| Descriptor English: | Spinocerebellar Ataxias | ||||||
| Descriptor Spanish: |
Ataxias Espinocerebelosas
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| Descriptor Portuguese: | Ataxias Espinocerebelares | ||||||
| Descriptor French: | Ataxies spinocérébelleuses | ||||||
| Entry term(s): |
Ataxia 1, Spinocerebellar Ataxia 2, Spinocerebellar Ataxia 2s, Spinocerebellar Ataxia 4, Spinocerebellar Ataxia 4s, Spinocerebellar Ataxia 5, Spinocerebellar Ataxia 5s, Spinocerebellar Ataxia 6, Spinocerebellar Ataxia 6s, Spinocerebellar Ataxia 7, Spinocerebellar Ataxia 7s, Spinocerebellar Ataxia, Dominantly-Inherited Spinocerebellar Ataxia, Spinocerebellar Ataxias, Dominantly-Inherited Spinocerebellar Ataxias, Spinocerebellar Atrophies, Spinocerebellar Atrophy 2, Olivopontocerebellar Atrophy 2, Spinocerebellar Atrophy 2s, Olivopontocerebellar Atrophy 2s, Spinocerebellar Atrophy I, Olivopontocerebellar Atrophy I, Spinocerebellar Atrophy II, Olivopontocerebellar Atrophy II, Spinocerebellar Atrophy III, Olivopontocerebellar Atrophy IIs, Olivopontocerebellar Atrophy IIs, Spinocerebellar Atrophy IV, Olivopontocerebellar Atrophy IVs, Olivopontocerebellar Atrophy, Spinocerebellar Autosomal Dominant Cerebellar Ataxia, Type II Cerebellar Degeneration with Slow Eye Movements Cerebelloparenchymal Disorder I Cerebelloparenchymal Disorder Is Dominantly Inherited Spinocerebellar Ataxias Dominantly-Inherited Spinocerebellar Ataxia Dominantly-Inherited Spinocerebellar Ataxias II, Olivopontocerebellar Atrophy II, Spinocerebellar Atrophy IIs, Olivopontocerebellar Atrophy IIs, Spinocerebellar Atrophy Menzel Type OPCA OPCA with Macular Degeneration and External Ophthalmoplegia OPCA with Retinal Degeneration OPCA, Menzel Type OPCA, Schut-Haymaker Type Olivopontocerebellar Atrophy 2 Olivopontocerebellar Atrophy 2s Olivopontocerebellar Atrophy I Olivopontocerebellar Atrophy II Olivopontocerebellar Atrophy III Olivopontocerebellar Atrophy IIIs Olivopontocerebellar Atrophy IIs Olivopontocerebellar Atrophy IV Olivopontocerebellar Atrophy IVs Olivopontocerebellar Atrophy Is Olivopontocerebellar Atrophy, Holguin Type SCA1 SCA1s Schut Haymaker Type OPCA Schut-Haymaker Type OPCA Spinocerebellar Ataxia Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 1s Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 2s Spinocerebellar Ataxia 4 Spinocerebellar Ataxia 4s Spinocerebellar Ataxia 5 Spinocerebellar Ataxia 5s Spinocerebellar Ataxia 6 Spinocerebellar Ataxia 6s Spinocerebellar Ataxia 7 Spinocerebellar Ataxia 7s 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, Dominantly-Inherited Spinocerebellar Ataxia-1 Spinocerebellar Ataxia-2 Spinocerebellar Ataxia-4 Spinocerebellar Ataxia-5 Spinocerebellar Ataxia-6 Spinocerebellar Ataxia-7 Spinocerebellar Ataxias, Dominantly Inherited Spinocerebellar Ataxias, Dominantly-Inherited Spinocerebellar Ataxias, Dominantly-Inherited Spinocerebellar Atrophies Spinocerebellar Atrophy Spinocerebellar Atrophy 2 Spinocerebellar Atrophy 2s Spinocerebellar Atrophy I Spinocerebellar Atrophy II Spinocerebellar Atrophy IIs Spinocerebellar Atrophy Is Spinocerebellar Degeneration with Slow Eye Movements Swami Syndrome, Wadia Syndrome, Wadia Swami Syndrome, Wadia-Swami 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 |
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| 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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020754 | ||||||
| Scope note: | A group of 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) |
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| Annotation: | SPINOCEREBELLAR ATAXIA TYPE 3 see MACHADO-JOSEPH DISEASE is available |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Ataxia/genetics (1965-1999) Cerebellar Diseases (1966-1999) Spinal Cord Diseases (1966-1999) Spinocerebellar Degenerations (1987-1999) |
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| Public MeSH Note: | 2000; see SPINOCEREBELLAR DEGENERATION 1987-1999 |
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| History Note: | 2000; use SPINOCEREBELLAR DEGENERATION 1987-1999 |
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| Related: |
Ataxin-1
MeSH Ataxin-2 MeSH Ataxin-3 MeSH Ataxin-7 MeSH Ataxins MeSH | ||||||
| DeCS ID: | 34243 | ||||||
| Unique ID: | D020754 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2000/01/01 | ||||||
| Date of Entry: | 1999/11/08 | ||||||
| Revision Date: | 2015/02/19 |
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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
Dominantly-Inherited Spinocerebellar Ataxias
- Preferred
| Concept UI |
M0020337 |
| Scope note | A group of 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) |
