Disease with characteristics of early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.Three families have been reported to date. Clinical manifestations include cerebellar signs (ataxia, dysarthria, and i
ataxie spinocérébelleuse type 5
SNOMEDCT-BE (ataxia, dysarthria, and i / 719302009
SNOMEDCT-BE (disorder) / 719302009