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Neuroscience Information Framework (NIF) Dysfunction Ontlogy
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April 11, 2018
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Preferred Name | Spinocerebellar Ataxia | |
Synonyms |
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Definitions |
A group of dominantly inherited, predominatly 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 (MeSH). |
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ID |
http://uri.neuinfo.org/nif/nifstd/birnlex_12648 |
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createdDate |
2007-10-05
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definingCitation |
Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43
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definingCitationURI | ||
definition |
A group of dominantly inherited, predominatly 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 (MeSH).
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editorial note | ||
hasBirnlexCurator | ||
hasCurationStatus | ||
hasDefinitionSource | ||
hasExternalSource | ||
label |
Spinocerebellar Ataxia
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MeshUid |
D020754
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modifiedDate |
2007-10-05
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note |
A group of dominantly inherited, predominatly 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 (MeSH).
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preferred label |
Spinocerebellar Ataxia
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putativeClassExtension |
Spinocerebellar Ataxia Type 2 Spinocerebellar Ataxia Type 1 Spinocerebellar Ataxia Type 5 Spinocerebellar Ataxia Type 6 Spinocerebellar Ataxia Type 7 Spinocerebellar Ataxia Type 4
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synonym |
Dominantly-Inherited Spinocerebellar Ataxia Spinocerebellar Atrophy
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usageNote |
MeSH includes qualified subtypes
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subClassOf |
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