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Select a gene for your disease of interest:
Spinocerebellar ataxia (ATX)
ANO10
TBP
Chorea (CHOR)
ADCY5
NKX2-1
PDE10A
Dystonia (DYT)
Isolated dystonia
ANO3
AOPEP
EIF2AK2
GNAL
HPCA
KMT2B
PRKRA
THAP1
TOR1A
VPS16
Combined dystonia (Myoclonus-dystonia)
KCTD17
SGCE
Dystonia/Parkinsonism (DYT/PARK)
Dopa-responsive dystonia
GCH1
PTS
QDPR
SPR
TH
X-linked dystonia-parkinsonism
TAF1
Other forms of dystonia-parkinsonism
CP
GLB1
PLA2G6
SLC30A10
SLC6A3
Rapid-onset dystonia-parkinsonism
ATP1A3
in progress
Hereditary spastic paraplegia (HSP)
ATL1
REEP1
SPAST
Parkinsonism (PARK)
Classical parkinsonism, dominant forms
LRRK2
SNCA
VPS35
RAB32
Early-onset parkinsonism, recessive forms
PARK7
PRKN
PINK1
GBA1-related parkinsonism
GBA1
Atypical parkinsonism
ATP13A2
DCTN1
DNAJC6
FBXO7
SYNJ1
VPS13C
Paroxysmal movement disorder (PxMD)
Episodic ataxia
CACNA1A
KCNA1
PDHA1
SLC1A3
Paroxysmal dyskinesia
PNKD
PRRT2
SLC2A1
Primary brain calcification (PBC) - associated movement disorder
JAM2
MYORG
PDGFB
PDGFRB
SLC20A2
XPR1
© University of Lübeck. Last updated on
Dec. 2, 2020. Version: 3.5.95
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