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Select a gene for your disease of interest:
Spinocerebellar ataxia (ATX)
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
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
Spinocerebellar ataxia
ANO10
Primary familial brain calcification (PFBC) - 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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