Spinocerebellar ataxia type 37

MONDO:0014410

Spinocerebellar ataxia type 37 (SCA37) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1), characterized by a cerebellar syndrome along with altered vertical eye movements.

Also known as: SCA37, spinocerebellar ataxia with altered vertical eye movements, spinocerebellar ataxia 37

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 37 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 37 (0)

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