Catalog

Spinocerebellar ataxia type 25

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 25 – http://id.who.int/icd/entity/8347192

Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by cerebellar ataxia and prominent sensory neuropathy.

Parents

Autosomal dominant cerebellar ataxia type 3