Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Nervous System Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Nervous System Diseases
Central Nervous System Diseases
Spinal Cord Diseases
Spinocerebellar Degenerations
Preferred term
Spinocerebellar Ataxias
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- Atrophies, Spinocerebellar
- Atrophy, Spinocerebellar
- Spinocerebellar Atrophies
- Spinocerebellar Atrophy
Note
- SPINOCEREBELLAR ATAXIA TYPE 3 see MACHADO-JOSEPH DISEASE is available
Scope note
- 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)
History note
- 2000; use SPINOCEREBELLAR DEGENERATION 1987-1999
In other languages
-
Finnish
-
ataxia spinocerebellaris
-
spinoserebellaarinen ataksia
-
spinoserebellaarinen atrofia
-
spinoserebellaariset atrofiat
-
Swedish
URI
http://www.yso.fi/onto/mesh/D020754
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