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:
Abnormal palate morphology (HP:0000174)

..Starting node
..Palatal edema (HP:0031089)

Term ID:

31089

Name:

Palatal edema

Synonym:

Palatal oedema; Palate edema; Palate oedema

Definition:

Swelling related to fluid accumulation within the palate.

Comments:

Reference:

HP:0031089

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal hard palate morphology (HP:0100737)

Abnormal soft palate morphology (HP:0100736)

High palate (HP:0000218)

Narrow palate (HP:0000189)

Palate fistula (HP:0010294)

Palate telangiectasia (HP:0002707)

Prominent median palatal raphe (HP:0002708)

Prominent palatine ridges (HP:0010291)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031089	HP:0031089	Palatal edema	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.