Spinocerebellar ataxia type 25

MONDO:0012103

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

Also known as: SCA25, spinocerebellar ataxia 25

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 25 itself.

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Where it sits in the disease tree

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Part of

↑ Autosomal dominant cerebellar ataxia type I (16)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 25 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.