loading...| Preferred Name | Spinocerebellar Ataxia | |
| Synonyms |
Dominantly-Inherited Spinocerebellar Ataxia|Spinocerebellar Atrophy |
|
| ID |
http://bioontology.org/projects/ontologies/birnlex#birnlex_12648 |
|
| abbrev | ||
| class_or_indiv |
true |
|
| 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). |
|
| external_id_urls |
http://www.nlm.nih.gov/cgi/mesh/2008/MB_cgi?field=uid&term=D020754 |
|
| external_ids |
meshUID:D020754 |
|
| label |
Spinocerebellar Ataxia |
|
| mod_date |
2007-10-05 |
|
| preferred_label |
Spinocerebellar Ataxia |
|
| prefixIRI |
birnlex_12648 |
|
| prefLabel |
Spinocerebellar Ataxia |
|
| retired |
false |
|
| synonyms |
Dominantly-Inherited Spinocerebellar Ataxia|Spinocerebellar Atrophy |
|
| subClassOf |
http://bioontology.org/projects/ontologies/birnlex#birnlex_12647 |