Schwannoma of twelfth cranial nerve
diseaseOn this page
Also known as hypoglossal nerve neurilemmomahypoglossal nerve schwannomahypoglossal neurilemmomahypoglossal schwannomaneurilemmoma of hypoglossal nerveneurilemmoma of the hypoglossal nerveneurilemmoma of the twelfth cranial nerveneurilemmoma of twelfth cranial nerveschwannoma of hypoglossal nerveschwannoma of the hypoglossal nerveschwannoma of the twelfth cranial nervetwelfth cranial nerve neurilemmomatwelfth cranial nerve schwannoma
Summary
Schwannoma of twelfth cranial nerve (MONDO:0002549) is a disease. A subtype of schwannoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | schwannoma of twelfth cranial nerve |
| Mondo ID | MONDO:0002549 |
| DOID | DOID:3197 |
| NCIT | C5434 |
| UMLS | C1335928 |
| MedGen | 235581 |
| GARD | 0023163 |
| Anatomy (UBERON) | UBERON:0001650 |
| Is cancer (heuristic) | no |
Also known as: hypoglossal nerve neurilemmoma · hypoglossal nerve schwannoma · hypoglossal neurilemmoma · hypoglossal schwannoma · neurilemmoma of hypoglossal nerve · neurilemmoma of the hypoglossal nerve · neurilemmoma of the twelfth cranial nerve · neurilemmoma of twelfth cranial nerve · schwannoma of hypoglossal nerve · schwannoma of the hypoglossal nerve · schwannoma of the twelfth cranial nerve · schwannoma of twelfth cranial nerve · twelfth cranial nerve neurilemmoma · twelfth cranial nerve schwannoma
Disease family
This is a subtype of schwannoma. 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 › nerve sheath neoplasm › schwannoma › schwannoma of twelfth cranial nerve
Related subtypes (9): acoustic neuroma, cellular schwannoma, sympathetic neurilemmoma, trigeminal schwannoma, microcystic/reticular schwannoma, melanotic neurilemmoma, plexiform schwannoma, peripheral nerve schwannoma, schwannomatosis
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.