Catalog

Spinocerebellar ataxia type 11

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 11 – http://id.who.int/icd/entity/743674840

Spinocerebellar ataxia type 11 is a subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs and caused by a mutation in the TTBK2 gene.