Spinal cord melanoma

Summary

Spinal cord melanoma (MONDO:0001893) is a cancer. 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 features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	spinal cord melanoma
Mondo ID	MONDO:0001893
DOID	DOID:14151
NCIT	C5158
UMLS	C1336045
MedGen	236837
GARD	0023031
Anatomy (UBERON)	UBERON:0002240
Is cancer (heuristic)	yes

Also known as: melanoma (disease) of spinal cord · melanoma of spinal cord · melanoma of the spinal cord · spinal cord melanoma · spinal cord melanoma (disease)

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 tumor › neoplastic disease or syndrome › neoplasm › cancer › nervous system cancer › central nervous system cancer › spinal cord cancer › spinal cord melanoma

Related subtypes (7): spinal cord lymphoma, spinal cord sarcoma, spinal cord glioma, spinal cord neuroblastoma, spinal meninges cancer, spinal cord primitive neuroectodermal tumor, metastatic malignant neoplasm in the 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: 0.