G11.8
Other hereditary ataxias
Approximate Synonyms
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Dentatorubral-pallidoluysian atrophy drpla)
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Dentatorubropallidoluysian degeneration
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Primary hereditary spinocerebellar disease nondemyelinating type
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Spinocerebellar ataxia, type 1
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Spinocerebellar ataxia, type 2
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Spinocerebellar ataxia, type 3
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Spinocerebellar ataxia, type 4
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Spinocerebellar ataxia, type 5
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Spinocerebellar ataxia, type 6
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Spinocerebellar ataxia, type 7
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Spinocerebellar disease, non-demyelinating
Details
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G11.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
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The 2023 edition of ICD-10-CM G11.8 became effective on October 1, 2022.
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This is the American ICD-10-CM version of G11.8 – other international versions of ICD-10 G11.8 may differ.