Disease with characteristics of early-onset cerebellar signs, eye movement abnormalities and pyramidal signs. Fifty-one clinically affected members from four families (of British, Pakistani, German and French descent) have been reported to date. The
ataxie spinocérébelleuse type 11
SNOMEDCT-BE (of British, Pakistani, German and French descent) have been reported to date. The / 719207000
SNOMEDCT-BE (disorder) / 719207000