Additional Disease Briefs

spinocerebellar ataxia type 19/22

Also known as: SCA19, SCA19/22, spinocerebellar ataxia 19, spinocerebellar ataxia 19 and 22, spinocerebellar ataxia 22, spinocerebellar ataxia type 19

spinocerebellar ataxia type 2

Also known as: ALS13, ATXN2 autosomal dominant cerebellar ataxia type I, OPCA2, SCA 2, SCA2, Wadia swami syndrome, Wadia-swami syndrome, amyotrophic lateral sclerosis 13, amyotrophic lateral sclerosis type 13, amyotrophic lateral sclerosis, susceptibility to, 13, autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2, cerebellar Degeneration with slow eye movements, olivopontocerebellar atrophy 2, olivopontocerebellar atrophy Holguin type, olivopontocerebellar atrophy, Holguin type, spinocerebellar Degeneration with slow eye movements, spinocerebellar ataxia 2, spinocerebellar ataxia Cuban type, spinocerebellar ataxia type 2, spinocerebellar ataxia with slow eye movements, spinocerebellar ataxia, Cuban type, spinocerebellar atrophy 2

spinocerebellar ataxia type 20

Also known as: SCA20, chromosome 11q12 duplication syndrome, 260-Kb, spinocerebellar ataxia 20, spinocerebellar ataxia type 20, spinocerebellar ataxia with dysphonia, spinocerebellar ataxia with spasmodic cough

spinocerebellar ataxia type 21

Also known as: SCA21, spinocerebellar ataxia 21, spinocerebellar ataxia type 21

spinocerebellar ataxia type 23

Also known as: SCA23, spinocerebellar ataxia 23, spinocerebellar ataxia type 23

spinocerebellar ataxia type 25

Also known as: SCA25, spinocerebellar ataxia 25

spinocerebellar ataxia type 26

Also known as: SCA26, spinocerebellar ataxia 26, spinocerebellar ataxia type 26

spinocerebellar ataxia type 27

Also known as: SCA27, cerebellar ataxia autosomal dominant FGF14-related, cerebellar ataxia, autosomal dominant, Fgf14-related, spinocerebellar ataxia 27, spinocerebellar ataxia type 27

spinocerebellar ataxia type 28

Also known as: SCA28, spinocerebellar ataxia 28, spinocerebellar ataxia type 28

spinocerebellar ataxia type 29