Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Autosomal dominant cerebellar ataxia type I
Spinocerebellar ataxia type 37
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.
This condition has no sub-types.