Epulis

Summary

Epulis (MONDO:0003396) is a disease and 1 clinical trial. A subtype of gingival overgrowth — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Clinical trials: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	epulis
Mondo ID	MONDO:0003396
DOID	DOID:5337
ICD-11	1849228776
NCIT	C3948
SNOMED CT	45676007
UMLS	C0266919
MedGen	82751
Anatomy (UBERON)	UBERON:0001828
Is cancer (heuristic)	no

Also known as: gingiva polyp · gingival polyp · gum polyp · polyp of gingiva · polyp of gum · polyp of the gingiva · polyp of the gum

Disease family

This is a subtype of gingival overgrowth. 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 overgrowth › epulis

Related subtypes (2): gingival hypertrophy, hereditary gingival fibromatosis

Subtypes (2): congenital epulis, gingival fibroepithelial polyp

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
NCT03829059	Not specified	ACTIVE_NOT_RECRUITING	Histological/ Immunohistological and Molecularpathological Types of Epulides and Central Giant Cell Lesions of the Jaws