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607136
SCA17
SPINOCEREBELLAR ATAXIA 17
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Muscular Diseases
Muscle Rigidity
Muscle Spasticity
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
Creutzfeldt-Jakob Syndrome
Huntington Disease
Epilepsy
Epilepsy, Generalized
Epilepsy, Absence
Central Nervous System Infections
Prion Diseases
Creutzfeldt-Jakob Syndrome
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Dystonic Disorders
Torticollis
Parkinsonian Disorders
Parkinson Disease
Ocular Motility Disorders
Spinal Cord Diseases
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Cranial Nerve Diseases
Ocular Motility Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Huntington Disease
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Parkinson Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Dystonia
Torticollis
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Rigidity
Muscle Spasticity
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Eye Diseases
Ocular Motility Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Genetic Diseases, Inborn
Dwarfism
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Huntington Disease
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Endocrine System Diseases
Dwarfism
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Dystonia
Torticollis
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Rigidity
Muscle Spasticity
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