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Human Disease

spinocerebellar ataxia type 20

Term ID
DOID:0050971
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by cerebellar dysarthria. https://rarediseases.info.nih.gov/diseases/9997/spinocerebellar-ataxia-20
References
Ontology
Human Disease   ( DOID:0050971 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations