Cutaneous mucoepidermoid carcinoma

Summary

Cutaneous mucoepidermoid carcinoma (MONDO:0003091) is a cancer. A subtype of skin 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	cutaneous mucoepidermoid carcinoma
Mondo ID	MONDO:0003091
DOID	DOID:4683
NCIT	C4472
SNOMED CT	254713002
UMLS	C0346019
MedGen	91072
GARD	0023364
Anatomy (UBERON)	UBERON:0000014
Is cancer (heuristic)	yes

Also known as: zone of skin mucoepidermoid carcinoma

Disease family

This is a subtype of skin 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 body system or component › integumentary system disorder › integumentary system cancer › skin cancer › skin carcinoma › cutaneous mucoepidermoid carcinoma

Related subtypes (12): labia minora carcinoma, labia majora carcinoma, skin squamous cell carcinoma, cutaneous Paget disease, anal margin carcinoma, eyelid carcinoma, Borst-Jadassohn intraepidermal carcinoma, skin carcinoma in situ, skin basal cell carcinoma, vulvar seborrheic keratosis, skin appendage carcinoma, cutaneous neuroendocrine 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.