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:
Inflammatory abnormality of the skin (HP:0011123)

Parent Node:
Skin rash (HP:0000988)

..Starting node
..Bull's eye rash (HP:0040325)

Term ID:

40325

Name:

Bull's eye rash

Synonym:

Definition:

A cutaneous eruption that consists of multiple (at least two) concentric erythematous rings.

Comments:

Reference:

HP:0040325

Genes and Diseases:

Child Nodes:

Sister Nodes:

Discoid lupus rash (HP:0007417)

Heliotrope rash (HP:0040324)

Maculopapular exanthema (HP:0040186)

Malar rash (HP:0025300)

Morbilliform rash (HP:0012282)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040325	HP:0040325	Bull's eye rash	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.