Spinal cord intramedullary teratoma

Summary

Spinal cord intramedullary teratoma (MONDO:0002717) is a disease. A subtype of central nervous system teratoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	spinal cord intramedullary teratoma
Mondo ID	MONDO:0002717
DOID	DOID:3639
NCIT	C5428
UMLS	C1334259
MedGen	233575
GARD	0023220
Is cancer (heuristic)	no

Also known as: intramedullary spinal cord teratoma · intramedullary spinal teratoma · intramedullary teratoma of spinal cord · intramedullary teratoma of the spinal cord

Disease family

This is a subtype of central nervous system teratoma. 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 › germ cell tumor › nongerminomatous germ cell tumor › teratoma › central nervous system teratoma › spinal cord intramedullary teratoma

Related subtypes (5): adult central nervous system teratoma, central nervous system mature teratoma, central nervous system immature teratoma, pineal region teratoma, spinal cord dermoid cyst

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.