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Spinocerebellar Ataxia Type-6
Spinocerebellar ataxia type-6
Overview
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Related in the Kosmos
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Channelopathy
Episodic ataxia
SCA13
Familial hemiplegic migraine
Genetic disorders
(16)
Spinocerebellar ataxia
DRPLA
Machado-joseph disease
Trinucleotide repeat disorders
Galactosialidosis
Galactosialidosis
Spastic ataxia
Friedreich ataxia
Spondylometaphyseal dysplasia
Spinal muscular atrophy
Fragile X
Cadasil
Myotonic dystrophy
Amelogenesis imperfecta
Episodic ataxia
SCA13
Familial hemiplegic migraine
more...
Neurological disorders
(20)
Ataxia
Cerebellar ataxia
Olivoponto- cerebellar atrophy
Dysarthria
Leukodystrophy
Leukodystrophy
Dysmetria
Subarachnoid hemorrhage
Apraxia
Neuronal ceroid lipofuscinosis
Sensory neuropathy
Spinocerebellar ataxia
DRPLA
Machado-joseph disease
Trinucleotide repeat disorders
Episodic ataxia
SCA13
Friedreich ataxia
Familial hemiplegic migraine
Fragile X
Cadasil
more...
Disability
Neurological disorders
Spinocerebellar ataxia
Dysarthria
Dysmetria
Fragile X
Myotonic dystrophy
Neurology
(8)
Movement disorders
Choreoathetosis
Dystonia
Dyskinesias
Neurological disorders
Neurological disorders
Spastic ataxia
Myotonic dystrophy
Sensory neuropathy
more...
Ion channels
CACNA1A
SCA16
Calcium channel
KCNC3
Rare diseases
Striatonigral degeneration
Amyotrophic lateral sclerosis
Galactosialidosis
Neuronal ceroid lipofuscinosis
Extrapyramidal and movement disorders
(19)
Parkinson disease
Parkinsonism
Akathisia
Blepharospasm
Choreia (disease)
Choreia (disease)
Dystonia
Essential tremor
Meige's syndrome
Movement disorders
Myoclonus
Neuroleptic malignant syndrome
Pantothenate kinase-associated neurodegeneration
Postencephalitic parkinsonism
Progressive supranuclear palsy
Restless legs syndrome
Spasmodic torticollis
Stiff person syndrome
Striatonigral degeneration
Tardive dyskinesia
more...
Vision
Physiologic nystagmus
Fixation (visual)
Saccadic
Proteins
(9)
SCA8
Ataxin 7
Ataxin 1
ATXN3
Sarcoglycan
Sarcoglycan
Tata binding protein
Frataxin
Huntingtin
Isoform
more...
Gene
(14)
Sca12
SCA14
GM2A
ATXN2
Aprataxin
Aprataxin
SPG3A
SPG11
TDP-43
DYT1
PINK1
Ataxin 1
SCA16
Tata binding protein
Frataxin
more...
Diseases and disorders
(37)
Spinocerebellar ataxia 6
Spinocerebellar ataxia 8
Spinocerebellar ataxia 1
Spinocerebellar ataxia type 3
Spinocerebellar ataxia 7
Spinocerebellar ataxia 7
Dentatorubral pallidoluysian atrophy
Anonychia onychodystrophy
Gait ataxia
Cone-rod dystrophy
Neurological disorders
Machado-joseph disease
Ataxia
Sialidosis
Galactosialidosis
Spastic ataxia
Friedreich ataxia
Spondylometaphyseal dysplasia
Spinal muscular atrophy
Olivoponto- cerebellar atrophy
Symptoms
Striatonigral degeneration
Leukodystrophy
Movement disorders
Dysmetria
Fragile X
Physiologic nystagmus
Apraxia
Cadasil
Myotonic dystrophy
Amelogenesis imperfecta
Dystonia
Neuronal ceroid lipofuscinosis
Sensory neuropathy
Dyskinesias
Parkinson disease
Rare diseases
Amyotrophic lateral sclerosis
more...
See also
(20)
Diseases and disorders
Biology
Cerebellum
Autosomal dominant
Autosomal recessive
Autosomal recessive
Sialidosis
Polyglutamine tract
Spinocerebellar
Hum. Mol. Genet.
Am. J. Hum. Genet.
Anatomy
Substantia nigra
Huntington's disease
Symptoms
Pulst
Nat. Genet.
Cerebellar diseases
X linked
NINDS
ABCA4
more...
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