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Spinocerebellar ataxia
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Progressive neurological disease
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Wikipedia

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. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time. SCA is hereditary, progressive, degenerative. There is no...

Instance of
designated intractable/rare disease
class of disease
Signs and symptoms
Subclass of
hereditary ataxia
late-onset ataxia with dementia
nervous system heredodegenerative disease
eye degenerative disease
Cerebral atrophy
autosomal dominant disease
spinocerebellar degenerations
Cerebellar ataxia
Disease
References
Wikidata