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Concept information

disease > genetic disease > hereditary disease > spinocerebellar ataxia
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > ataxia > cerebellar ataxia > spinocerebellar ataxia
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > spinocerebellar ataxia
... > disease > striated muscle disease > dystonia > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > spinocerebellar ataxia
... > disease > nervous system diseases > neurological disorder > involuntary movement > dystonia > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > spinocerebellar ataxia
... > disease > nervous system diseases > neurological disorder > involuntary movement > extrapyramidal syndrome > dyskinesia > ataxia > cerebellar ataxia > spinocerebellar ataxia
... > disease > nervous system diseases > neurological disorder > involuntary movement > dyskinesia > ataxia > cerebellar ataxia > spinocerebellar ataxia
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > cerebellar disease > cerebellar ataxia > spinocerebellar ataxia
disease > degenerative disease > spinocerebellar ataxia

Terme préférentiel

spinocerebellar ataxia  

Définition

  • Spinocerebellar ataxia (SCA), is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-JTSMWJJB-7

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