spinocerebellar ataxia type 20 (Q21097768)

From Wikidata
Jump to navigation Jump to search
Spinocerebellar ataxia type 20 (SCA20) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar dysarthria as the initial typical manifestation.
  • Spinocerebellar Ataxia type 20
  • Chromosome 11Q12 Duplication Syndrome, 260-Kb
  • Spinocerebellar Ataxia With Dysphonia
  • Spinocerebellar Ataxia With Spasmodic Cough
  • SCA20
  • SPINOCEREBELLAR ATAXIA 20
  • SPINOCEREBELLAR ATAXIA 20; SCA20
edit
Language Label Description Also known as
English
spinocerebellar ataxia type 20
Spinocerebellar ataxia type 20 (SCA20) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar dysarthria as the initial typical manifestation.
  • Spinocerebellar Ataxia type 20
  • Chromosome 11Q12 Duplication Syndrome, 260-Kb
  • Spinocerebellar Ataxia With Dysphonia
  • Spinocerebellar Ataxia With Spasmodic Cough
  • SCA20
  • SPINOCEREBELLAR ATAXIA 20
  • SPINOCEREBELLAR ATAXIA 20; SCA20

Statements

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit