Cerebellopontine angle meningioma
disease diseaseOn this page
Also known as C-P angle meningiomacerebellar Pontine angle meningiomacerebellopontine angle meningioma (disease)meningioma (disease) of cerebellopontine anglemeningioma of C-P anglemeningioma of cerebellar Pontine anglemeningioma of cerebellopontine anglemeningioma of the C-P anglemeningioma of the cerebellar Pontine anglemeningioma of the cerebellopontine angle
Summary
Cerebellopontine angle meningioma (MONDO:0003860) is a disease. A subtype of cerebellopontine angle tumor — 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 | cerebellopontine angle meningioma |
| Mondo ID | MONDO:0003860 |
| DOID | DOID:6337 |
| NCIT | C5300 |
| SNOMED CT | 126948004 |
| UMLS | C1263882 |
| MedGen | 220388 |
| GARD | 0023700 |
| Anatomy (UBERON) | UBERON:0014908 |
| Is cancer (heuristic) | no |
Also known as: C-P angle meningioma · cerebellar Pontine angle meningioma · cerebellopontine angle meningioma (disease) · meningioma (disease) of cerebellopontine angle · meningioma of C-P angle · meningioma of cerebellar Pontine angle · meningioma of cerebellopontine angle · meningioma of the C-P angle · meningioma of the cerebellar Pontine angle · meningioma of the cerebellopontine angle
Disease family
Classification path: disease › human disease › disease by body system or component › nervous system disorder › central nervous system disorder › brain disorder › brain neoplasm › cerebellopontine angle tumor › cerebellopontine angle meningioma
Related subtypes (2): c-P angle neurinoma, cerebellopontine angle embryonal tumor
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.