolar ridge (HP:0009084) help
..expandProgressive alveolar ridge hypertropy (HP:0009092) 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:0006329HP:0006329Alveolar process hypoplasia0KIF7 CL E G H37465430497OMIM:200990Acrocallosal syndrome167


Genes (1) :KIF7

Diseases (1) :OMIM:200990
 

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