Trigeminal nerve neoplasm

disease
On this page

Also known as cranial nerve V neoplasmscranial nerve V tumorscranial nerve V tumoursfifth cranial nerve neoplasmfifth cranial nerve tumorfifth cranial nerve tumourneoplasm of fifth cranial nerveneoplasm of the fifth cranial nerveneoplasm of the trigeminal nerveneoplasm of trigeminal nerveneoplasms, cranial nerve Vtrigeminal nerve neoplasm (disease)trigeminal nerve neoplasmstrigeminal nerve tumortrigeminal nerve tumorstrigeminal nerve tumourtrigeminal nerve tumourstumor of fifth cranial nervetumor of the fifth cranial nerve

Summary

Trigeminal nerve neoplasm (MONDO:0001420) 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

FieldValue
Canonical nametrigeminal nerve neoplasm
Mondo IDMONDO:0001420
DOIDDOID:1201
NCITC5122
SNOMED CT126971002
UMLSC1263897
MedGen226812
Anatomy (UBERON)UBERON:0001645
Is cancer (heuristic)yes

Also known as: cranial nerve V neoplasms · cranial nerve V tumors · cranial nerve V tumours · fifth cranial nerve neoplasm · fifth cranial nerve tumor · fifth cranial nerve tumour · neoplasm of fifth cranial nerve · neoplasm of the fifth cranial nerve · neoplasm of the trigeminal nerve · neoplasm of trigeminal nerve · neoplasms, cranial nerve V · trigeminal nerve neoplasm · trigeminal nerve neoplasm (disease) · trigeminal nerve neoplasms · trigeminal nerve tumor · trigeminal nerve tumors · trigeminal nerve tumour · trigeminal nerve tumours · tumor of fifth cranial nerve · tumor of the fifth cranial nerve (+7 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 disorderperipheral nervous system disorderperipheral nervous system neoplasmcranial nerve neoplasmtrigeminal nerve neoplasm

Related subtypes (11): 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

Subtypes (1): trigeminal schwannoma

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.