Benign neoplasm of cerebellum
diseaseOn this page
Also known as benign cerebellar neoplasmbenign cerebellar neoplasmsbenign cerebellar tumorbenign cerebellar tumourbenign neoplasm of the cerebellumbenign tumor of cerebellumbenign tumor of the cerebellumbenign tumour of cerebellumbenign tumour of the cerebellumcerebellar neoplasms, benigncerebellum benign neoplasmneoplasms, benign, cerebellarneoplasms, cerebellar, benign
Summary
Benign neoplasm of cerebellum (MONDO:0021499) 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 | benign neoplasm of cerebellum |
| Mondo ID | MONDO:0021499 |
| ICD-11 | 664460646 |
| NCIT | C4955 |
| SNOMED CT | 92050000 |
| UMLS | C0750995 |
| MedGen | 196704 |
| Anatomy (UBERON) | UBERON:0002037 |
| Is cancer (heuristic) | yes |
Also known as: benign cerebellar neoplasm · benign cerebellar neoplasms · benign cerebellar tumor · benign cerebellar tumour · benign neoplasm of the cerebellum · benign tumor of cerebellum · benign tumor of the cerebellum · benign tumour of cerebellum · benign tumour of the cerebellum · cerebellar neoplasms, benign · cerebellum benign neoplasm · neoplasms, benign, cerebellar · neoplasms, cerebellar, benign
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 › benign neoplasm of cerebellum
Related subtypes (7): cerebellar astrocytoma, adult cerebellar neoplasm, papillary meningioma of the cerebellum, childhood cerebellar neoplasm, cerebellar liponeurocytoma, medulloblastoma, cancer of cerebellum
Subtypes (2): cerebellar pilocytic astrocytoma, 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.