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ICD-10-CM Diagnosis Code G12.0

Effective Date: 10/01/2015 To 09/30/2025

Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

CMS-HCC-V24 CMS-HCC-V28 RxHCC Age Gender Maternity Acute or Chronic MCC
72 190 155 -- -- -- Acute No
Back-references to G12.0
  • Atrophy, atrophic(of)
    • Werdnig-Hoffmann G12.0
      • muscle, muscular(diffuse) (general) (idiopathic) (primary) M62.50
        • infantile spinal G12.0
          • progressive(bulbar) G12.21
            • infantile(spinal) G12.0
              • spinal G12.25
                • infantile G12.0
              • spinal G12.9
                • infantile, type I(Werdnig-Hoffmann) G12.0
            • Disease, diseased see also Syndrome
              • Werdnig-Hoffmann G12.0
              • Syndrome see also Disease
                • Hoffmann-Werdnig G12.0
                  • Werdnig-Hoffman G12.0
                  • Werdnig-Hoffmann syndrome(muscular atrophy) G12.0
                  • Related Medications for G12.0
                    • nusinersen

                    Chapter, Section and Diagnosis Prefix for G12.0
                      G00-G99 :

                      Diseases of the nervous system

                      G10-G14 :

                      Systemic atrophies primarily affecting the central nervous system

                      G12 :

                      Spinal muscular atrophy and related syndromes