Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Vascular skin abnormality (HP:0011276)

Parent Node:
Urticaria (HP:0001025)

..Starting node
..Chronic idiopathic urticaria (HP:0410133)

Term ID:

410133

Name:

Chronic idiopathic urticaria

Synonym:

Chronic spontaneous urticaria; CIU; CSU

Definition:

Urticaria characterized by spontaneously recurring hives for 6 weeks or longer.

Comments:

Reference:

HP:0410133

Genes and Diseases:

Child Nodes:

Sister Nodes:

Darier's sign (HP:0025081)

Dermatographic urticaria (HP:0011971)

Physical urticaria (HP:0410134)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410133	HP:0410133	Chronic idiopathic 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.