Search Ontology:
Human Disease

spinocerebellar ataxia 19/22

Term ID
DOID:0050970
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor. https://rarediseases.info.nih.gov/diseases/12365/spinocerebellar-ataxia-19-and-22
References
Ontology
Human Disease   ( DOID:0050970 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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