Human genes for spinocerebellar ataxia type 19/22
Spinocerebellar ataxia type 19/22 [DOID:0050970]
An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor.
Synonyms: spinocerebellar ataxia type 19/22, DOID:0050970