Cranial nerve neoplasm

Summary

Cranial nerve neoplasm (MONDO:0002633) is a cancer (an umbrella term covering 12 Mondo subtypes). A subtype of peripheral nervous system neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer
• Umbrella term: 12 Mondo subtypes

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	cranial nerve neoplasm
Mondo ID	MONDO:0002633
MeSH	D003390
DOID	DOID:338
NCIT	C2963
SNOMED CT	126966009
UMLS	C0010267
MedGen	3263
Anatomy (UBERON)	UBERON:0001785
Is cancer (heuristic)	yes

Also known as: cranial nerve neoplasm · cranial nerve neoplasm (disease) · cranial nerve neoplasms · cranial nerve tumor · cranial nerve tumour · neoplasm of cranial nerve · neoplasm of the cranial nerve · tumor of cranial nerve · tumor of the cranial nerve · tumour of cranial nerve · tumour of the cranial nerve

Disease family

This is a subtype of peripheral nervous system 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

Related subtypes (8): autonomic nervous system neoplasm, nerve sheath neoplasm, mediastinal neural neoplasm, nerve plexus neoplasm, nerve root neoplasm, peripheral ganglioneuroblastoma, peripheral nervous system cancer, benign neoplasm of peripheral nervous system

Subtypes (12): trigeminal nerve neoplasm, abducens nerve neoplasm, facial nerve neoplasm, malignant cranial nerve neoplasm, oculomotor nerve neoplasm, hypoglossal nerve neoplasm, spinal accessory 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.