Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:03685914n
Noun Concept
SYL
No term available
EN
Spinocerebellar ataxia type 13 is a rare autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, nystagmus, and ataxia of gait, stance and the limbs due to cerebellar dysfunction. Wikipedia
Relations
Sources
IS A
EN
disease
EN
rare disease
EN
spinocerebellar ataxia
GENETIC ASSOCIATION
EN
KCNC3
HEALTH SPECIALTY
EN
neurology

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License