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 venous morphology (HP:0002624)

Grandparent Node:
Prominent superficial blood vessels (HP:0007394)

Parent Node:
Prominent superficial veins (HP:0001015)

..Starting node
..Lateral venous anomaly (HP:0100885)

Term ID:

100885

Name:

Lateral venous anomaly

Synonym:

Lateral marginal vein of Servelle; Vein of servelle

Definition:

Persistence of the embryonic dorsal or sciatic vein system that normally should have involuted around the tenth to twelfth week of intrauterine life.

Comments:

Reference:

HP:0100885

Genes and Diseases:

Child Nodes:

Sister Nodes:

Dilated superficial abdominal veins (HP:0030168)

Prominent scalp veins (HP:0001043)

Prominent veins on trunk (HP:0007457)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100885	HP:0100885	Lateral venous anomaly	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.