Trochlear nerve neoplasm
diseaseOn this page
Also known as fourth cranial nerve neoplasmfourth cranial nerve neoplasmsfourth cranial nerve tumorfourth cranial nerve tumorsfourth cranial nerve tumourfourth cranial nerve tumoursIVth cranial nerve neoplasmsIVth cranial nerve tumorsIVth cranial nerve tumoursneoplasm of fourth cranial nerveneoplasm of the fourth cranial nerveneoplasm of the trochlear nerveneoplasm of trochlear nervetrochlear nerve neoplasm (disease)trochlear nerve neoplasmstrochlear nerve tumortrochlear nerve tumorstrochlear nerve tumourtrochlear nerve tumourstumor of fourth cranial nerve
Summary
Trochlear nerve neoplasm (MONDO:0002642) 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 | trochlear nerve neoplasm |
| Mondo ID | MONDO:0002642 |
| DOID | DOID:3421 |
| NCIT | C5825 |
| SNOMED CT | 126970001 |
| UMLS | C1263896 |
| MedGen | 226811 |
| Anatomy (UBERON) | UBERON:0001644 |
| Is cancer (heuristic) | yes |
Also known as: fourth cranial nerve neoplasm · fourth cranial nerve neoplasms · fourth cranial nerve tumor · fourth cranial nerve tumors · fourth cranial nerve tumour · fourth cranial nerve tumours · IVth cranial nerve neoplasms · IVth cranial nerve tumors · IVth cranial nerve tumours · neoplasm of fourth cranial nerve · neoplasm of the fourth cranial nerve · neoplasm of the trochlear nerve · neoplasm of trochlear nerve · trochlear nerve neoplasm (disease) · trochlear nerve neoplasms · trochlear nerve tumor · trochlear nerve tumors · trochlear nerve tumour · trochlear nerve tumours · tumor of fourth 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 disorder › peripheral nervous system disorder › peripheral nervous system neoplasm › cranial nerve neoplasm › trochlear nerve neoplasm
Related subtypes (11): 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, 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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.