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G11.2 |
Late-onset cerebellar ataxia |
| Billable Code | is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. |
| GEMS |
| ICD-10-CM G11.2 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 334.2 Primary cerebellar degeneration |
| ICD-10-CM G11.2is grouped within Diagnostic Related Group(s) (MS-DRG v30.0) |
| 58 MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH MCC
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| 59 MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH CC
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| 60 MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITHOUT CC/MCC
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| Alternate Description |
| Early-onset cerebellar ataxia with essential tremor |
| Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia] |
| Early-onset cerebellar ataxia with retained tendon reflexes |
| Friedreich's ataxia (autosomal recessive) |
| X-linked recessive spinocerebellar ataxia |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.G11.2.' |
| Ataxia, ataxy, ataxic; cerebellar (hereditary); late-onset (Marie's) |
| Ataxia, ataxy, ataxic; Marie's (cerebellar) (heredofamilial) (late- onset) |
| Ataxia, ataxy, ataxic; Sanger-Brown's (hereditary) |
| Marie's; cerebellar ataxia (late-onset) |
| Sanger-Brown ataxia |
