Duodenal somatostatinoma
disease diseaseOn this page
Also known as duodenal delta cell somatostatin producing tumourduodenal somatostatin producing tumorduodenal somatostatin producing tumourduodenal somatostatin-producing NETduodenal somatostatin-producing neuroendocrine tumorduodenal somatostatin-producing neuroendocrine tumour
Summary
Duodenal somatostatinoma (MONDO:0004236) is a disease. A subtype of duodenal neuroendocrine tumor, well differentiated, low or intermediate grade — 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 | duodenal somatostatinoma |
| Mondo ID | MONDO:0004236 |
| DOID | DOID:7479 |
| NCIT | C27407 |
| UMLS | C1333320 |
| MedGen | 234205 |
| GARD | 0023892 |
| Is cancer (heuristic) | no |
Also known as: duodenal delta cell somatostatin producing tumour · duodenal somatostatin producing tumor · duodenal somatostatin producing tumour · duodenal somatostatin-producing NET · duodenal somatostatin-producing neuroendocrine tumor · duodenal somatostatin-producing neuroendocrine tumour · duodenal somatostatinoma
Disease family
Classification path: disease › human disease › disease by body system or component › digestive system disorder › digestive system neuroendocrine neoplasm › digestive system neuroendocrine tumor, grade 1/2 › small intestine neuroendocrine tumor, well differentiated, low or intermediate grade › duodenal neuroendocrine tumor, well differentiated, low or intermediate grade › duodenal somatostatinoma
Related subtypes (1): duodenal gastrin-producing neuroendocrine tumor
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.