G11.0 - Congenital nonprogressive ataxia
The ICD 10 Code for Congenital nonprogressive ataxia is listed as G11.0.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.
| ICD 10 CM Field | Value |
|---|---|
| Diagnosis Code: | G11.0
|
| Description: | Congenital nonprogressive ataxia |
| Diagnostic Related Groups
(MS-DRG v30.0) |
058 - Multiple Sclerosis & Cerebellar Ataxia W Mcc
059 - Multiple Sclerosis & Cerebellar Ataxia W Cc 060 - Multiple Sclerosis & Cerebellar Ataxia W/o Cc/mcc |
| Chapter | Diseases of the nervous system (G00-G99) |
| Block | Systemic atrophies primarily affecting the central nervous system (G10-G14) |
| Parent | G11 - Hereditary ataxia |
| ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD 9 Dx Code: | 334.2 - Primary cerebellar degeneration (approximate) |
| ICD-10-CM Siblings (same level / similar specificity) of G11.0: | |
| G11.1 - Early-onset cerebellar ataxia | |
| G11.2 - Late-onset cerebellar ataxia | |
| G11.3 - Cerebellar ataxia with defective DNA repair | |
| G11.4 - Hereditary spastic paraplegia | |
| G11.8 - Other hereditary ataxias | |
| G11.9 - Hereditary ataxia, unspecified | |