Spinocerebellar Ataxias

"Spinocerebellar Ataxias" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 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 Atrophies Atrophies, Spinocerebellar Atrophy, Spinocerebellar Spinocerebellar Atrophy Spinocerebellar Ataxia Type 2 Spinocerebellar Ataxia Type 2 Type 2 Spinocerebellar Ataxia Spinocerebellar Ataxia 2 Ataxia 2, Spinocerebellar Ataxia 2s, Spinocerebellar Spinocerebellar Ataxia 2s Wadia-Swami Syndrome Syndrome, Wadia-Swami Cerebellar Degeneration with Slow Eye Movements Olivopontocerebellar Atrophy II Atrophy II, Olivopontocerebellar Atrophy IIs, Olivopontocerebellar II, Olivopontocerebellar Atrophy IIs, Olivopontocerebellar Atrophy Olivopontocerebellar Atrophy IIs Spinocerebellar Atrophy II Atrophy II, Spinocerebellar Atrophy IIs, Spinocerebellar II, Spinocerebellar Atrophy IIs, Spinocerebellar Atrophy Spinocerebellar Atrophy IIs Olivopontocerebellar Atrophy 2 Atrophy 2, Olivopontocerebellar Atrophy 2s, Olivopontocerebellar Olivopontocerebellar Atrophy 2s Spinocerebellar Ataxia with Slow Eye Movements Spinocerebellar Ataxia, Cuban Type Spinocerebellar Atrophy 2 Atrophy 2, Spinocerebellar Atrophy 2s, Spinocerebellar Spinocerebellar Atrophy 2s Spinocerebellar Degeneration with Slow Eye Movements Wadia Swami Syndrome Swami Syndrome, Wadia Syndrome, Wadia Swami Olivopontocerebellar Atrophy, Holguin Type Spinocerebellar Ataxia-2 Spinocerebellar Ataxia Type 7 Spinocerebellar Ataxia Type 7 Type 7 Spinocerebellar Ataxia OPCA with Retinal Degeneration Olivopontocerebellar Atrophy III Atrophy III, Olivopontocerebellar Olivopontocerebellar Atrophy IIIs Autosomal Dominant Cerebellar Ataxia, Type II OPCA with Macular Degeneration and External Ophthalmoplegia Spinocerebellar Ataxia-7 Spinocerebellar Ataxia 7 Ataxia 7, Spinocerebellar Ataxia 7s, Spinocerebellar Spinocerebellar Ataxia 7s Spinocerebellar Ataxia Type 5 Spinocerebellar Ataxia Type 5 Type 5 Spinocerebellar Ataxia Spinocerebellar Ataxia 5 Ataxia 5, Spinocerebellar Ataxia 5s, Spinocerebellar Spinocerebellar Ataxia 5s Spinocerebellar Ataxia-5 Spinocerebellar Ataxia Type 6 Spinocerebellar Ataxia Type 6 Type 6 Spinocerebellar Ataxia Spinocerebellar Ataxia 6 Ataxia 6, Spinocerebellar Ataxia 6s, Spinocerebellar Spinocerebellar Ataxia 6s Spinocerebellar Ataxia-6 Spinocerebellar Ataxia Type 1 Spinocerebellar Ataxia Type 1 Type 1 Spinocerebellar Ataxia Spinocerebellar Ataxia 1 Ataxia 1, Spinocerebellar Spinocerebellar Ataxia 1s Spinocerebellar Atrophy I Atrophy I, Spinocerebellar Spinocerebellar Atrophy Is SCA1 SCA1s Cerebelloparenchymal Disorder I Cerebelloparenchymal Disorder Is Menzel Type OPCA OPCA, Menzel Type Schut-Haymaker Type OPCA OPCA, Schut-Haymaker Type Schut Haymaker Type OPCA Olivopontocerebellar Atrophy IV Atrophy IV, Olivopontocerebellar Atrophy IVs, Olivopontocerebellar Olivopontocerebellar Atrophy IVs Spinocerebellar Ataxia-1 Olivopontocerebellar Atrophy I Atrophy I, Olivopontocerebellar Olivopontocerebellar Atrophy Is Spinocerebellar Ataxia Type 4 Spinocerebellar Ataxia Type 4 Spinocerebellar Ataxia 4 Ataxia 4, Spinocerebellar Ataxia 4s, Spinocerebellar Spinocerebellar Ataxia 4s Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy Spinocerebellar Ataxia-4 Type 4 Spinocerebellar Ataxia

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

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Cerebellar Diseases [C10.228.140.252]
Cerebellar Ataxia [C10.228.140.252.190]
Spinocerebellar Ataxias [C10.228.140.252.190.530]
Spinocerebellar Degenerations [C10.228.140.252.700]
Spinocerebellar Ataxias [C10.228.140.252.700.700]
Spinal Cord Diseases [C10.228.854]
Spinocerebellar Degenerations [C10.228.854.787]
Spinocerebellar Ataxias [C10.228.854.787.875]
Neurodegenerative Diseases [C10.574]
Heredodegenerative Disorders, Nervous System [C10.574.500]
Spinocerebellar Degenerations [C10.574.500.825]
Spinocerebellar Ataxias [C10.574.500.825.700]
Neurologic Manifestations [C10.597]
Dyskinesias [C10.597.350]
Ataxia [C10.597.350.090]
Cerebellar Ataxia [C10.597.350.090.500]
Spinocerebellar Ataxias [C10.597.350.090.500.530]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Spinocerebellar Degenerations [C16.320.400.780]
Spinocerebellar Ataxias [C16.320.400.780.875]

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

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

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This graph shows the total number of publications written about "Spinocerebellar Ataxias" by people in this website by year, and whether "Spinocerebellar Ataxias" was a major or minor topic of these publications.

Bar chart showing 2 publications over 2 distinct years, with a maximum of 1 publications in 2015 and 2020

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Year	Major Topic	Minor Topic	Total
2015	1	0	1
2020	1	0	1

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