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:
Genital neoplasm (HP:0010787)

Parent Node:
Vulvar neoplasm (HP:0030416)

..Starting node
..Bartholin gland carcinoma (HP:0030419)

Term ID:

30419

Name:

Bartholin gland carcinoma

Synonym:

Definition:

A cancer arising in a cell of the Bartholin gland, a racemose gland located slightly posterior to the opening of the vagina.

Comments:

Reference:

HP:0030419

Genes and Diseases:

Child Nodes:

Sister Nodes:

Squamous cell carcinoma of the vulva (HP:0030417)

Vulvar adenocarcinoma (HP:0030420)

Vulvar melanoma (HP:0030418)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030419	HP:0030419	Bartholin gland carcinoma	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.