Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01616637n
Noun Concept
Categories: Rare diseases, Systemic atrophies primarily affecting the central nervous system, Cytoskeletal defects, Neurodegenerative disorders, Autosomal dominant disorders
EN
spinocerebellar ataxia  Spinocerebellar Atrophy  ADCA  autosomal dominant cerebellar ataxia  Autosomal dominant spinocerebellar ataxia
EN
Spinocerebellar ataxia is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. Wikipedia
Definitions
Relations
Sources
EN
Spinocerebellar ataxia is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. Wikipedia
A neurological condition Wikipedia Disambiguation
Group of dominantly inherited, predominately late-onset, cerebellar ataxias. Neuro-developmental outcome and brain-derived neurotrophic factor level in relation to feeding practice in early infancy. Wikidata
IS A
cerebral atrophy
cerebellar ataxia
hereditary ataxia
HAS KIND
dentatorubral-pallidoluysian atrophy
Machado-Joseph disease
Erythrokeratodermia with ataxia
spinocerebellar ataxia type 13
spinocerebellar ataxia with epilepsy
+4 relations
HEALTH SPECIALTY
neurology
Wikipedia
EN
spinocerebellar ataxia
Wikidata
EN
spinocerebellar ataxia
Wikipedia Redirections
EN
infantile onset spinocerebellar ataxia, Ohaha syndrome, Ophthalmoplegia ataxia hypoacusis, Spinal cerebellar atrophy, Spino-cerebellar Ataxia, Spinocerebellar Ataxia, Spinocerebellar ataxia 5, Spinocerebellar ataxia dysmorphism, spinocerebellar ataxias, Spinocerebellar Atrophy, Spinocerebellar atrophy, spinocerebellar degeneration, spinocerebellar degenerations, X-linked recessive spinocerebellar ataxia
Wikidata Alias
EN
ADCA, autosomal dominant cerebellar ataxia, Autosomal dominant spinocerebellar ataxia, cerebellar ataxia, autosomal dominant, spinocerebellar ataxias

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