Friedreich's ataxia |
Ataxia with oculomotor apraxia types 1 and 2 |
Ataxia telangiectasia |
Hexosaminidase A deficiency (Tay–Sachs or Sandhoff disease) |
Adrenoleukodystrophy (X-linked) |
Cholestanolosis (cerebrotendinous xanthomatosis) |
Unverricht–Lundborg disease |
Lafora body disease |
Niemann–Pick disease type C |
Metachromatic leukodystrophy |
Abetalipoproteinaemia (Bassen–Kornzweig disease) |
Xeroderma pigmentosum, Cockayne syndrome |
Episodic ataxias (autosomal dominant) |
Neuronal ceroid lipofuscinoses (Batten's disease, Kuf's disease—autosomal dominant or recessive) |
POLG (polymerase γ) mutations |
Ataxia with isolated vitamin E deficiency |
Charlevoix–Saguenay spastic ataxia |