Cerebellar neoplasm

disease

On this page

Also known as cerebellar tumorcerebellar tumourcerebellum neoplasmcerebellum neoplasm (disease)cerebellum tumorcerebellum tumourmalignant tumor of cerebellummalignant tumour of cerebellumneoplasm of cerebellumneoplasm of the cerebellumtumor of cerebellumtumor of the cerebellumtumour of cerebellumtumour of the cerebellum

Summary

Cerebellar neoplasm (MONDO:0002913) is a cancer (an umbrella term covering 8 Mondo subtypes) and 4 clinical trials. A subtype of cerebellar disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

Classification: Cancer
Umbrella term: 8 Mondo subtypes
Clinical trials: 4

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	cerebellar neoplasm
Mondo ID	MONDO:0002913
MeSH	D002528
DOID	DOID:4205
NCIT	C2935
SNOMED CT	126960003
UMLS	C0007762
MedGen	40187
Anatomy (UBERON)	UBERON:0002037
Is cancer (heuristic)	yes

Also known as: cerebellar neoplasm · cerebellar tumor · cerebellar tumour · cerebellum neoplasm · cerebellum neoplasm (disease) · cerebellum tumor · cerebellum tumour · malignant tumor of cerebellum · malignant tumour of cerebellum · neoplasm of cerebellum · neoplasm of the cerebellum · tumor of cerebellum · tumor of the cerebellum · tumour of cerebellum · tumour of the cerebellum

Disease family

This is a subtype of cerebellar disorder. 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

Subtypes (8): cerebellar astrocytoma, adult cerebellar neoplasm, papillary meningioma of the cerebellum, childhood cerebellar neoplasm, cerebellar liponeurocytoma, medulloblastoma, cancer of cerebellum, benign neoplasm of cerebellum

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: 4.

Phase distribution (across all retrieved trials)

Phase	Trials
Not specified	3
PHASE1	1

Top trials by phase / activity

NCT	Phase	Status	Title
NCT03911388	PHASE1	RECRUITING	HSV G207 in Children With Recurrent or Refractory Cerebellar Brain Tumors
NCT04463979	Not specified	ACTIVE_NOT_RECRUITING	Perioperative Evaluation of Cerebellar Tumors
NCT02261649	Not specified	COMPLETED	Impact of Cerebellar Mass Resection on Pain Processing
NCT05998486	Not specified	UNKNOWN	Detecting the Rest Tremor Associated With Parkinson’s Disease Using Analysis of the Muscle Contractions Rhythmicity

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.