Benign vaginal neoplasm

Summary

Benign vaginal neoplasm (MONDO:0000647) is a cancer. A subtype of benign female reproductive system neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	benign vaginal neoplasm
Mondo ID	MONDO:0000647
DOID	DOID:0060114
ICD-10-CM	D28.1
ICD-11	1489085710
NCIT	C3610
SNOMED CT	92473001
UMLS	C0154002
MedGen	57810
Anatomy (UBERON)	UBERON:0000996
Is cancer (heuristic)	yes

Also known as: benign neoplasm of the vagina · benign neoplasm of vagina · benign tumor of the vagina · benign tumor of vagina · benign tumour of the vagina · benign tumour of vagina · benign vaginal neoplasm · benign vaginal neoplasms · benign vaginal tumor · benign vaginal tumour · vagina benign neoplasm · vagina female reproductive organ benign neoplasm

Disease family

This is a subtype of benign female reproductive system neoplasm. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › benign neoplasm › benign reproductive system neoplasm › benign female reproductive system neoplasm › benign vaginal neoplasm

Related subtypes (6): uterine benign neoplasm, vulvar benign neoplasm, fallopian tube benign neoplasm, ovarian benign neoplasm, adenomyoma, adenofibroma

Subtypes (4): vaginal leiomyoma, vaginal mullerian papilloma, benign vaginal mixed epithelial and mesenchymal neoplasm, vaginal squamous papilloma

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.