G12.0 - Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
The ICD 10 Code for Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] is listed as G12.0.
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: | G12.0
|
| Description: | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] |
| Diagnostic Related Groups
(MS-DRG v30.0) |
056 - Degenerative Nervous System Disorders W Mcc
057 - Degenerative Nervous System Disorders W/o Mcc |
| Chapter | Diseases of the nervous system (G00-G99) |
| Block | Systemic atrophies primarily affecting the central nervous system (G10-G14) |
| Parent | G12 - Spinal muscular atrophy and related syndromes |
| ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD 9 Dx Code: | 335.0 - Werdnig-Hoffmann disease |
| ICD-10-CM Siblings (same level / similar specificity) of G12.0: | |
| G12.1 - Other inherited spinal muscular atrophy | |
| G12.2 - Motor neuron disease | |
| G12.8 - Other spinal muscular atrophies and related syndromes | |
| G12.9 - Spinal muscular atrophy, unspecified | |