Intradural extramedullary spinal canal neoplasm

disease
On this page

Also known as intradural extramedullary neoplasm of spinal canalintradural extramedullary neoplasm of the spinal canalintradural extramedullary spinal canal tumorintradural extramedullary spinal canal tumorsintradural extramedullary spinal canal tumourintradural extramedullary spinal canal tumoursintradural extramedullary spinal neoplasmsintradural extramedullary spinal tumoursintradural extramedullary tumor of spinal canalintradural extramedullary tumor of the spinal canalintradural extramedullary tumour of spinal canalintradural extramedullary tumour of the spinal canal

Summary

Intradural extramedullary spinal canal neoplasm (MONDO:0003545) is a cancer. A subtype of epidural spinal canal 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

FieldValue
Canonical nameintradural extramedullary spinal canal neoplasm
Mondo IDMONDO:0003545
DOIDDOID:5615
NCITC5135
UMLSC1334255
MedGen272771
Is cancer (heuristic)yes

Also known as: intradural extramedullary neoplasm of spinal canal · intradural extramedullary neoplasm of the spinal canal · intradural extramedullary spinal canal neoplasm · intradural extramedullary spinal canal tumor · intradural extramedullary spinal canal tumors · intradural extramedullary spinal canal tumour · intradural extramedullary spinal canal tumours · intradural extramedullary spinal neoplasms · intradural extramedullary spinal tumours · intradural extramedullary tumor of spinal canal · intradural extramedullary tumor of the spinal canal · intradural extramedullary tumour of spinal canal · intradural extramedullary tumour of the spinal canal

Disease family

This is a subtype of epidural spinal canal 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 body system or component › musculoskeletal system disorderskeletal system disordervertebral column disorderepidural spinal canal neoplasmintradural extramedullary spinal canal neoplasm

Related subtypes (1): epidural spinal canal angiolipoma

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.

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