loading...| Preferred Name | spinocerebellar ataxia | |
| Synonyms |
Spinocerebellar ataxia (disorder) spinocerebellar ataxia Spinocerebellar Atrophy Spinocerebellar Ataxias Dominantly-Inherited Spinocerebellar Ataxia |
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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://www.ebi.ac.uk/efo/EFO_0002624 |
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| comment |
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 term |
Spinocerebellar ataxia (disorder) spinocerebellar ataxia Spinocerebellar Atrophy Spinocerebellar Ataxias Dominantly-Inherited Spinocerebellar Ataxia |
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| definition source |
NIFSTD:birnlex_12648 DOID:1441 |
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| label |
spinocerebellar ataxia |
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| prefixIRI |
efo:EFO_0002624 |
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| prefLabel |
spinocerebellar ataxia |
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| see also | ||
| term editor |
Tomasz Adamusiak Ele Holloway |
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| subClassOf |