Necrotizing ulcerative gingivitis
diseaseOn this page
Also known as acute membranous gingivitisacute necrotising ulcerative gingivitis [ambiguous]acute necrotising ulcerative gingivostomatitis [ambiguous]ANUGFusospirillary gingivitisFusospirillosisphagedenic gingivitisVincent anginaVincent's anginaVincent's gingivitisVincent's infectionVincent's stomatitis
Summary
Necrotizing ulcerative gingivitis (MONDO:0006865) is a disease. A subtype of gingivitis — 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 | necrotizing ulcerative gingivitis |
| Mondo ID | MONDO:0006865 |
| EFO | EFO:1001058 |
| MeSH | D005892 |
| DOID | DOID:13924 |
| NCIT | C34637 |
| SNOMED CT | 186963008 |
| UMLS | C0017575 |
| MedGen | 42219 |
| Is cancer (heuristic) | no |
Also known as: acute membranous gingivitis · acute necrotising ulcerative gingivitis [ambiguous] · acute necrotising ulcerative gingivostomatitis [ambiguous] · ANUG · Fusospirillary gingivitis · Fusospirillosis · phagedenic gingivitis · Vincent angina · Vincent’s angina · Vincent’s gingivitis · Vincent’s infection · Vincent’s stomatitis
Disease family
This is a subtype of gingivitis. 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 › gingivitis › necrotizing ulcerative gingivitis
Related subtypes (1): chronic gingivitis
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.