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:
Abnormal venous morphology (HP:0002624)

..Starting node
..Venous stenosis (HP:0025491)

Term ID:

25491

Name:

Venous stenosis

Synonym:

Definition:

Narrowing of a vein due to intimal hyperplasia and fibrosis.

Comments:

Reference:

HP:0025491

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal facial vein morphology (HP:3000043)

Abnormal inferior thyroid vein morphology (HP:3000059)

Abnormal jugular vein morphology (HP:3000042)

Abnormal vena cava morphology (HP:0005345)

Arteriovenous fistulas of celiac and mesenteric vessels (HP:0002642)

Prominent superficial veins (HP:0001015)

Venous insufficiency (HP:0005293)

Venous malformation (HP:0012721)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025491	HP:0025491	Venous stenosis	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.