ORPHA:1955

Spinocerebellar ataxia type 34

Also called Erythrokeratodermia with ataxia, SCA34, Spinocerebellar ataxia and erythrokeratodermia

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Adolescent, Adult, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:1955 is classified under "Neurological diseases" in the Orphanet nomenclature.