Cerebral meningioma
disease diseaseOn this page
Also known as cerebral hemispheric meningiomameningioma (disease) of telencephalonmeningioma of cerebral hemispheresmeningioma of cerebrummeningioma of the cerebral hemispheresmeningioma of the cerebrumtelencephalon meningioma (disease)
Summary
Cerebral meningioma (MONDO:0003772) is a disease. A subtype of cerebral hemisphere cancer — 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 | cerebral meningioma |
| Mondo ID | MONDO:0003772 |
| DOID | DOID:6112 |
| NCIT | C4807 |
| SNOMED CT | 189164002 |
| UMLS | C0542564 |
| MedGen | 154239 |
| GARD | 0023663 |
| Anatomy (UBERON) | UBERON:0001893 |
| Is cancer (heuristic) | no |
Also known as: cerebral hemispheric meningioma · meningioma (disease) of telencephalon · meningioma of cerebral hemispheres · meningioma of cerebrum · meningioma of the cerebral hemispheres · meningioma of the cerebrum · telencephalon meningioma (disease)
Disease family
An umbrella term covering 4 Mondo subtypes.
Classification path: disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › nervous system cancer › central nervous system cancer › brain cancer › supratentorial cancer › cerebral hemisphere cancer › cerebral meningioma
Related subtypes (9): corpus callosum oligodendroglioma, parietal lobe cancer, temporal lobe cancer, cerebral neuroblastoma, cerebral lymphoma, childhood cerebral astrocytoma, cerebral primitive neuroectodermal tumor, pediatric cerebral ependymoblastoma, frontal lobe ependymal tumor
Subtypes (4): intracerebral cystic meningioma, cerebral convexity meningioma, lateral ventricle meningioma, parasagittal meningioma
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.