Bladder signet ring cell adenocarcinoma

Summary

Bladder signet ring cell adenocarcinoma (MONDO:0003891) is a disease. A subtype of bladder adenocarcinoma — 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	bladder signet ring cell adenocarcinoma
Mondo ID	MONDO:0003891
DOID	DOID:6481
NCIT	C6163
UMLS	C1332563
MedGen	231949
Anatomy (UBERON)	UBERON:0001255
Is cancer (heuristic)	no

Also known as: bladder signet ring cell adenocarcinoma · urinary bladder signet Ring adenocarcinoma · urinary bladder signet ring cell carcinoma

Disease family

This is a subtype of bladder 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 › bladder adenocarcinoma › bladder signet ring cell adenocarcinoma

Related subtypes (6): bladder colloid adenocarcinoma, bladder clear cell adenocarcinoma, bladder colonic type adenocarcinoma, bladder urachal adenocarcinoma, bladder mixed adenocarcinoma, bladder hepatoid adenocarcinoma

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.