Pancreas, dorsal, agenesis of

disease
On this page

Also known as agenesis of the dorsal pancreascomplete agenesis of the dorsal pancreascongenital short pancreaspancreas agenesis, dorsalpartial agenesis of the dorsal pancreas

Summary

Pancreas, dorsal, agenesis of (MONDO:0008184) is a disease. A subtype of pancreatic agenesis — 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

FieldValue
Canonical namepancreas, dorsal, agenesis of
Mondo IDMONDO:0008184
MeSHC538109
OMIM167755
UMLSC1868659
MedGen357024
GARD0015104
Is cancer (heuristic)no

Also known as: agenesis of the dorsal pancreas · complete agenesis of the dorsal pancreas · congenital short pancreas · pancreas agenesis, dorsal · pancreas, dorsal, agenesis of · partial agenesis of the dorsal pancreas

Disease family

This is a subtype of pancreatic agenesis. 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 › disease of genetic or genomic mechanism › hereditary diseasepancreatic agenesispancreas, dorsal, agenesis of

Related subtypes (3): pancreatic agenesis 2, pancreatic agenesis 1, pancreatic agenesis 3

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.

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