Olfactory nerve neoplasm
diseaseOn this page
Also known as cranial nerve I neoplasmsfirst cranial nerve neoplasmfirst cranial nerve neoplasmsfirst cranial nerve tumorfirst cranial nerve tumourneoplasm of first cranial nerveneoplasm of olfactory nerveneoplasm of the first cranial nerveneoplasm of the olfactory nerveneoplasms, cranial nerve Ineoplasms, olfactory nerveolfactory nerve neoplasm (disease)olfactory nerve neoplasmsolfactory nerve tumorolfactory nerve tumourolfactory neural neoplasmolfactory neural tumourtumor of first cranial nervetumor of olfactory nerve
Summary
Olfactory nerve neoplasm (MONDO:0002722) 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 | olfactory nerve neoplasm |
| Mondo ID | MONDO:0002722 |
| DOID | DOID:366, DOID:8256 |
| NCIT | C5121 |
| SNOMED CT | 126967000 |
| UMLS | C0346319 |
| MedGen | 87551 |
| Anatomy (UBERON) | UBERON:0001579 |
| Is cancer (heuristic) | yes |
Also known as: cranial nerve I neoplasms · first cranial nerve neoplasm · first cranial nerve neoplasms · first cranial nerve tumor · first cranial nerve tumour · neoplasm of first cranial nerve · neoplasm of olfactory nerve · neoplasm of the first cranial nerve · neoplasm of the olfactory nerve · neoplasms, cranial nerve I · neoplasms, olfactory nerve · olfactory nerve neoplasm · olfactory nerve neoplasm (disease) · olfactory nerve neoplasms · olfactory nerve tumor · olfactory nerve tumour · olfactory neural neoplasm · olfactory neural tumour · tumor of first cranial nerve · tumor of olfactory nerve (+6 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 › olfactory 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, trochlear nerve neoplasm, vestibulocochlear nerve neoplasm
Subtypes (1): olfactory neuroblastoma
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.