Benign neoplasm of minor salivary gland

Summary

Benign neoplasm of minor salivary gland (MONDO:0021493) is a cancer. A subtype of neoplasm of minor salivary gland — 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	benign neoplasm of minor salivary gland
Mondo ID	MONDO:0021493
NCIT	C4411
SNOMED CT	92220004
UMLS	C0345615
MedGen	87508
Anatomy (UBERON)	UBERON:0001830
Is cancer (heuristic)	yes

Also known as: benign minor salivary gland neoplasm · benign minor salivary gland tumor · benign minor salivary gland tumour · benign neoplasm of the minor salivary gland · benign tumor of minor salivary gland · benign tumor of the minor salivary gland · benign tumour of minor salivary gland · benign tumour of the minor salivary gland · minor salivary gland benign neoplasm

Disease family

This is a subtype of neoplasm of minor salivary gland. 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 › mouth disorder › salivary gland disorder › tumor of salivary gland › neoplasm of minor salivary gland › benign neoplasm of minor salivary gland

Related subtypes (1): malignant tumor of minor salivary gland

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.