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 lip morphology (HP:0000159)

Parent Node:
Vascular malformation of the lip (HP:0031486)

..Starting node
..Venous malformation of the lip (HP:0031489)

Term ID:

31489

Name:

Venous malformation of the lip

Synonym:

Definition:

A vascular malformation located in the lip that is related to abnormal vascular morphogenesis.

Comments:

Reference:

HP:0031489

Genes and Diseases:

Child Nodes:

Sister Nodes:

Arteriovenous malformation of the lip (HP:0031488)

Capillary malformation of the lip (HP:0031487)

Hemangioma of the lip (HP:0031490)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031489	HP:0031489	Venous malformation of the lip	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.