Vaginal rhabdomyosarcoma

Summary

Vaginal rhabdomyosarcoma (MONDO:0016095) is a disease. A subtype of vagina sarcoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	vaginal rhabdomyosarcoma
Mondo ID	MONDO:0016095
Orphanet	206492
NCIT	C128080
SNOMED CT	766759009
UMLS	C4288035
MedGen	925567
GARD	0020348
Anatomy (UBERON)	UBERON:0000996
Is cancer (heuristic)	no

Also known as: rhabdomyosarcoma (disease) of vagina · vagina rhabdomyosarcoma · vagina rhabdomyosarcoma (disease) · vaginal rhabdomyosarcoma

Disease family

This is a subtype of vagina sarcoma. 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: human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › reproductive system cancer › female reproductive organ cancer › vaginal cancer › vagina sarcoma › vaginal rhabdomyosarcoma

Related subtypes (2): endometrioid stromal sarcoma of the vagina, vagina leiomyosarcoma

Subtypes (1): botryoid-type embryonal rhabdomyosarcoma of the vagina

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.