Gingival neoplasm
diseaseOn this page
Also known as gingiva neoplasmgingiva neoplasm (disease)gingiva tumorgingiva tumourgingival tumorgingival tumourgum neoplasmgum tumorgum tumourneoplasm of gingivaneoplasm of gumneoplasm of the gingivaneoplasm of the gumtumor of gingivatumor of gumtumor of the gingivatumor of the gumtumour of gingivatumour of gum
Summary
Gingival neoplasm (MONDO:0021086) is a cancer and 1 clinical trial. A subtype of gingival disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Clinical trials: 1
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | gingival neoplasm |
| Mondo ID | MONDO:0021086 |
| NCIT | C3057 |
| SNOMED CT | 126792007 |
| UMLS | C0017570 |
| MedGen | 6605 |
| Anatomy (UBERON) | UBERON:0001828 |
| Is cancer (heuristic) | yes |
Also known as: gingiva neoplasm · gingiva neoplasm (disease) · gingiva tumor · gingiva tumour · gingival neoplasm · gingival tumor · gingival tumour · gum neoplasm · gum tumor · gum tumour · neoplasm of gingiva · neoplasm of gum · neoplasm of the gingiva · neoplasm of the gum · tumor of gingiva · tumor of gum · tumor of the gingiva · tumor of the gum · tumour of gingiva · tumour of gum (+2 more)
Disease family
This is a subtype of gingival disorder. 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 › musculoskeletal system disorder › skeletal system disorder › periodontal disorder › gingival disorder › gingival neoplasm
Related subtypes (5): gingival recession, gingival overgrowth, gingivitis, pericoronitis, leukoplakia of gingiva
Subtypes (3): gingival cancer, congenital epulis, benign neoplasm of gum
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: 1.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03239834 | Not specified | COMPLETED | Clinical Evaluation of the OncAlert RAPID in Subjects Presenting for Evaluation and/or Initial Biopsy; Impact on Decision-Making |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.