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Machado-joseph Disease
Machado-Joseph disease
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Neurological disorders
(16)
Spinocerebellar ataxia
Spinocerebellar ataxia type-6
DRPLA
Trinucleotide repeat disorders
Episodic ataxia
Episodic ataxia
Dysarthria
Progressive sclerosing poliodystrophy
Hereditary sensory and autonomic neuropathies
Olfaction disorders
Meckel-Gruber syndrome
Alzheimer's disease
Friedreich ataxia
Charcot-Marie Tooth Disease
Fragile X
Olivoponto- cerebellar atrophy
Neurodegenerative disease
more...
Genetic disorders
(19)
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Fukuyama type muscular dystrophy
Leukodystrophy, globoid cell
Galactosemias
Galactosemias
Galactosialidosis
Multiple sulfatase deficiency
Spastic ataxia
Spinal muscular atrophy
Spinocerebellar ataxia
Spinocerebellar ataxia type-6
DRPLA
Trinucleotide repeat disorders
Episodic ataxia
Hereditary sensory and autonomic neuropathies
Meckel-Gruber syndrome
Friedreich ataxia
Charcot-Marie Tooth Disease
Fragile X
more...
Diseases and disorders
(59)
Joseph disease
Spinocerebellar ataxia type 3
Spinocerebellar ataxia 3
Azorean disease
Morvan disease
Morvan disease
Postpoliomyelitis syndrome
Glossopharyngeal nerve diseases
Male turner syndrome
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Marinesco sjogren syndrome
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Encephalitis, arbovirus
Dystonia
Intervertebral disk displacement
Rosenthal syndrome
Multiple hamartoma syndrome
Metatropic dwarfism
Sialidosis
Striatonigral degeneration
Brachial plexus neuropathies
Phytanic acid storage disease
Optic neuropathy, ischemic
X-linked hypophosphatemic rickets
Moersch-woltmann syndrome
Mayer-Roki- tansky-Kuster-Hauser syndrome
Malignant atrophic papulosis
Temporal arteritis
Dentatorubral pallidoluysian atrophy
Miller fisher syndrome
Myoclonus
Meige syndrome
Myotubular myopathy
Fasciculations
Myelodysplastic syndromes
Melorheostosis
Neurological disorders
Hyperostosis, cortical, congenital
Fukuyama type muscular dystrophy
Progressive sclerosing poliodystrophy
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Olfaction disorders
Galactosemias
Galactosialidosis
Multiple sulfatase deficiency
Alzheimer's disease
Spastic ataxia
Friedreich ataxia
Spinal muscular atrophy
Charcot-Marie Tooth Disease
Fragile X
Olivoponto- cerebellar atrophy
more...
Disability
Spasticity
Spinocerebellar ataxia
Neurological disorders
Dysarthria
Fragile X
Neurology
(11)
Myoclonic Encephalopathy of infants
Acquired epileptiform aphasia
Postural instability
Neurological disorders
Adrenoleuk- odystrophy
Adrenoleuk- odystrophy
Dystonia
Temporal arteritis
Spastic ataxia
Miller fisher syndrome
Meige syndrome
Neurodegenerative disease
more...
Motor neuron disease
(11)
Hirayama syndrome
ALS Association
ALS Society of Canada
Amyotrophic lateral sclerosis
Motor neurone disease
Motor neurone disease
People with motor neuron disease
Postpoliomyelitis syndrome
Primary lateral sclerosis
Spinal muscular atrophy
Split hand syndrome
Survival motor neuron spinal muscular atrophy
more...
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Leukodystrophy, globoid cell
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Central nervous system
Cerebellar
Spinocerebellar
Extrapyramidal
Neurodegenerative disease
Extrapyramidal and movement disorders
(19)
Parkinsonism
Akathisia
Blepharospasm
Choreia (disease)
Dystonia
Dystonia
Essential tremor
Meige syndrome
Movement disorder
Myoclonus
Neuroleptic malignant syndrome
Pantothenate kinase-associated neurodegeneration
Parkinson's disease
Postencephalitic parkinsonism
Progressive supranuclear palsy
Restless legs syndrome
Spasmodic torticollis
Stiff person syndrome
Striatonigral degeneration
Tardive dyskinesia
more...
See also
(20)
Ataxin-3
Azorean
GM2A
Autosomal dominant
SCA8
SCA8
Sensorimotor
Human Molecular Genetics
Familial Alzheimer disease
NINDS
Macrencephaly
Ataxin 7
Muscle atrophy
Mycosis fungoides
Dominating decision rule
Mullerian duct
Groote Eylandt
Alicia Machado
Machiavelian
CACNA1A
Muscle Disease
more...
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