Benign neoplasm of spinal cord

Summary

Benign neoplasm of spinal cord (MONDO:0021506) is a cancer. A subtype of central nervous system organ benign neoplasm — 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	benign neoplasm of spinal cord
Mondo ID	MONDO:0021506
ICD-10-CM	D33.4
ICD-11	1588169218
NCIT	C3627
SNOMED CT	92405007
UMLS	C0154034
MedGen	56329
Anatomy (UBERON)	UBERON:0002240
Is cancer (heuristic)	yes

Also known as: benign neoplasm of the spinal cord · benign spinal cord neoplasm · benign spinal cord tumor · benign spinal cord tumour · benign tumor of spinal cord · benign tumor of the spinal cord · benign tumour of spinal cord · benign tumour of the spinal cord · spinal cord benign neoplasm · spinal cord neoplasm, benign

Disease family

This is a subtype of central nervous system organ benign neoplasm. 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 › benign neoplasm › nervous system benign neoplasm › central nervous system organ benign neoplasm › benign neoplasm of spinal cord

Related subtypes (12): central nervous system chondroma, central nervous system hemangioma, central nervous system leiomyoma, central nervous system lipoma, craniopharyngioma, benign neoplasm of brain, benign neoplasm of meninges, benign neoplasm of peripheral nervous system, myxoid glioneuronal tumor, diffuse leptomeningeal glioneuronal tumor, multinodular and vacuolating neuronal tumor, polymorphous low grade neuroepithelial tumor of the young

Subtypes (2): spinal cord lipoma, spinal cord intramedullary teratoma

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.