Childhood cerebellar neoplasm
diseaseOn this page
Also known as childhood cerebellar neoplasmschildhood cerebellar tumorchildhood cerebellar tumorschildhood cerebellar tumourchildhood cerebellar tumourschildhood neoplasm of cerebellumchildhood neoplasm of the cerebellumchildhood tumor of cerebellumchildhood tumor of the cerebellumchildhood tumour of cerebellumchildhood tumour of the cerebellumpaediatric cerebellar neoplasmpaediatric cerebellar tumourpaediatric neoplasm of cerebellumpaediatric neoplasm of the cerebellumpaediatric tumour of cerebellumpaediatric tumour of the cerebellumpediatric cerebellar neoplasmpediatric cerebellar tumor
Summary
Childhood cerebellar neoplasm (MONDO:0003263) is a cancer and 1 clinical trial. 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 trials: 1
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | childhood cerebellar neoplasm |
| Mondo ID | MONDO:0003263 |
| DOID | DOID:5059 |
| NCIT | C5970 |
| UMLS | C1332959 |
| MedGen | 234124 |
| Is cancer (heuristic) | yes |
Also known as: childhood cerebellar neoplasm · childhood cerebellar neoplasms · childhood cerebellar tumor · childhood cerebellar tumors · childhood cerebellar tumour · childhood cerebellar tumours · childhood neoplasm of cerebellum · childhood neoplasm of the cerebellum · childhood tumor of cerebellum · childhood tumor of the cerebellum · childhood tumour of cerebellum · childhood tumour of the cerebellum · paediatric cerebellar neoplasm · paediatric cerebellar tumour · paediatric neoplasm of cerebellum · paediatric neoplasm of the cerebellum · paediatric tumour of cerebellum · paediatric tumour of the cerebellum · pediatric cerebellar neoplasm · pediatric cerebellar tumor (+4 more)
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 › childhood cerebellar neoplasm
Related subtypes (7): cerebellar astrocytoma, adult cerebellar neoplasm, papillary meningioma of the cerebellum, cerebellar liponeurocytoma, medulloblastoma, cancer of cerebellum, benign neoplasm of cerebellum
Subtypes (2): childhood medulloblastoma, childhood cerebellar astrocytic neoplasm
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: 1.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01730274 | Not specified | COMPLETED | Cerebellum - Cognitive Outcome and Functional Connectivity |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.