Adult cerebellar neoplasm
diseaseOn this page
Also known as adult cerebellar neoplasmsadult cerebellar tumoradult cerebellar tumorsadult cerebellar tumouradult cerebellar tumourscerebellar neoplasm of adultsneoplasm of adult cerebellumneoplasm of the adult cerebellumtumor of adult cerebellumtumor of the adult cerebellumtumour of adult cerebellumtumour of the adult cerebellum
Summary
Adult cerebellar neoplasm (MONDO:0003260) is a cancer. A subtype of cerebellar neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | adult cerebellar neoplasm |
| Mondo ID | MONDO:0003260 |
| DOID | DOID:5056 |
| NCIT | C5968 |
| UMLS | C1332197 |
| MedGen | 272293 |
| Is cancer (heuristic) | yes |
Also known as: adult cerebellar neoplasm · adult cerebellar neoplasms · adult cerebellar tumor · adult cerebellar tumors · adult cerebellar tumour · adult cerebellar tumours · cerebellar neoplasm of adults · neoplasm of adult cerebellum · neoplasm of the adult cerebellum · tumor of adult cerebellum · tumor of the adult cerebellum · tumour of adult cerebellum · tumour of the adult cerebellum
Disease family
This is a subtype of cerebellar neoplasm. 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 body system or component › nervous system disorder › central nervous system disorder › brain disorder › cerebellar disorder › cerebellar neoplasm › adult cerebellar neoplasm
Related subtypes (7): cerebellar astrocytoma, papillary meningioma of the cerebellum, childhood cerebellar neoplasm, cerebellar liponeurocytoma, medulloblastoma, cancer of cerebellum, benign neoplasm of cerebellum
Subtypes (1): adult medulloblastoma
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.