Small intestinal sarcoma

Summary

Small intestinal sarcoma (MONDO:0003361) is a cancer. A subtype of small intestine cancer — 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	small intestinal sarcoma
Mondo ID	MONDO:0003361
DOID	DOID:5272
NCIT	C5335
UMLS	C1336007
MedGen	233455
GARD	0023475
Anatomy (UBERON)	UBERON:0002108
Is cancer (heuristic)	yes

Also known as: sarcoma of small bowel · sarcoma of small intestine · sarcoma of the small bowel · sarcoma of the small intestine · sarcoma, small intestinal · small bowel sarcoma · small intestinal sarcoma · small intestine sarcoma

Disease family

This is a subtype of small intestine cancer. 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 body system or component › digestive system disorder › intestinal disorder › intestinal neoplasm › small intestine neoplasm › small intestine cancer › small intestinal sarcoma

Related subtypes (5): duodenum cancer, ileum cancer, small intestine lymphoma, small intestine carcinoma, jejunal cancer

Subtypes (2): small intestine leiomyosarcoma, small intestinal fibrosarcoma

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.