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:
Urticaria (HP:0001025)

Parent Node:
Physical urticaria (HP:0410134)

..Starting node
..Vibratory urticaria (HP:0410138)

Term ID:

410138

Name:

Vibratory urticaria

Synonym:

Definition:

Urticaria in response to dermal vibration, with coincident degranulation of mast cells and increased histamine levels in serum.

Comments:

Reference:

HP:0410138

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aquagenic urticaria (HP:0410136)

Cold urticaria (HP:0410135)

Solar urticaria (HP:0410137)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410138	HP:0410138	Vibratory urticaria	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.