Duodenal villous adenoma

Summary

Duodenal villous adenoma (MONDO:0006187) is a cancer. A subtype of villous adenoma — 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	duodenal villous adenoma
Mondo ID	MONDO:0006187
EFO	EFO:1000225
DOID	DOID:0050927
NCIT	C5338
UMLS	C1333322
MedGen	232438
Anatomy (UBERON)	UBERON:0002114
Is cancer (heuristic)	yes

Also known as: duodenal villous adenoma · duodenum villous adenoma · villous adenoma of duodenum · villous adenoma of the duodenum · villous adenoma, duodenum

Disease family

This is a subtype of villous adenoma. 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 › epithelial neoplasm › adenoma › villous adenoma › duodenal villous adenoma

Related subtypes (5): urinary bladder villous adenoma, urethral villous adenoma, vaginal villous adenoma, rectal villous adenoma, villous adenoma of colon

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.