Select a gene for your disease of interest:

Spinocerebellar ataxia (ATX)
TBP in progress
Chorea (CHOR)
Dystonia (DYT)
Dystonia/Parkinsonism (DYT/PARK)
GCH1 GLB1 PTS SLC30A10 SLC6A3 SPR TAF1 TH ATP1A3 in progress CP in progress PLA2G6 in progress
Hereditary spastic paraplegia (HSP)
REEP1 SPAST in progress ATL1 in progress
Parkinsonism (PARK)
Classical Parkinsonism, dominant forms
Early-onset Parkinsonism, recessive forms
Atypical Parkinsonism
Paroxysmal movement disorder (PxMD)
Episodic ataxia
KCNA1 PDHA1 SLC1A3 CACNA1A in progress
Paroxysmal dyskinesia
Primary familial brain calcification (PFBC) - associated movement disorder
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