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Preferred Name

Spinocerebellar Ataxia
Synonyms

Dominantly-Inherited Spinocerebellar Ataxia

Spinocerebellar Atrophy
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).
ID

http://uri.neuinfo.org/nif/nifstd/birnlex_12648
Obsolete

true
alternative label

Dominantly-Inherited Spinocerebellar Ataxia

Spinocerebellar Atrophy
createdDate

2007-10-05
definingCitation

Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43
definingCitationURI

http://www.ninds.nih.gov/disorders/ataxia/ataxia.htm
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).
editorial note

http://uri.neuinfo.org/nif/nifstd/readable/uncurated
externalSourceId

D020754
hasBirnlexCurator

http://uri.neuinfo.org/nif/nifstd/readable/Bill_Bug
hasCurationStatus

http://uri.neuinfo.org/nif/nifstd/readable/uncurated
hasDefinitionSource

http://uri.neuinfo.org/nif/nifstd/readable/MeSH_defSource
hasExternalSource

http://uri.neuinfo.org/nif/nifstd/readable/MeSH
label

Spinocerebellar Ataxia
MeshUid

D020754
modifiedDate

2007-10-05
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).

http://uri.neuinfo.org/nif/nifstd/readable/uncurated
owl:deprecated

true
preferred label

Spinocerebellar Ataxia
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
Resource Identifier

D020754
synonym

Dominantly-Inherited Spinocerebellar Ataxia

Spinocerebellar Atrophy
usageNote

MeSH includes qualified subtypes
subClassOf

http://uri.neuinfo.org/nif/nifstd/birnlex_12647
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