Combined small cell lung carcinoma

Summary

Combined small cell lung carcinoma (MONDO:0003438) is a cancer. A subtype of combined lung carcinoma — 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	combined small cell lung carcinoma
Mondo ID	MONDO:0003438
DOID	DOID:5421
ICD-11	392248394
NCIT	C9137
UMLS	C1333125
MedGen	234167
GARD	0023510
Is cancer (heuristic)	yes

Also known as: combined small and large cell lung cancer · combined small and large cell lung carcinoma · combined small cell and large cell lung carcinoma · combined small cell carcinoma of lung · combined small cell carcinoma of the lung · combined small cell lung cancer · combined small cell lung carcinoma · combined type small cell carcinoma of lung · combined type small cell carcinoma of the lung · combined type small cell lung carcinoma · CSCLC · mixed small cell and large cell carcinoma of lung · mixed small cell and large cell carcinoma of the lung · mixed small cell and large cell lung carcinoma · small cell and large cell carcinoma of lung · small cell and large cell carcinoma of the lung · small cell and large cell lung carcinoma

Disease family

This is a subtype of combined lung carcinoma. 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 › carcinoma › neuroendocrine carcinoma › combined lung carcinoma › combined small cell lung carcinoma

Related subtypes (1): lung combined large cell neuroendocrine carcinoma

Subtypes (1): lung combined type small cell adenocarcinoma

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.