round cell sarcoma with EWSR1-PATZ1 gene fusion

Summary

round cell sarcoma with EWSR1-PATZ1 gene fusion (MONDO:0958300) is a cancer. A subtype of round cell sarcoma with EWSR1-non-ETS fusion — 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	round cell sarcoma with EWSR1-PATZ1 gene fusion
Mondo ID	MONDO:0958300
DOID	DOID:0081409
UMLS	C5555053
MedGen	1791494
Is cancer (heuristic)	yes

Disease family

This is a subtype of round cell sarcoma with EWSR1-non-ETS fusion. 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 › sarcoma › small cell sarcoma › round cell sarcoma with EWSR1-non-ETS fusion › round cell sarcoma with EWSR1-PATZ1 gene fusion

Related subtypes (3): childhood round cell sarcoma with EWSR1-non-ETS fusion, round cell sarcoma with EWSR1-NFATC2 gene fusion, round cell sarcoma with FUS-NFATC2 gene fusion

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.