Buschke Lowenstein tumor

Summary

Buschke Lowenstein tumor (MONDO:0027026) is a cancer. A subtype of reproductive system cancer — 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	Buschke Lowenstein tumor
Mondo ID	MONDO:0027026
MeSH	D062688
NCIT	C6371
SNOMED CT	402910001
UMLS	C0276264
MedGen	473018
GARD	0009663
Is cancer (heuristic)	yes

Also known as: anogenital type verrucous carcinoma · Buschke Lowenstein tumor · Buschke-Lowenstein tumor · Buschke-Lowenstein tumour · condyloma Acuminatum, Giant · condyloma Acuminatums, Giant · GCBL · Giant condyloma Acuminatum · giant condyloma acuminatum involving the prepuce and glans penis · Giant condyloma Acuminatums · Giant condyloma of Buschke and Lowenstein · giant condyloma of Buschke and Lowenstein · Lowenstein tumor, Buschke · tumor, Buschke Lowenstein · tumor, Buschke-Lowenstein

Disease family

This is a subtype of reproductive system cancer. 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 › cancer › reproductive system cancer › Buschke Lowenstein tumor

Related subtypes (7): malignant Leydig cell tumor, malignant Sertoli cell tumor, female reproductive organ cancer, prepuce cancer, pituitary cancer, male reproductive organ cancer, gonadoblastoma

Subtypes (1): anal verrucous carcinoma

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.