Breast granular cell tumor

Summary

Breast granular cell tumor (MONDO:0002487) is a cancer. A subtype of granular cell tumor — 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	breast granular cell tumor
Mondo ID	MONDO:0002487
DOID	DOID:3011
NCIT	C40400
UMLS	C1511312
MedGen	307309
GARD	0023147
Anatomy (UBERON)	UBERON:0000310
Is cancer (heuristic)	yes

Also known as: breast granular cell tumor · granular cell tumor of breast · granular cell tumour of breast

Disease family

This is a subtype of granular cell tumor. 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 › nervous system disorder › peripheral nervous system disorder › peripheral nervous system neoplasm › nerve sheath neoplasm › granular cell tumor › breast granular cell tumor

Related subtypes (8): cutaneous granular cell tumor, benign granular cell tumor, esophageal granular cell tumor, granular cell cancer, vulvar granular cell tumor, mediastinal granular cell myoblastoma, neurohypophysis granular cell tumor, congenital epulis

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.