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:
Abnormality of the alveolar ridges (HP:0006477)

Parent Node:
Alveolar ridge overgrowth (HP:0009085)

..Starting node
..Thick anterior alveolar ridges (HP:0009100)

Term ID:

9100

Name:

Thick anterior alveolar ridges

Synonym:

Thick anterior alveolar process of jaw

Definition:

Comments:

Reference:

HP:0009100

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0009100	HP:0009100	Thick anterior alveolar ridges	0	CD96 CL E G H	10225	16892	OMIM:211750	C syndrome	.	83

Genes (1) :CD96

Diseases (1) :OMIM:211750

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