ORPHA:98757

Spinocerebellar ataxia type 3

Also called Azorean disease of the nervous system, MJD, Machado disease, Machado-Joseph disease, Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia, SCA3

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Adult, Childhood

Estimated prevalence

1-9 / 100 000 (Worldwide)

Rarity class

1-9 / 100 000

ORPHA:98757 is classified under "Neurological diseases" in the Orphanet nomenclature.