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183086
SCA6
SPINOCEREBELLAR ATAXIA 6
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Otorhinolaryngologic Diseases
Ear Diseases
Labyrinth Diseases
Vestibular Diseases
Vertigo
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Multiple System Atrophy
Olivopontocerebellar Atrophies
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Spinocerebellar Degenerations
Friedreich Ataxia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Headache Disorders
Headache Disorders, Primary
Migraine Disorders
Migraine with Aura
Migraine without Aura
Movement Disorders
Multiple System Atrophy
Olivopontocerebellar Atrophies
Spinal Cord Diseases
Spinocerebellar Degenerations
Friedreich Ataxia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spinocerebellar Degenerations
Friedreich Ataxia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Multiple System Atrophy
Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
Hemiplegia
Vertigo
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Ocular Motility Disorders
Nystagmus, Pathologic
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spinocerebellar Degenerations
Friedreich Ataxia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Friedreich Ataxia
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
Hemiplegia
Vertigo
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