Cerebral hemangioma
disease diseaseOn this page
Also known as angioma of cerebral hemispheresangioma of cerebrumangioma of the cerebral hemispheresangioma of the cerebrumcerebral angiomacerebral hemispheric angiomacerebral hemispheric hemangiomahemangioma of cerebral hemisphereshemangioma of cerebrumhemangioma of telencephalonhemangioma of the cerebral hemisphereshemangioma of the cerebrumtelencephalon hemangioma
Summary
Cerebral hemangioma (MONDO:0003948) is a disease. A subtype of brain hemangioma — 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 hemangioma |
| Mondo ID | MONDO:0003948 |
| DOID | DOID:6621 |
| NCIT | C5433 |
| UMLS | C0877388 |
| MedGen | 164084 |
| Anatomy (UBERON) | UBERON:0001893 |
| Is cancer (heuristic) | no |
Also known as: angioma of cerebral hemispheres · angioma of cerebrum · angioma of the cerebral hemispheres · angioma of the cerebrum · cerebral angioma · cerebral hemangioma · cerebral hemispheric angioma · cerebral hemispheric hemangioma · hemangioma of cerebral hemispheres · hemangioma of cerebrum · hemangioma of telencephalon · hemangioma of the cerebral hemispheres · hemangioma of the cerebrum · telencephalon hemangioma
Disease family
This is a subtype of brain hemangioma. 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 by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › benign neoplasm › nervous system benign neoplasm › central nervous system organ benign neoplasm › central nervous system hemangioma › intracranial hemangioma › brain hemangioma › cerebral hemangioma
Subtypes (1): vein of Galen aneurysm
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.