Salivary gland small cell carcinoma
diseaseOn this page
Also known as anaplastic small cell carcinoma of salivary glandanaplastic small cell carcinoma of the salivary glandneuroendocrine carcinoma of salivary glandneuroendocrine carcinoma of the salivary glandsaliva-secreting gland small cell carcinomasalivary gland anaplastic small cell carcinomasmall cell carcinoma of saliva-secreting glandsmall cell salivary gland carcinoma
Summary
Salivary gland small cell carcinoma (MONDO:0006405) is a cancer. A subtype of small cell carcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | salivary gland small cell carcinoma |
| Mondo ID | MONDO:0006405 |
| EFO | EFO:1000519 |
| NCIT | C35703 |
| UMLS | C1335982 |
| MedGen | 234786 |
| GARD | 0024400 |
| Anatomy (UBERON) | UBERON:0001044 |
| Is cancer (heuristic) | yes |
Also known as: anaplastic small cell carcinoma of salivary gland · anaplastic small cell carcinoma of the salivary gland · neuroendocrine carcinoma of salivary gland · neuroendocrine carcinoma of the salivary gland · saliva-secreting gland small cell carcinoma · salivary gland anaplastic small cell carcinoma · salivary gland small cell carcinoma · small cell carcinoma of saliva-secreting gland · small cell salivary gland carcinoma
Disease family
This is a subtype of small cell carcinoma. 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 › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › carcinoma › neuroendocrine carcinoma › small cell carcinoma › salivary gland small cell carcinoma
Related subtypes (17): extrahepatic bile duct small cell adenocarcinoma, ovarian small cell carcinoma, colon small cell neuroendocrine carcinoma, urinary bladder small cell neuroendocrine carcinoma, esophageal small cell neuroendocrine carcinoma, ampulla of vater small cell neuroendocrine carcinoma, Bartholin gland small cell carcinoma, thymus small cell carcinoma, cervical small cell carcinoma, endometrial small cell carcinoma, gallbladder small cell neuroendocrine carcinoma, gastric small cell neuroendocrine carcinoma, laryngeal small cell carcinoma, pancreatic small cell neuroendocrine carcinoma, prostate small cell carcinoma, ureter small cell carcinoma, small cell lung carcinoma
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.