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Spinocerebellar Ataxia Type-13
Spinocerebellar ataxia type-13
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Channelopathy
Spinocerebellar ataxia type-6
Episodic ataxia
Familial hemiplegic migraine
Neurological disorders
(17)
Spinocerebellar ataxia
Hereditary sensory and autonomic neuropathies
Machado-joseph disease
DRPLA
Olfaction disorders
Olfaction disorders
Ataxia
Trinucleotide repeat disorders
Friedreich ataxia
Dysarthria
Spinal and bulbar muscular atrophy
Olivoponto- cerebellar atrophy
Cadasil
Sensory neuropathy
Charcot marie tooth
Spinocerebellar ataxia type-6
Episodic ataxia
Familial hemiplegic migraine
more...
Genetic disorders
(20)
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Leukodystrophy, globoid cell
Spastic ataxia
Galactosemias
Galactosemias
Spondyloep- imetaphyseal dysplasia
Spinal muscular atrophy
Joubert syndrome
Spinocerebellar ataxia
Spinocerebellar ataxia type-6
Hereditary sensory and autonomic neuropathies
Machado-joseph disease
DRPLA
Episodic ataxia
Trinucleotide repeat disorders
Friedreich ataxia
Spinal and bulbar muscular atrophy
Cadasil
Familial hemiplegic migraine
Charcot marie tooth
more...
Neurology
(9)
Limb girdle muscular dystrophy
Dystonia
Archives of Neurology
Nerve damage
Neurological disorders
Neurological disorders
Adrenoleuk- odystrophy
Spastic ataxia
Sensory neuropathy
Joubert syndrome
more...
Disability
Neurological disorders
Spinocerebellar ataxia
Dysarthria
Spinal and bulbar muscular atrophy
Ion channels
KCNC3
CACNA1A
SCA16
Calcium channel
Voltage-gated
Autoimmune diseases
Purpura, schoenlein-henoch
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Motor neuron disease
(11)
Amyotrophic lateral sclerosis
Postpoliomyelitis syndrome
ALS Association
ALS Society of Canada
Monomelic amyotrophy
Monomelic amyotrophy
Motor neurone disease
People with motor neuron disease
Primary lateral sclerosis
Spinal muscular atrophy
Split hand syndrome
Survival motor neuron spinal muscular atrophy
more...
Vitamins
Tocotrienols
Tocopherols
Tocopheryl acetate
Gamma-tocopherol
Health
Diseases and disorders
Symptoms
Anatomy
Proteins
SCA8
Ataxin 7
Ataxin
ATXN1
Gene
(9)
Sca12
ATXN2
SCA14
SPG11
SPG3A
SPG3A
TDP-43
PINK1
ATXN1
SCA16
more...
Diseases and disorders
(46)
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Encephalitis, arbovirus
Intervertebral disk displacement
Spinocerebellar ataxia 2
Rosenthal syndrome
Brachial plexus neuropathies
Spinocerebellar ataxia type 3
Spinocerebellar ataxia 1
Myotonic dystrophy type 2
Rare diseases
Neurological disorders
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Machado-joseph disease
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Olfaction disorders
Symptoms
Ataxia
Spastic ataxia
Galactosemias
Optic neuropathy, ischemic
Friedreich ataxia
Spondyloep- imetaphyseal dysplasia
Spinal muscular atrophy
Spinal and bulbar muscular atrophy
Olivoponto- cerebellar atrophy
Cadasil
Sensory neuropathy
Cone-rod dystrophy
Leber congenital amaurosis
Amyotrophic lateral sclerosis
Limb girdle muscular dystrophy
Joubert syndrome
Dystonia
Charcot marie tooth
Multiple system atrophy
more...
See also
(20)
Cerebellar
Fetofetal transfusion
Autosomal dominant
Autosomal recessive
Optic neuropathy, ischemic
Optic neuropathy, ischemic
Hum. Mol. Genet.
Am. J. Hum. Genet.
OMIM
Spinocerebellar
Nature Genetics
Pulst
ABCA4
Racemic
NINDS
X linked
Interictal
Mov. Disord.
Ann. Neurol.
Wild type
Cone-rod dystrophy
more...
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