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603680
ATXN8OS
ATAXIN 8 OPPOSITE STRAND
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Nervous System Diseases
Autonomic Nervous System Diseases
Primary Dysautonomias
Multiple System Atrophy
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Multiple System Atrophy
Parkinsonian Disorders
Parkinson Disease
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Dementia
Alzheimer Disease
Huntington Disease
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
Lafora Disease
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Multiple System Atrophy
Parkinsonian Disorders
Parkinson Disease
Spinal Cord Diseases
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Huntington Disease
Lafora Disease
Myotonic Dystrophy
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Multiple System Atrophy
Parkinson Disease
Tauopathies
Alzheimer Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Neuromuscular Manifestations
Muscular Atrophy
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Muscular Disorders, Atrophic
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Eye Diseases
Retinal Diseases
Retinal Degeneration
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Huntington Disease
Lafora Disease
Myotonic Dystrophy
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Muscular Dystrophies
Myotonic Dystrophy
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Friedreich Ataxia
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin E Deficiency
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neuromuscular Manifestations
Muscular Atrophy
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