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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Atrophy of alveolar ridges (HP:0006308)help
Term ID: 6308
Name: Atrophy of alveolar ridges
Synonym: Alveolar bone loss; Atrophy of alveolar margins; Atrophy of alveolar processes of jaw; Flattening of alveolar margin; Flattening of alveolar processes of jaw; Flattening of alveolar ridges; Flattening of gum ridges; Resorption of alveolar margins; Resorption of alveolar processes of jaw; Resorption of alveolar ridges; Shrinking of alveolar ridges; Shrinking of gum ridges
Definition:
Comments:
Reference: HP:0006308
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAlveolar process hypoplasia (HP:0006329) help
..expandAlveolar ridge overgrowth (HP:0009085) 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:0006308HP:0006308Atrophy of alveolar ridges0C1R CL E G H7151246ORPHA:75392Periodontal Ehlers-Danlos syndromeHP:0040282 - Frequent15
HP:0006308HP:0006308Atrophy of alveolar ridges0C1S CL E G H7161247ORPHA:75392Periodontal Ehlers-Danlos syndromeHP:0040282 - Frequent7
HP:0006308HP:0006308Atrophy of alveolar ridges0CTSC CL E G H10752528ORPHA:678Papillon-Lefèvre syndromeHP:0040281 - Very frequent50
HP:0006308HP:0006308Atrophy of alveolar ridges0CTSC CL E G H10752528OMIM:245000Papillon-Lefevre syndrome.50
HP:0006308HP:0006308Atrophy of alveolar ridges0ELANE CL E G H19913309ORPHA:2686Cyclic neutropeniaHP:0040283 - Occasional79
HP:0006308HP:0006308Atrophy of alveolar ridges0LYST CL E G H11301968ORPHA:167Chédiak-Higashi syndromeHP:0040283 - Occasional239


Genes (5) :C1R C1S CTSC ELANE LYST

Diseases (5) :ORPHA:75392 ORPHA:678 OMIM:245000 ORPHA:2686 ORPHA:167
 

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