Breast fibrosarcoma

Summary

Breast fibrosarcoma (MONDO:0003728) is a disease. A subtype of breast sarcoma — 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	breast fibrosarcoma
Mondo ID	MONDO:0003728
DOID	DOID:6001
NCIT	C5185
UMLS	C1332630
MedGen	272385
GARD	0023634
Anatomy (UBERON)	UBERON:0000310
Is cancer (heuristic)	no

Also known as: breast fibrosarcoma · breast fibrosarcoma (disease) · fibrosarcoma of breast · fibrosarcoma of the breast

Disease family

This is a subtype of breast sarcoma. 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › thoracic cancer › breast cancer › breast sarcoma › breast fibrosarcoma

Related subtypes (6): breast rhabdomyosarcoma, breast angiosarcoma, breast leiomyosarcoma, breast liposarcoma, breast extraskeletal osteosarcoma, breast synovial sarcoma

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.