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:
Venous insufficiency (HP:0005293)

Parent Node:
Abnormality of female external genitalia (HP:0000055)

Parent Node:
Varicose veins (HP:0002619)

..Starting node
..Vulval varicose vein (HP:0100677)

Term ID:

100677

Name:

Vulval varicose vein

Synonym:

Definition:

Varicosity of veins in the vulval region.

Comments:

Reference:

HP:0100677

Genes and Diseases:

Child Nodes:

Sister Nodes:

Venous varicosities of celiac and mesenteric vessels (HP:0002626)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100677	HP:0100677	Vulval varicose vein	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.