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 mucosa morphology (HP:0011830)

Parent Node:
Abnormality of the gingiva (HP:0000168)

..Starting node
..Fusion of gums (HP:0012292)

Term ID:

12292

Name:

Fusion of gums

Synonym:

Fusion of gums; Fusion of the gingiva; Gingival synechia; Partial fusion of the gums; Synechia of the gums; Upper and lower gums fused together

Definition:

A congenital defect with an abnormal joining of the gums of the upper and lower jaw.

Comments:

Reference:

HP:0012292

Genes and Diseases:

Child Nodes:

Sister Nodes:

Gingival bleeding (HP:0000225)

Gingival calcification (HP:0025141)

Gingival cleft (HP:0030690)

Gingival fibromatosis (HP:0000169)

Gingival hyperkeratosis (HP:0000222)

Gingival overgrowth (HP:0000212)

Gingival recession (HP:0030816)

Gingivitis (HP:0000230)

Periodontitis (HP:0000704)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012292	HP:0012292	Fusion of gums	0	CL E G H

Genes (0) :

Diseases (0) :

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