G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
The ICD-10-CM code for Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] is G12.0 (FY2026). It is a billable, claim-ready diagnosis code.
Classification
- Section
- G10-G14: Systemic atrophies primarily affecting the central nervous system (G10-G14)
- Category G12
- 13 codes (11 billable)
- FY2026 Status
- Stable since FY2024
Also Known As
ICD-10-CM Alphabetic Index entries that lead to G12.0:
- Werdnig-Hoffmann syndrome (muscular atrophy)
- Syndrome › Werdnig-Hoffman
- Disease, diseased › Werdnig-Hoffmann
- Atrophy, atrophic (of) › Werdnig-Hoffmann
- Syndrome › Hoffmann-Werdnig
- Atrophy, atrophic (of) › muscle, muscular (diffuse) (general) (idiopathic) (primary) › infantile spinal
- Atrophy, atrophic (of) › muscle, muscular (diffuse) (general) (idiopathic) (primary) › spinal › infantile, type I (Werdnig-Hoffmann)
- Atrophy, atrophic (of) › muscle, muscular (diffuse) (general) (idiopathic) (primary) › progressive (bulbar) › infantile (spinal)
U.S. Hospital Utilization
- An estimated 750 U.S. inpatient stays in 2023 included G12.0 among the documented diagnoses.
Source: National Inpatient Sample (NIS), Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, 2016–2023. National survey-weighted estimates.
Official Coding Guidelines
Dominant/nondominant side (TOC entry)a. Dominant/nondominant side ................................................................................................. 45
Pain - Category G89 (TOC entry)b. Pain - Category G89.............................................................................................................. 45
Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026