A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)

Descriptor ID	D020754
MeSH Number(s)	C10.228.140.252.190.530 C10.228.140.252.700.700 C10.228.854.787.875 C10.574.500.825.700 C10.597.350.090.500.530 C16.320.400.780.875
Concept/Terms	Spinocerebellar Ataxias Spinocerebellar Ataxias Ataxia, Spinocerebellar Ataxias, Spinocerebellar Spinocerebellar Ataxia Spinocerebellar Atrophies Atrophies, Spinocerebellar Atrophy, Spinocerebellar Spinocerebellar Atrophy Dominantly-Inherited Spinocerebellar Ataxias Ataxia, Dominantly-Inherited Spinocerebellar Ataxias, Dominantly-Inherited Spinocerebellar Dominantly Inherited Spinocerebellar Ataxias Dominantly-Inherited Spinocerebellar Ataxia Spinocerebellar Ataxia, Dominantly-Inherited Spinocerebellar Ataxias, Dominantly-Inherited Spinocerebellar Ataxias, Dominantly Inherited Spinocerebellar Ataxia Type 5 Spinocerebellar Ataxia Type 5 Spinocerebellar Ataxia-5 Type 5 Spinocerebellar Ataxia Spinocerebellar Ataxia 5 5, Spinocerebellar Ataxia Ataxia 5, Spinocerebellar Ataxia 5s, Spinocerebellar Spinocerebellar Ataxia 5s Spinocerebellar Ataxia Type 6 Spinocerebellar Ataxia Type 6 Spinocerebellar Ataxia-6 Type 6 Spinocerebellar Ataxia Spinocerebellar Ataxia 6 Ataxia 6, Spinocerebellar Ataxia 6s, Spinocerebellar Spinocerebellar Ataxia 6s Spinocerebellar Ataxia Type 2 Spinocerebellar Ataxia Type 2 Wadia-Swami Syndrome Syndrome, Wadia-Swami Spinocerebellar Ataxia-2 Type 2 Spinocerebellar Ataxia Cerebellar Degeneration with Slow Eye Movements Spinocerebellar Ataxia 2 Ataxia 2, Spinocerebellar Ataxia 2s, Spinocerebellar Spinocerebellar Ataxia 2s Spinocerebellar Ataxia Type 4 Spinocerebellar Ataxia Type 4 Type 4 Spinocerebellar Ataxia Spinocerebellar Ataxia-4 Spinocerebellar Ataxia 4 Ataxia 4, Spinocerebellar Ataxia 4s, Spinocerebellar Spinocerebellar Ataxia 4s Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy Spinocerebellar Ataxia Type 7 Spinocerebellar Ataxia Type 7 OPCA with Macular Degeneration and External Ophthalmoplegia OPCA with Retinal Degeneration Olivopontocerebellar Atrophy III Atrophy III, Olivopontocerebellar Olivopontocerebellar Atrophy IIIs Type 7 Spinocerebellar Ataxia Autosomal Dominant Cerebellar Ataxia, Type II Spinocerebellar Ataxia-7 Spinocerebellar Ataxia 7 Ataxia 7, Spinocerebellar Ataxia 7s, Spinocerebellar Spinocerebellar Ataxia 7s Spinocerebellar Ataxia Type 1 Spinocerebellar Ataxia Type 1 Menzel Type OPCA OPCA, Menzel Type Olivopontocerebellar Atrophy I Atrophy I, Olivopontocerebellar Olivopontocerebellar Atrophy Is Olivopontocerebellar Atrophy IV Spinocerebellar Ataxia 1 Ataxia 1, Spinocerebellar Spinocerebellar Ataxia 1s Spinocerebellar Ataxia-1 Spinocerebellar Atrophy I Atrophy I, Spinocerebellar Spinocerebellar Atrophy Is Type 1 Spinocerebellar Ataxia Cerebelloparenchymal Disorder I Cerebelloparenchymal Disorder Is Schut-Haymaker Type OPCA OPCA, Schut-Haymaker Type Schut Haymaker Type OPCA

Below are MeSH descriptors whose meaning is more general than "Spinocerebellar Ataxias".

Below are MeSH descriptors whose meaning is related to "Spinocerebellar Ataxias".

Below are MeSH descriptors whose meaning is more specific than "Spinocerebellar Ataxias".