Pancreas, dorsal, agenesis of
disease diseaseOn 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
| Field | Value |
|---|---|
| Canonical name | pancreas, dorsal, agenesis of |
| Mondo ID | MONDO:0008184 |
| MeSH | C538109 |
| OMIM | 167755 |
| UMLS | C1868659 |
| MedGen | 357024 |
| GARD | 0015104 |
| 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 disease › pancreatic agenesis › pancreas, 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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.