Central nervous system angiosarcoma
diseaseOn this page
Also known as angiosarcoma (disease) of central nervous systemangiosarcoma of central nervous systemangiosarcoma of CNSangiosarcoma of the central nervous systemangiosarcoma of the CNScentral nervous system angiosarcoma (disease)central nervous system hemangiosarcomaCNS angiosarcomaCNS hemangiosarcomahemangiosarcoma of central nervous systemhemangiosarcoma of CNShemangiosarcoma of the central nervous systemhemangiosarcoma of the CNS
Summary
Central nervous system angiosarcoma (MONDO:0003021) is a disease. A subtype of central nervous system sarcoma — 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 | central nervous system angiosarcoma |
| Mondo ID | MONDO:0003021 |
| DOID | DOID:4504 |
| NCIT | C5450 |
| UMLS | C1332875 |
| MedGen | 272441 |
| GARD | 0023329 |
| Anatomy (UBERON) | UBERON:0001017 |
| Is cancer (heuristic) | no |
Also known as: angiosarcoma (disease) of central nervous system · angiosarcoma of central nervous system · angiosarcoma of CNS · angiosarcoma of the central nervous system · angiosarcoma of the CNS · central nervous system angiosarcoma · central nervous system angiosarcoma (disease) · central nervous system hemangiosarcoma · CNS angiosarcoma · CNS hemangiosarcoma · hemangiosarcoma of central nervous system · hemangiosarcoma of CNS · hemangiosarcoma of the central nervous system · hemangiosarcoma of the CNS
Disease family
This is a subtype of central nervous system sarcoma. 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › nervous system cancer › central nervous system cancer › central nervous system sarcoma › central nervous system angiosarcoma
Related subtypes (11): spinal cord sarcoma, brain sarcoma, central nervous system rhabdomyosarcoma, central nervous system leiomyosarcoma, central nervous system fibrosarcoma, meningeal sarcoma, intracranial extraskeletal myxoid chondrosarcoma, central nervous system extraskeletal osteosarcoma, malignant peripheral nerve sheath tumor, atypical teratoid rhabdoid tumor, isolated melanotic schwannoma
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.