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ICD-10-CM Diagnosis Code G71.031

Effective Date: 10/01/2022 To 09/30/2025

Autosomal dominant limb girdle muscular dystrophy

CMS-HCC-V24 CMS-HCC-V28 RxHCC Age Gender Maternity Acute or Chronic MCC
76 197 -- -- -- -- Acute No
Applicable To for G71.031:
  • LGMD D4 calpain-3-related

  • LGMD D5 collagen 6-related

  • Limb girdle muscular dystrophy type 1

Back-references to G71.031
  • Calpainopathy(primary) G71.032
    • autosomal dominant G71.031
    • Dystrophy, dystrophia
      • muscular G71.00
        • limb-girdle G71.039
          • D1(autosomal dominant) G71.031
            • D2(autosomal dominant) G71.031
              • D3(autosomal dominant) G71.031
                • D4(autosomal dominant) G71.031
                  • D5(autosomal dominant) G71.031
                    • calpain-3-related G71.032
                      • autosomal dominant G71.031
                      • collagen VI related
                        • autosomal dominant G71.031
                        • type 1(autosomal dominant) G71.031
                          • type 1A(autosomal dominant) G71.031
                            • type 1B(autosomal dominant) G71.031
                              • type 1C(autosomal dominant) G71.031
                                • type 1E(autosomal dominant) G71.031
                                  • type 1H(autosomal dominant) G71.031
                                    • type 1I(autosomal dominant) G71.031
                                • Chapter, Section and Diagnosis Prefix for G71.031
                                    G00-G99 :

                                    Diseases of the nervous system

                                    G70-G73 :

                                    Diseases of myoneural junction and muscle

                                    G71 :

                                    Primary disorders of muscles