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 vasculature (HP:0002597)

Grandparent Node:
Generalized abnormality of skin (HP:0011354)

Parent Node:
Vascular skin abnormality (HP:0011276)

..Starting node
..Non-pruritic urticaria (HP:0011137)

Term ID:

11137

Name:

Non-pruritic urticaria

Synonym:

Non-itchy hives

Definition:

Pale reddish slightly elevated papules and plaques of 0.5-3 cm in diameter and not accompanied by pruritus.

Comments:

Reference:

HP:0011137

Genes and Diseases:

Child Nodes:

Sister Nodes:

Angioedema (HP:0100665)

Angiokeratoma (HP:0001014)

Cutis marmorata (HP:0000965)

Erythema (HP:0010783)

Prominent superficial blood vessels (HP:0007394)

Subcutaneous hemorrhage (HP:0001933)

Telangiectasia (HP:0001009)

Urticaria (HP:0001025)

Vasculitis in the skin (HP:0200029)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011137	HP:0011137	Non-pruritic 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.