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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Spinocerebellar Ataxias [Disease/Finding] | |
| Synonyms |
Spinocerebellar Ataxias, Dominantly-Inherited Dominantly-Inherited Spinocerebellar Ataxias Spinocerebellar Atrophies Spinocerebellar Ataxias |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000004172 |
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| altLabel |
Spinocerebellar Ataxias, Dominantly-Inherited Dominantly-Inherited Spinocerebellar Ataxias Spinocerebellar Atrophies Spinocerebellar Ataxias
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| cui |
C0087012
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| MESH DEFINITION |
A group of dominantly inherited, predominately 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. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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| MESH DUI |
D020754
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| MeSH name |
Spinocerebellar Ataxias
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| MESH UI |
M0020337
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| NDFRT kind |
DISEASE_KIND
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| notation |
N0000004172
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| NUI |
N0000004172
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|
| prefLabel |
Spinocerebellar Ataxias [Disease/Finding]
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| SNOMED CID |
129609000
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| tui |
T047
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| subClassOf |
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