|
G11.4 |
Hereditary spastic paraplegia |
| Billable Code | is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. |
| GEMS |
| ICD-10-CM G11.4 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 334.1 Hereditary spastic paraplegia |
| ICD-10-CM G11.4is 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
|
| Type 2 Excludes |
| Cockayne's syndrome (Q87.1) |
| other disorders of purine and pyrimidine metabolism (E79.-) |
| xeroderma pigmentosum (Q82.1) |
| Alternate Description |
| Ataxia telangiectasia [Louis-Bar] |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.G11.4.' |
| Ataxia, ataxy, ataxic; hereditary; spastic |
| Ataxia, ataxy, ataxic; spastic hereditary |
| Paralysis, paralytic (complete) (incomplete); familial (recurrent) (periodic); spastic |
| Paralysis, paralytic (complete) (incomplete); spastic; familial |
| Paralysis, paralytic (complete) (incomplete); spastic; hereditary |
| Paraplegia (lower); familial spastic |
| Paraplegia (lower); hereditary, spastic |
| Paraplegia (lower); spastic; hereditary |