| Preferred term | Spinocerebellar Ataxias |
| Entry term(s) |
Ataxia, Spinocerebellar Ataxias, Spinocerebellar Atrophies, Spinocerebellar Atrophy, Spinocerebellar Spinocerebellar Ataxia Spinocerebellar Atrophies Spinocerebellar Atrophy |
| Concept UI |
M0336156 |
| Scope note | A group of 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) |
| Scope note | A group of 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) |
| Preferred term | Spinocerebellar Ataxia Type 2 |
| Entry term(s) |
Ataxia 2, Spinocerebellar Ataxia 2s, Spinocerebellar Atrophy 2, Olivopontocerebellar Atrophy 2, Spinocerebellar Atrophy 2s, Olivopontocerebellar Atrophy 2s, Spinocerebellar Atrophy II, Olivopontocerebellar Atrophy II, Spinocerebellar Atrophy IIs, Olivopontocerebellar Atrophy IIs, Spinocerebellar Cerebellar Degeneration with Slow Eye Movements II, Olivopontocerebellar Atrophy II, Spinocerebellar Atrophy IIs, Olivopontocerebellar Atrophy IIs, Spinocerebellar Atrophy Olivopontocerebellar Atrophy 2 Olivopontocerebellar Atrophy 2s Olivopontocerebellar Atrophy II Olivopontocerebellar Atrophy IIs Olivopontocerebellar Atrophy, Holguin Type Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 2s Spinocerebellar Ataxia with Slow Eye Movements Spinocerebellar Ataxia, Cuban Type Spinocerebellar Ataxia-2 Spinocerebellar Atrophy 2 Spinocerebellar Atrophy 2s Spinocerebellar Atrophy II Spinocerebellar Atrophy IIs Spinocerebellar Degeneration with Slow Eye Movements Swami Syndrome, Wadia Syndrome, Wadia Swami Syndrome, Wadia-Swami Type 2 Spinocerebellar Ataxia Wadia Swami Syndrome Wadia-Swami Syndrome |
| Concept UI |
M0336160 |
| Scope note | A group of 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) |
| Preferred term | Spinocerebellar Ataxia Type 7 |
| Entry term(s) |
Ataxia 7, Spinocerebellar Ataxia 7s, Spinocerebellar Atrophy III, Olivopontocerebellar Autosomal Dominant Cerebellar Ataxia, Type II OPCA with Macular Degeneration and External Ophthalmoplegia OPCA with Retinal Degeneration Olivopontocerebellar Atrophy III Olivopontocerebellar Atrophy IIIs Spinocerebellar Ataxia 7 Spinocerebellar Ataxia 7s Spinocerebellar Ataxia-7 Type 7 Spinocerebellar Ataxia |
| Concept UI |
M0336158 |
| Scope note | A group of 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) |
| Scope note | A group of 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) |
| Preferred term | Spinocerebellar Ataxia Type 5 |
| Entry term(s) |
Ataxia 5, Spinocerebellar Ataxia 5s, Spinocerebellar Spinocerebellar Ataxia 5 Spinocerebellar Ataxia 5s Spinocerebellar Ataxia-5 Type 5 Spinocerebellar Ataxia |
| Concept UI |
M0336159 |
| Scope note | A group of 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) |
| Scope note | A group of 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) |
| Preferred term | Spinocerebellar Ataxia Type 6 |
| Entry term(s) |
Ataxia 6, Spinocerebellar Ataxia 6s, Spinocerebellar Spinocerebellar Ataxia 6 Spinocerebellar Ataxia 6s Spinocerebellar Ataxia-6 Type 6 Spinocerebellar Ataxia |
| Concept UI |
M0336155 |
| Scope note | A group of 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) |
| Scope note | A group of 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) |
| Preferred term | Spinocerebellar Ataxia Type 1 |
| Entry term(s) |
Ataxia 1, Spinocerebellar Atrophy I, Olivopontocerebellar Atrophy I, Spinocerebellar Atrophy IV, Olivopontocerebellar Atrophy IVs, Olivopontocerebellar Cerebelloparenchymal Disorder I Cerebelloparenchymal Disorder Is Menzel Type OPCA OPCA, Menzel Type OPCA, Schut-Haymaker Type Olivopontocerebellar Atrophy I Olivopontocerebellar Atrophy IV Olivopontocerebellar Atrophy IVs Olivopontocerebellar Atrophy Is SCA1 SCA1s Schut Haymaker Type OPCA Schut-Haymaker Type OPCA Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 1s Spinocerebellar Ataxia-1 Spinocerebellar Atrophy I Spinocerebellar Atrophy Is Type 1 Spinocerebellar Ataxia |
| Concept UI |
M0336157 |
| Scope note | A group of 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) |
| Scope note | A group of 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) |
| Preferred term | Spinocerebellar Ataxia Type 4 |
| Entry term(s) |
Ataxia 4, Spinocerebellar Ataxia 4s, Spinocerebellar Spinocerebellar Ataxia 4 Spinocerebellar Ataxia 4s Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy Spinocerebellar Ataxia-4 Type 4 Spinocerebellar Ataxia |
| Concept UI |
M000744894 |
| Preferred term | Dominantly-Inherited Spinocerebellar Ataxias |
| Entry term(s) |
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 Ataxias, Dominantly-Inherited |
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