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Neuroscience Information Framework (NIF) Standard Ontology
Last uploaded:
February 10, 2018
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Id | http://uri.neuinfo.org/nif/nifstd/birnlex_12648
http://uri.neuinfo.org/nif/nifstd/birnlex_12648
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Preferred Name | Spinocerebellar Ataxia |
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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Synonyms |
Dominantly-Inherited Spinocerebellar Ataxia
Spinocerebellar Atrophy
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Obsolete | true |
Type | http://www.w3.org/2002/07/owl#Class |
All Properties
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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alternative label |
Dominantly-Inherited Spinocerebellar Ataxia
Spinocerebellar Atrophy
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preferred label |
Spinocerebellar Ataxia
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label |
Spinocerebellar Ataxia
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externalSourceId |
D020754
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synonym |
Dominantly-Inherited Spinocerebellar Ataxia
Spinocerebellar Atrophy
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hasExternalSource | |
createdDate |
October 5, 2007
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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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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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See less
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usageNote |
MeSH includes qualified subtypes
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definingCitationURI | |
hasCurationStatus | |
MeshUid |
D020754
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subClassOf | |
hasDefinitionSource | |
Resource Identifier |
D020754
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hasBirnlexCurator | |
editorial note | |
owl:deprecated |
true
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type | |
modifiedDate |
October 5, 2007
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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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