Search Ontology:
Human Disease

spinocerebellar ataxia type 21

Term ID
DOID:0050972
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by progressive cerebellar ataxia, cognitive impairment, tremor, bradykinesia and rigidity. https://rarediseases.info.nih.gov/diseases/9999/spinocerebellar-ataxia-21
References
Ontology
Human Disease   ( DOID:0050972 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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