Lung leiomyosarcoma

disease
On this page

Also known as leiomyosarcoma of lungleiomyosarcoma of the lungpulmonary leiomyosarcoma

Summary

Lung leiomyosarcoma (MONDO:0003357) is a disease. A subtype of lung 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

FieldValue
Canonical namelung leiomyosarcoma
Mondo IDMONDO:0003357
DOIDDOID:5265
NCITC5667
UMLSC1334448
MedGen232711
GARD0023472
Anatomy (UBERON)UBERON:0002048
Is cancer (heuristic)no

Also known as: leiomyosarcoma of lung · leiomyosarcoma of the lung · lung leiomyosarcoma · pulmonary leiomyosarcoma

Data availability: 1 cell line.

Disease family

This is a subtype of lung 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 tumorneoplastic disease or syndromeneoplasmcancerrespiratory system cancerlung cancerlung sarcomalung leiomyosarcoma

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.