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Spinocerebellar Ataxias MeSH Descriptor Data 2021


MeSH Heading
Spinocerebellar Ataxias
Tree 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
Unique ID
D020754
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D020754
Annotation
SPINOCEREBELLAR ATAXIA TYPE 3 see MACHADO-JOSEPH DISEASE is available
Scope Note
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)
Entry Term(s)
Autosomal Dominant Cerebellar Ataxia, Type II
Cerebellar Degeneration with Slow Eye Movements
Cerebelloparenchymal Disorder I
Dominantly-Inherited Spinocerebellar Ataxias
Menzel Type OPCA
OPCA with Macular Degeneration and External Ophthalmoplegia
OPCA with Retinal Degeneration
Olivopontocerebellar Atrophy 2
Olivopontocerebellar Atrophy I
Olivopontocerebellar Atrophy II
Olivopontocerebellar Atrophy III
Olivopontocerebellar Atrophy IV
Olivopontocerebellar Atrophy, Holguin Type
SCA1
Schut-Haymaker Type OPCA
Spinocerebellar Ataxia 1
Spinocerebellar Ataxia 2
Spinocerebellar Ataxia 4
Spinocerebellar Ataxia 5
Spinocerebellar Ataxia 6
Spinocerebellar Ataxia 7
Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 6
Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia with Slow Eye Movements
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
Spinocerebellar Ataxia, Cuban Type
Spinocerebellar Ataxia-1
Spinocerebellar Ataxia-2
Spinocerebellar Ataxia-4
Spinocerebellar Ataxia-5
Spinocerebellar Ataxia-6
Spinocerebellar Ataxia-7
Spinocerebellar Ataxias, Dominantly-Inherited
Spinocerebellar Atrophies
Spinocerebellar Atrophy 2
Spinocerebellar Atrophy I
Spinocerebellar Atrophy II
Spinocerebellar Degeneration with Slow Eye Movements
Type 1 Spinocerebellar Ataxia
Type 2 Spinocerebellar Ataxia
Type 4 Spinocerebellar Ataxia
Type 5 Spinocerebellar Ataxia
Type 6 Spinocerebellar Ataxia
Type 7 Spinocerebellar Ataxia
Wadia Swami Syndrome
Wadia-Swami Syndrome
Previous Indexing
Ataxia/genetics (1965-1999)
Cerebellar Diseases (1966-1999)
Spinal Cord Diseases (1966-1999)
Spinocerebellar Degenerations (1987-1999)
See Also
Ataxin-1
Ataxin-2
Ataxin-3
Ataxin-7
Ataxins
Public MeSH Note
2000; see SPINOCEREBELLAR DEGENERATION 1987-1999
History Note
2000; use SPINOCEREBELLAR DEGENERATION 1987-1999
Date Established
2000/01/01
Date of Entry
1999/11/08
Revision Date
2015/02/19
Spinocerebellar Ataxias Preferred
Spinocerebellar Ataxia Type 2 Narrower
Spinocerebellar Ataxia Type 7 Narrower
Spinocerebellar Ataxia Type 5 Narrower
Spinocerebellar Ataxia Type 6 Narrower
Spinocerebellar Ataxia Type 1 Narrower
Spinocerebellar Ataxia Type 4 Narrower
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