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:
Abnormal vascular morphology (HP:0025015)

Parent Node:
Vasculitis (HP:0002633)

..Starting node
..Nodular inflammatory vasculitis (HP:0005300)

Term ID:

5300

Name:

Nodular inflammatory vasculitis

Synonym:

Definition:

Comments:

Reference:

HP:0005300

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cerebral vasculitis (HP:0005318)

Inflammatory arteriopathy (HP:0005291)

Large vessel vasculitis (HP:0005310)

Small vessel vasculitis (HP:0011944)

Vasculitis in the skin (HP:0200029)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005300	HP:0005300	Nodular inflammatory vasculitis	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.