Pancreatic exocrine neoplasm

disease
On this page

Also known as exocrine pancreas neoplasmexocrine pancreas neoplasm (disease)exocrine pancreas tumorexocrine pancreas tumourneoplasm of exocrine pancreasneoplasm of the exocrine pancreaspancreatic exocrine tumorpancreatic exocrine tumourtumor of exocrine pancreastumor of the exocrine pancreastumour of exocrine pancreastumour of the exocrine pancreas

Summary

Pancreatic exocrine neoplasm (MONDO:0021076) is a cancer (an umbrella term covering 5 Mondo subtypes) and 2 clinical trials. A subtype of pancreatic neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Umbrella term: 5 Mondo subtypes
  • Clinical trials: 2

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namepancreatic exocrine neoplasm
Mondo IDMONDO:0021076
NCITC4445
SNOMED CT254604005
UMLSC0345920
MedGen138030
Anatomy (UBERON)UBERON:0000017
Is cancer (heuristic)yes

Also known as: exocrine pancreas neoplasm · exocrine pancreas neoplasm (disease) · exocrine pancreas tumor · exocrine pancreas tumour · neoplasm of exocrine pancreas · neoplasm of the exocrine pancreas · pancreatic exocrine neoplasm · pancreatic exocrine tumor · pancreatic exocrine tumour · tumor of exocrine pancreas · tumor of the exocrine pancreas · tumour of exocrine pancreas · tumour of the exocrine pancreas

Disease family

This is a subtype of pancreatic neoplasm. 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 body system or component › digestive system disorderpancreas disorderpancreatic neoplasmpancreatic exocrine neoplasm

Related subtypes (6): pancreatic neuroendocrine neoplasm, malignant pancreatic neoplasm, GCGR-related hyperglucagonemia, adenoma of pancreas, benign neoplasm of pancreas, intraductal tubulopapillary neoplasm of pancreas

Subtypes (5): malignant exocrine pancreas neoplasm, pancreatic cystadenoma, pancreatic serous cystic neoplasm, benign neoplasm of exocrine pancreas, cystic tumor of the pancreas

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: 2.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified2

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06422455Not specifiedRECRUITINGAccess to Genetic Testing in Underserved Patients With Cancer
NCT01412684Not specifiedWITHDRAWNDistal Pancreatectomy With Partial Splenectomy for Pancreatic Tumors

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.