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607047
ATXN3
ATAXIN 3
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Machado-Joseph Disease
Dementia
Huntington Disease
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Spinal Cord Diseases
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Machado-Joseph Disease
Demyelinating Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Machado-Joseph Disease
Parkinson Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Heredodegenerative Disorders, Nervous System
Huntington Disease
Mental Retardation, X-Linked
Fragile X Syndrome
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Machado-Joseph Disease
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Genomic Instability
Nerve Degeneration
Database Center for Life Science
