loading...| Preferred Name |
Spinocerebellar Ataxias [Disease/Finding] |
|
| Synonyms |
Spinocerebellar Ataxias, Dominantly-Inherited Spinocerebellar Ataxias |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000004172 |
|
| altLabel |
Spinocerebellar Ataxias, Dominantly-Inherited Dominantly-Inherited Spinocerebellar Ataxias Spinocerebellar Atrophies Spinocerebellar Ataxias |
|
| cui |
C0087012 |
|
| 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) |
|
| MESH DUI |
D020754 |
|
| MeSH name |
Spinocerebellar Ataxias |
|
| MESH UI |
M0020337 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000004172 |
|
| NUI |
N0000004172 |
|
| prefLabel |
Spinocerebellar Ataxias [Disease/Finding] |
|
| SNOMED CID |
129609000 |
|
| tui |
T047 |
|
| subClassOf |