Bronchus adenoma

Summary

Bronchus adenoma (MONDO:0003427) is a cancer. A subtype of papillary 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	bronchus adenoma
Mondo ID	MONDO:0003427
DOID	DOID:5391
NCIT	C3494
UMLS	C0149845
MedGen	56206
Anatomy (UBERON)	UBERON:0002185
Is cancer (heuristic)	yes

Also known as: adenoma of bronchus · adenoma of the bronchus · adenoma, bronchial, benign · bronchial adenoma · bronchial adenoma NOS (morphologic abnormality) · bronchus adenoma · lung papillary adenoma · papillary adenoma of type II pneumocytes · peripheral papillary tumor of type II pneumocytes · peripheral papillary tumour of type II pneumocytes · type II pneumocyte adenoma

Disease family

This is a subtype of papillary 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 › papillary adenoma › bronchus adenoma

Related subtypes (5): eccrine papillary adenoma, chromophil adenoma of the kidney, ovarian papillary cystadenoma, extrahepatic bile duct papillary adenoma, papillary cystadenoma

Subtypes (1): lung mucous gland adenoma

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.