Spinal cord glioma

disease
On this page

Also known as glial neoplasm spinal cordglial tumor of spinal cordglial tumour of spinal cordmalignant glioma of spinal cordspinal cord glial neoplasmspinal cord glial tumorspinal cord glial tumourspinal cord malignant glioma

Summary

Spinal cord glioma (MONDO:0002542) is a cancer and 1 clinical trial. Top therapeutic interventions include onc-206. A subtype of spinal cord cancer — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namespinal cord glioma
Mondo IDMONDO:0002542
DOIDDOID:3185
NCITC4534
SNOMED CT254946004
UMLSC2937245
MedGen423646
GARD0023158
Anatomy (UBERON)UBERON:0002240
Is cancer (heuristic)yes

Also known as: glial neoplasm spinal cord · glial tumor of spinal cord · glial tumour of spinal cord · malignant glioma of spinal cord · spinal cord glial neoplasm · spinal cord glial tumor · spinal cord glial tumour · spinal cord glioma · spinal cord malignant glioma

Data availability: 1 cell line.

Disease family

This is a subtype of spinal cord 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 etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmcancernervous system cancercentral nervous system cancerspinal cord cancerspinal cord glioma

Related subtypes (7): spinal cord lymphoma, spinal cord melanoma, spinal cord sarcoma, spinal cord neuroblastoma, spinal meninges cancer, spinal cord primitive neuroectodermal tumor, metastatic malignant neoplasm in the spinal cord

Subtypes (4): spinal cord oligodendroglioma, spinal cord astrocytoma, adult spinal cord glioblastoma, ependymal tumor of spinal cord

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: 1.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04732065PHASE1RECRUITINGONC206 for Treatment of Newly Diagnosed, Recurrent Diffuse Midline Gliomas, and Other Recurrent Malignant CNS Tumors

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
ONC-20611

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