Gallbladder papillary neoplasm with an associated invasive carcinoma

Summary

Gallbladder papillary neoplasm with an associated invasive carcinoma (MONDO:0004148) is a cancer. A subtype of papillary adenocarcinoma — 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	gallbladder papillary neoplasm with an associated invasive carcinoma
Mondo ID	MONDO:0004148
DOID	DOID:7221
NCIT	C5743
UMLS	C1333753
MedGen	232226
GARD	0023849
Anatomy (UBERON)	UBERON:0002110
Is cancer (heuristic)	yes

Also known as: gall bladder papillary carcinoma · gallbladder papillary neoplasm with an associated invasive cancer · gallbladder papillary neoplasm with an associated invasive carcinoma · intracystic papillary neoplasm with an associated invasive carcinoma · papillary carcinoma of gallbladder · papillary carcinoma of the gallbladder

Disease family

This is a subtype of papillary adenocarcinoma. 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 › carcinoma › adenocarcinoma › papillary adenocarcinoma › gallbladder papillary neoplasm with an associated invasive carcinoma

Related subtypes (10): papillary eccrine carcinoma, breast papillary carcinoma, papillary thymic adenocarcinoma, fallopian tube papillary adenocarcinoma, ovarian serous surface papillary adenocarcinoma, papillary cystadenocarcinoma, thyroid gland papillary carcinoma, papillary lung adenocarcinoma, gastric papillary adenocarcinoma, papillary renal cell 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.