Preferred Name | Spinocerebellar Ataxia | |
Synonyms |
|
|
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 |
|
createdDate |
2007-10-05 |
|
definingCitation |
Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43 |
|
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). |
|
editorial note | ||
hasBirnlexCurator | ||
hasCurationStatus | ||
hasDefinitionSource | ||
hasExternalSource | ||
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). |
|
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 |
|
synonym |
Dominantly-Inherited Spinocerebellar Ataxia Spinocerebellar Atrophy |
|
usageNote |
MeSH includes qualified subtypes |
|
subClassOf |