Brain stem hemangioblastoma
diseaseOn this page
Also known as angioblastoma of brain stemangioblastoma of brainstemangioblastoma of the brain stemangioblastoma of the brainstembrain stem angioblastomabrain stem capillary hemangioblastomabrainstem angioblastomabrainstem hemangioblastomahemangioblastoma of brain stemhemangioblastoma of brainstemhemangioblastoma of the brain stemhemangioblastoma of the brainstem
Summary
Brain stem hemangioblastoma (MONDO:0003902) is a disease. A subtype of intracranial 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 | brain stem hemangioblastoma |
| Mondo ID | MONDO:0003902 |
| DOID | DOID:6501 |
| NCIT | C5147 |
| UMLS | C1332611 |
| MedGen | 231461 |
| GARD | 0023723 |
| Anatomy (UBERON) | UBERON:0002298 |
| Is cancer (heuristic) | no |
Also known as: angioblastoma of brain stem · angioblastoma of brainstem · angioblastoma of the brain stem · angioblastoma of the brainstem · brain stem angioblastoma · brain stem capillary hemangioblastoma · brain stem hemangioblastoma · brainstem angioblastoma · brainstem hemangioblastoma · hemangioblastoma of brain stem · hemangioblastoma of brainstem · hemangioblastoma of the brain stem · hemangioblastoma of the brainstem
Disease family
This is a subtype of intracranial 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: human disease › 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 stem hemangioblastoma
Related subtypes (3): intracranial cavernous angioma, brain hemangioma, cerebellar hemangioblastoma
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.