- Spinocerebellar Ataxias (Genetic Forms)
- Dentatorubral-pallidoluysian atrophy (DRPLA)
- fragile X-associated tremor/ataxia syndrome (FXTAS)
- Friedreich Ataxia (FRDA)
- Ataxia-oculomotor apraxia syndrome (AOA)
- Ataxia with vitamin E deficiency (AVED)
- Marinesco Sjogren syndrome (SIL1 mutation)
- Alexanders syndrome
- Parkinsonism
- Perry syndrome
- Huntington’s disease
- Familial Parkinson’s Disease with the SNCA gene (FPD)
- Familial Parkinson’s Disease with the LRRK2 gene (FPD)
- Familial Parkinson’s Disease with the GBA gene (FPD)
- X-linked adrenoleukodystrophy (ABCD1 mutation)
- Hereditary Spastic Paraplegia (HSP)
- Hereditary Spastic Paraplegia Paraplegin (SPG7)
- Hereditary Spastic Paraplegia Mental Impairment and Thin Corpus Callosum (SPG11)
- Primary Lateral Sclerosis (PLS)
LMNB1 associated Leukodystrophy
- Mitochondriopathy
- Cerebrotendinous xanthomatosis
- Prion disease
- C9ORF72 mutation