Related MeSH Hierarchy (6)
Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Brain Diseases » Cerebellar Diseases » Cerebellar Ataxia » Spinocerebellar Ataxias
Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Brain Diseases » Cerebellar Diseases » Spinocerebellar Degenerations » Spinocerebellar Ataxias
Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Spinal Cord Diseases » Spinocerebellar Degenerations » Spinocerebellar Ataxias
Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Heredodegenerative Disorders, Nervous System » Spinocerebellar Degenerations » Spinocerebellar Ataxias
Diseases [C] » Nervous System Diseases [C10] » Neurologic Manifestations » Dyskinesias » Ataxia » Cerebellar Ataxia » Spinocerebellar Ataxias
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Heredodegenerative Disorders, Nervous System » Spinocerebellar Degenerations » Spinocerebellar Ataxias
Description
A group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) MeSH
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Subtype Terms (2)
Ataxia Telangiectasia
28 drugs (25 approved, 3 experimental)
Machado-Joseph Disease
9 drugs (3 approved, 6 experimental)
Phase 3 Indicated Drugs (2)
Phase 2 Indicated Drugs (5)
Other Experimental Indicated Drugs (2)
Organization Involved with Phase 4 Indications (2)
Organization Involved with Phase 2 Indications (12)
Organization Involved with Phase 1 Indications (2)
Organization Involved with Other Experimental Indications (5)
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UMLS Data
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