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Related to spinocerebellar disorder: Spinocerebellar ataxia
an inherited disorder characterized by a progressive degeneration of the spinal cord and cerebellum, often involving other parts of the nervous system as well. These disorders tend to occur within families and can be inherited as dominant or recessive traits. Onset is usually early, during childhood or adolescence. No effective treatment is known. Some kinds of spinocerebellar degeneration are ataxia-telangiectasia syndrome, Charcot-Marie-Tooth disease, Dejerine-Sottas disease, Friedreich's ataxia, olivopontocerebellar atrophy, and Refsum's syndrome.