ICD-10-CM diagnosis code
G12.8 Other spinal muscular atrophies and related syndromes
- Billable
- Yes, a complete code (FY2026)
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Other codes in G12
11 complete codes in this category.
- G12.0Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
- G12.1Other inherited spinal muscular atrophy
- G12.20Motor neuron disease, unspecified
- G12.21Amyotrophic lateral sclerosis
- G12.22Progressive bulbar palsy
- G12.23Primary lateral sclerosis
- G12.24Familial motor neuron disease
- G12.25Progressive spinal muscle atrophy
- G12.29Other motor neuron disease
- G12.8Other spinal muscular atrophies and related syndromes
- G12.9Spinal muscular atrophy, unspecified
Documentation tips
- Make sure the note supports every element of the title, “Other spinal muscular atrophies and related syndromes”: each detail in it should be traceable to the history, examination or assessment.
- Code to the highest specificity the documentation supports. If a detail is missing from the note, add it to the note rather than choosing a less specific code by default.
- Check the Tabular List and official guidelines for instructional notes (“code first”, “use additional code”, Excludes1/Excludes2) that apply to G12.
The international WHO ICD-10 also has G12.8, with its inclusion and exclusion notes; titles and detail can differ from ICD-10-CM.
ICD-10-CM is developed by the National Center for Health Statistics (NCHS), Centers for Disease Control and Prevention, U.S. Department of Health and Human Services, and is based on the WHO ICD-10. Codes and titles are reproduced unchanged from the FY2026 code list (effective 1 October 2025). Their use here does not imply endorsement by CDC, HHS or the U.S. Government. Changes effective on or after 1 October 2026 may not be reflected yet; check the current release at cdc.gov or cms.gov before submitting claims.
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