Gastric neuroendocrine tumor, well differentiated, low or intermediate grade
diseaseOn this page
Also known as gastric NETgastric NET G1/2gastric neuroendocrine tumorgastric neuroendocrine tumourgastric well differentiated endocrine tumorgastric well differentiated endocrine tumor/carcinomagastric well differentiated endocrine tumourGNETwell-differentiated neuroendocrine tumors of the stomachwell-differentiated neuroendocrine tumours of the stomach
Summary
Gastric neuroendocrine tumor, well differentiated, low or intermediate grade (MONDO:0015062) is a cancer (an umbrella term covering 5 Mondo subtypes) and 2 clinical trials. Top therapeutic interventions include octreotide and ribociclib. A subtype of digestive system neuroendocrine tumor, grade 1/2 — 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
| Field | Value |
|---|---|
| Canonical name | gastric neuroendocrine tumor, well differentiated, low or intermediate grade |
| Mondo ID | MONDO:0015062 |
| NCIT | C95871 |
| UMLS | C3272399 |
| MedGen | 474032 |
| GARD | 0025056 |
| Anatomy (UBERON) | UBERON:0000945 |
| Is cancer (heuristic) | yes |
Also known as: gastric NET · gastric NET G1/2 · gastric neuroendocrine tumor · gastric neuroendocrine tumour · gastric well differentiated endocrine tumor · gastric well differentiated endocrine tumor/carcinoma · gastric well differentiated endocrine tumour · GNET · well-differentiated neuroendocrine tumors of the stomach · well-differentiated neuroendocrine tumours of the stomach
Disease family
This is a subtype of digestive system neuroendocrine tumor, grade 1/2. 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 disorder › digestive system neuroendocrine neoplasm › digestive system neuroendocrine tumor, grade 1/2 › gastric neuroendocrine tumor, well differentiated, low or intermediate grade
Related subtypes (9): small intestine neuroendocrine tumor, well differentiated, low or intermediate grade, gastrin-producing neuroendocrine tumor, esophageal neuroendocrine tumor, L-cell glucagon-like peptide-producing neuroendocrine tumor, neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor, rectal neuroendocrine tumor, gallbladder neuroendocrine tumor, grade 1/2, pancreatic neuroendocrine tumor, intestinal neuroendocrine tumor G1
Subtypes (5): gastric gastrin-producing neuroendocrine tumor, gastric neuroendocrine tumor G1, familial gastric type 1 neuroendocrine tumor, gastric enterochromaffin cell serotonin-producing neuroendocrine tumor, gastric neuroendocrine tumor G2
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)
| Phase | Trials |
|---|---|
| PHASE2 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02420691 | PHASE2 | COMPLETED | Ribociclib in Treating Patients With Advanced Neuroendocrine Tumors of Foregut Origin |
| NCT03812939 | Not specified | UNKNOWN | Recurrence Rates of Type I Gastric Neuroendocrine Tumors Treated With Long-acting Somatostatin Analogs |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| OCTREOTIDE | 4 | 1 |
| RIBOCICLIB | 4 | 1 |
| CHEMBL3350037 | 0 | 1 |
Related Atlas pages
- Drugs: Octreotide, Ribociclib