FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	cerebellar disease	ID (Ontology)	DOID:2786 (Human Disease)
Definition	A brain disease that is characterized by damage to brain substance located_in cerebellum; has_symptom ataxia, has_symptom dysarthria, and has_symptom cerebellar cognitive affective syndrome.
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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Spanning Tree (Parents/Children)

  central nervous system disease
   |__brain disease
       |__cerebellar disease  1095 rec.
           |__cerebellar ataxia 1092 rec.
           |   |__autosomal dominant cerebellar ataxia(+) 895 rec.
           |   |__autosomal recessive cerebellar ataxia(+) 209 rec.
           |__cerebellar hypoplasia 2 rec.
           |__cerebellum cancer
           |   |__adult cerebellar neoplasm
           |   |__cerebellar angioblastoma
           |   |__cerebellar astrocytoma(+)
           |   |__cerebellar liponeurocytoma
           |   |__cerebellar medulloblastoma(+)
           |   |__childhood cerebellar neoplasm
           |   |__papillary meningioma of the cerebellum
           |__Dandy-Walker syndrome
           |__L-2-hydroxyglutaric aciduria 1 rec.

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Relationships
Is a	brain disease
Part of
Synonyms & Secondary IDs
Synonyms

Secondary IDs

External Crossreferences & Linkouts
	MESH:D002526 SNOMEDCT_US_2023_03_01:267691001 UMLS_CUI:C0007760