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:
Recurrent infections (HP:0002719)

Parent Node:
Recurrent skin infections (HP:0001581)

Parent Node:
Recurrent viral infections (HP:0004429)

..Starting node
..Recurrent viral skin infections (HP:0011371)

Term ID:

11371

Name:

Recurrent viral skin infections

Synonym:

Recurrent viral skin infections

Definition:

Increased susceptibility to viral skin infections, as manifested by recurrent episodes of viral skin infections.

Comments:

Reference:

HP:0011371

Genes and Diseases:

Child Nodes:

Sister Nodes:

obsolete Severe viral infections (HP:0005364)

Recurrent enteroviral infections (HP:0002743)

Recurrent herpes (HP:0005353)

Severe recurrent varicella (HP:0005428)

Susceptibility to chickenpox (HP:0005360)

Susceptibility to coronavirus 229e (HP:0005396)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011371	HP:0011371	Recurrent viral skin infections	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.