MeSH Treeview
Query OMIM entry list
603516
SCA10
SPINOCEREBELLAR ATAXIA 10
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Dementia
Huntington Disease
Epilepsy
Epilepsies, Partial
Epilepsy, Complex Partial
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Spinal Cord Diseases
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Myotonic Dystrophy
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Parkinson 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
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Huntington Disease
Myotonic Dystrophy
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Muscular Dystrophies
Myotonic Dystrophy
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Genomic Instability
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neuromuscular Manifestations
Muscular Atrophy
Database Center for Life Science
