ICD-10-CM Code G71: Primary disorders of muscles and Related Diagnosis Codes.


The ICD-10-CM (the International Classification of Diseases, Tenth Revision, Clinical Modification) is a standardized coding system used when classifying diseases and medical conditions. Healthcare providers report these codes on Medical claims when diagnosing patient care.

Explore ICD-10-CM codes, organized by chapters based on body systems and medical conditions, as outlined in the International Classification of Diseases, Tenth Revision, Clinical Modification.

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A categorized list of ICD-10-CM codes organized by chapters based on body systems or medical conditions, according to the International Classification of Diseases, Tenth Revision, Clinical Modification.

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  • G71 - Primary disorders of muscles
    • G71.0 - Muscular dystrophy
      • G71.00 - Muscular dystrophy, unspecified
      • G71.01 - Duchenne or Becker muscular dystrophy
      • G71.02 - Facioscapulohumeral muscular dystrophy
      • G71.03 - Limb girdle muscular dystrophies
        • G71.031 - Autosomal dominant limb girdle muscular dystrophy
        • G71.032 - Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
        • G71.033 - Limb girdle muscular dystrophy due to dysferlin dysfunction
        • G71.034 - Limb girdle muscular dystrophy due to sarcoglycan dysfunction
          • G71.0340 - Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
          • G71.0341 - Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
          • G71.0342 - Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
          • G71.0349 - Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
        • G71.035 - Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
        • G71.038 - Other limb girdle muscular dystrophy
        • G71.039 - Limb girdle muscular dystrophy, unspecified
      • G71.09 - Other specified muscular dystrophies
    • G71.1 - Myotonic disorders
      • G71.11 - Myotonic muscular dystrophy
      • G71.12 - Myotonia congenita
      • G71.13 - Myotonic chondrodystrophy
      • G71.14 - Drug induced myotonia
      • G71.19 - Other specified myotonic disorders
    • G71.2 - Congenital myopathies
      • G71.20 - Congenital myopathy, unspecified
      • G71.21 - Nemaline myopathy
      • G71.22 - Centronuclear myopathy
        • G71.220 - X-linked myotubular myopathy
        • G71.228 - Other centronuclear myopathy
      • G71.29 - Other congenital myopathy
    • G71.3 - Mitochondrial myopathy, not elsewhere classified
    • G71.8 - Other primary disorders of muscles
    • G71.9 - Primary disorder of muscle, unspecified

Note: The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes are developed and maintained by the Centers for Disease Control and Prevention (CDC). CDC's National Center for Health Statistics (NCHS) is responsible for the clinical modification of ICD-10 for use in the United States. The World Health Organization (WHO), which owns and publishes ICD-10, authorized NCHS to develop ICD-10-CM. All modifications to ICD-10 must conform to WHO's established ICD structure and conventions. All rights are reserved by the respective entities.