Spinal accessory nerve neoplasm

disease

On this page

Also known as accessory nerve neoplasmaccessory XI nerve spinal component neoplasmaccessory XI nerve spinal component neoplasm (disease)accessory XI nerve spinal component tumoraccessory XI nerve spinal component tumoureleventh cranial nerve neoplasmeleventh cranial nerve neoplasmseleventh cranial nerve tumoreleventh cranial nerve tumorseleventh cranial nerve tumoureleventh cranial nerve tumoursneoplasm of accessory XI nerve spinal componentneoplasm of eleventh cranial nerveneoplasm of spinal accessory nerveneoplasm of the eleventh cranial nerveneoplasm of the spinal accessory nervespinal accessory nerve neoplasmsspinal accessory nerve tumorspinal accessory nerve tumors

Summary

Spinal accessory nerve neoplasm (MONDO:0002626) is a cancer. A subtype of cranial nerve 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	spinal accessory nerve neoplasm
Mondo ID	MONDO:0002626
DOID	DOID:337
NCIT	C5829
SNOMED CT	126977003
UMLS	C1263902
MedGen	266074
Anatomy (UBERON)	UBERON:0009674
Is cancer (heuristic)	yes

Also known as: accessory nerve neoplasm · accessory XI nerve spinal component neoplasm · accessory XI nerve spinal component neoplasm (disease) · accessory XI nerve spinal component tumor · accessory XI nerve spinal component tumour · eleventh cranial nerve neoplasm · eleventh cranial nerve neoplasms · eleventh cranial nerve tumor · eleventh cranial nerve tumors · eleventh cranial nerve tumour · eleventh cranial nerve tumours · neoplasm of accessory XI nerve spinal component · neoplasm of eleventh cranial nerve · neoplasm of spinal accessory nerve · neoplasm of the eleventh cranial nerve · neoplasm of the spinal accessory nerve · spinal accessory nerve neoplasm · spinal accessory nerve neoplasms · spinal accessory nerve tumor · spinal accessory nerve tumors (+15 more)

Disease family

This is a subtype of cranial nerve 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 › nervous system disorder › peripheral nervous system disorder › peripheral nervous system neoplasm › cranial nerve neoplasm › spinal accessory nerve neoplasm

Related subtypes (11): trigeminal nerve neoplasm, abducens nerve neoplasm, facial nerve neoplasm, malignant cranial nerve neoplasm, oculomotor nerve neoplasm, hypoglossal nerve neoplasm, glossopharyngeal nerve neoplasm, optic nerve neoplasm, trochlear nerve neoplasm, olfactory nerve neoplasm, vestibulocochlear nerve neoplasm

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.