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 viral infections (HP:0004429)

Parent Node:
Recurrent herpes (HP:0005353)

..Starting node
..Recurrent oral herpes (HP:0410028)

Term ID:

410028

Name:

Recurrent oral herpes

Synonym:

Recurrent herpes labialis

Definition:

Recurrent episodes of oral herpes, typically characterized by blisters or ulcers on the gums, lips and/or tongue caused by herpes virus.

Comments:

Reference:

HP:0410028

Genes and Diseases:

Child Nodes:

Sister Nodes:

Herpes simplex encephalitis (HP:0012302)

Kaposi's sarcoma (HP:0100726)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410028	HP:0410028	Recurrent oral herpes	0	FCGR3A CL E G H	2214	3619	OMIM:615707	Immunodeficiency 20	4
HP:0410028	HP:0410028	Recurrent oral herpes	0	NFKB2 CL E G H	4791	7795	OMIM:615577	Immunodeficiency, common variable, 10	11
HP:0410028	HP:0410028	Recurrent oral herpes	0	REL CL E G H	5966	9954	OMIM:619652	IMMUNODEFICIENCY 92; IMD92	1
HP:0410028	HP:0410028	Recurrent oral herpes	0	TPP2 CL E G H	7174	12016	OMIM:619220	IMMUNODEFICIENCY 78 WITH AUTOIMMUNITY AND DEVELOPMENTAL DELAY; IMD78

Genes (4) :FCGR3A NFKB2 REL TPP2

Diseases (4) :OMIM:615707 OMIM:615577 OMIM:619652 OMIM:619220

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.