Abducens nerve neoplasm
diseaseOn this page
Also known as abducens nerve neoplasm (disease)abducens nerve neoplasmsabducens nerve tumorabducens nerve tumorsabducens nerve tumourabducens nerve tumoursneoplasm of abducens nerveneoplasm of sixth cranial nerveneoplasm of the abducens nerveneoplasm of the sixth cranial nervesixth cranial nerve neoplasmsixth cranial nerve neoplasmssixth cranial nerve tumorsixth cranial nerve tumorssixth cranial nerve tumoursixth cranial nerve tumourstumor of abducens nervetumor of sixth cranial nervetumor of the abducens nervetumor of the sixth cranial nerve
Summary
Abducens nerve neoplasm (MONDO:0001884) 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 | abducens nerve neoplasm |
| Mondo ID | MONDO:0001884 |
| DOID | DOID:14125 |
| NCIT | C5826 |
| SNOMED CT | 126972009 |
| UMLS | C1263898 |
| MedGen | 224732 |
| Anatomy (UBERON) | UBERON:0001646 |
| Is cancer (heuristic) | yes |
Also known as: abducens nerve neoplasm (disease) · abducens nerve neoplasms · abducens nerve tumor · abducens nerve tumors · abducens nerve tumour · abducens nerve tumours · neoplasm of abducens nerve · neoplasm of sixth cranial nerve · neoplasm of the abducens nerve · neoplasm of the sixth cranial nerve · sixth cranial nerve neoplasm · sixth cranial nerve neoplasms · sixth cranial nerve tumor · sixth cranial nerve tumors · sixth cranial nerve tumour · sixth cranial nerve tumours · tumor of abducens nerve · tumor of sixth cranial nerve · tumor of the abducens nerve · tumor of the sixth 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 › abducens nerve neoplasm
Related subtypes (11): trigeminal 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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.