Urinary bladder inverted papilloma

Summary

Urinary bladder inverted papilloma (MONDO:0004040) is a disease. A subtype of inverted urothelial papilloma — 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	urinary bladder inverted papilloma
Mondo ID	MONDO:0004040
DOID	DOID:6932
NCIT	C39859
SNOMED CT	447765004
UMLS	C1511190
MedGen	267740
Anatomy (UBERON)	UBERON:0001255
Is cancer (heuristic)	no

Also known as: bladder inverted papilloma · urinary bladder inverted papilloma

Disease family

This is a subtype of inverted urothelial papilloma. 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 by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › epithelial neoplasm › papillary epithelial neoplasm › papilloma › inverted papilloma › inverted transitional cell papilloma › inverted urothelial papilloma › urinary bladder inverted papilloma

Related subtypes (3): renal pelvis inverted papilloma, urethra inverted papilloma, ureter inverted 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.