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

..Starting node
..EBV encephalitis (HP:0033509)

Term ID:

33509

Name:

EBV encephalitis

Synonym:

Epstein-Barr virus encephalitis

Definition:

Inflamation of the brain related to infection by Epstein-Barr virus.

Comments:

Reference:

HP:0033509

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0033509	HP:0033509	EBV encephalitis	0	CD27 CL E G H	939	11922	OMIM:615122	Lymphoproliferative syndrome 2	4

Genes (1) :CD27

Diseases (1) :OMIM:615122

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