Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal oral cavity morphology (HP:0000163)

Parent Node:
Abnormality of the alveolar ridges (HP:0006477)

..Starting node
..Progressive alveolar ridge hypertropy (HP:0009092)

Term ID:

9092

Name:

Progressive alveolar ridge hypertropy

Synonym:

Increasing overgrowth of gum ridge; Increasing size of gum ridge; Progressive hypertrophy of alveolar process of jaw

Definition:

Comments:

Reference:

HP:0009092

Genes and Diseases:

Child Nodes:

Sister Nodes:

Alveolar process hypoplasia (HP:0006329)

Alveolar ridge overgrowth (HP:0009085)

Atrophy of alveolar ridges (HP:0006308)

Broad alveolar ridges (HP:0000187)

Fibrous syngnathia (HP:0009754)

Midline notch of upper alveolar ridge (HP:0009084)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009092	HP:0009092	Progressive alveolar ridge hypertropy	0	GNPTAB CL E G H	79158	29670	OMIM:252500	Mucolipidosis II alpha/beta	.	240

Genes (1) :GNPTAB

Diseases (1) :OMIM:252500

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