Mediastinal soft tissue cancer

Summary

Mediastinal soft tissue cancer (MONDO:0037743) is a cancer. A subtype of mediastinal mesenchymal 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	mediastinal soft tissue cancer
Mondo ID	MONDO:0037743
NCIT	C6642
UMLS	C1334599
MedGen	277335
GARD	0027957
Is cancer (heuristic)	yes

Also known as: malignant mediastinal mesenchymal tumor · malignant mediastinal mesenchymal tumour · malignant mediastinal soft tissue neoplasm · malignant mediastinal soft tissue tumor · malignant mediastinal soft tissue tumour · malignant soft tissue neoplasm of mediastinum · malignant soft tissue neoplasm of the mediastinum · malignant soft tissue tumor of mediastinum · malignant soft tissue tumor of the mediastinum · malignant soft tissue tumour of mediastinum · malignant soft tissue tumour of the mediastinum · mediastinal mesenchymal tumor, malignant

Disease family

This is a subtype of mediastinal mesenchymal 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › connective and soft tissue neoplasm › soft tissue neoplasm › mediastinal mesenchymal tumor › mediastinal soft tissue cancer

Subtypes (1): mediastinum 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.