Cerebellar vermis medulloblastoma

Summary

Cerebellar vermis medulloblastoma (MONDO:0002792) is a disease. A subtype of medulloblastoma — 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	cerebellar vermis medulloblastoma
Mondo ID	MONDO:0002792
DOID	DOID:3860
NCIT	C5401
UMLS	C1332903
MedGen	232044
GARD	0023248
Anatomy (UBERON)	UBERON:0004720
Is cancer (heuristic)	no

Also known as: cerebellar vermis medulloblastoma · medulloblastoma of cerebellar vermis · medulloblastoma of the cerebellar vermis · vermis medulloblastoma

Disease family

This is a subtype of medulloblastoma. 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 › medulloblastoma › cerebellar vermis medulloblastoma

Related subtypes (13): brain stem medulloblastoma, large cell medulloblastoma, adult medulloblastoma, melanotic medulloblastoma, childhood medulloblastoma, medullomyoblastoma with myogenic differentiation, anaplastic/large cell medulloblastoma, medulloblastoma with extensive nodularity, desmoplastic/nodular medulloblastoma, classic medulloblastoma, medulloblastoma WNT activated, medulloblastoma SHH activated, medulloblastoma non-WNT/non-SHH

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.