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Free Medical Coding > ICD10 CM > 2025 ICD-10-CM Codes > 2025 ICD-10-CM Codes G00-G99 – Diseases of the nervous system (G00-G99) > 2025 ICD-10-CM Codes G70-G73 – Diseases of myoneural junction and muscle (G70-G73) > 2025 ICD-10-CM Codes G71 – Primary disorders of muscles (G71) > 2025 ICD-10-CM Codes G71.0 – Muscular dystrophy (G71.0) > 2025 ICD-10-CM Codes G71.03 – Limb girdle muscular dystrophies (G71.03) > 2025 ICD-10-CM Diagnosis Code G71.038 – Other limb girdle muscular dystrophy (G71.038)

2025 ICD-10-CM Diagnosis Code G71.038 – Other limb girdle muscular dystrophy (G71.038)

2024 – New Code20242025Billable/Specific Code
  • G71.038 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2024 edition of ICD-10-CM G71.038 became effective on October 1, 2022.
  • This is the American ICD-10-CM version of G71.038 – other international versions of ICD-10 G71.038 may differ.

ICD-10-CM G71.038 is grouped within Diagnostic Related Group(s):

  • 091 Other disorders of nervous system with mcc
  • 092 Other disorders of nervous system with cc
  • 093 Other disorders of nervous system without cc/mcc

Applicable To

  • LGMD R9 FKRP-related
  • LGMD R22 collagen 6-related
  • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
  • Limb girdle muscular dystrophy type 2I
  • Other autosomal recessive limb girdle muscular dystrophy

Code History

  • 2024 (effective 10/1/2022): New code
  • 2023 (effective 10/1/2022): No change
  • 2024 (effective 10/1/2023): No change
  • 2025 (effective 10/1/2024): No change

Diagnosis Index entries containing back-references to G71.038:

  • meaning Limb girdle muscular dystrophy, specified type NEC > Leyden-Möbius G71.039
  • autosomal recessive NEC > limb-girdle G71.039
  • autosomal recessive > collagen VI related G71.031
  • fukutin related protein dysfunction > due to G71.0341
  • FKRP-related autosomal recessive > limb-girdle G71.039
  • R7 (autosomal recessive) > limb-girdle G71.039
  • R8 (autosomal recessive) > limb-girdle G71.039
  • R9 (autosomal recessive) > limb-girdle G71.039
  • R10 (autosomal recessive) > limb-girdle G71.039
  • R11 (autosomal recessive) > limb-girdle G71.039
  • R13 (autosomal recessive) > limb-girdle G71.039
  • R14 (autosomal recessive) > limb-girdle G71.039
  • R15 (autosomal recessive) > limb-girdle G71.039
  • R16 (autosomal recessive) > limb-girdle G71.039
  • R17 (autosomal recessive) > limb-girdle G71.039
  • R18 (autosomal recessive) > limb-girdle G71.039
  • R19 (autosomal recessive) > limb-girdle G71.039
  • R20 (autosomal recessive) > limb-girdle G71.039
  • R21 (autosomal recessive) > limb-girdle G71.039
  • R22 (autosomal recessive) > limb-girdle G71.039
  • R23 (autosomal recessive) > limb-girdle G71.039
  • R24 (autosomal recessive) > limb-girdle G71.039
  • type 2 (autosomal recessive) > limb-girdle G71.039
  • specified NEC > type 2 (autosomal recessive) G71.038
  • type 2I (autosomal recessive) > limb-girdle G71.039

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