|
G11.0 |
Congenital nonprogressive 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 G11.0 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 334.2 Primary cerebellar degeneration |
| ICD-10-CM G11.0is grouped within Diagnostic Related Group(s) (MS-DRG v30.0) |
| 58 MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH MCC
|
| 59 MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH CC
|
| 60 MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITHOUT CC/MCC
|
| Alternate Description |
| Huntington's chorea |
| Huntington's dementia |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.G11.0.' |
| Ataxia, ataxy, ataxic; congenital nonprogressive |
| Ataxia, ataxy, ataxic; nonprogressive, congenital |
