18 result found:

Primary disorders of muscles
ICD-10-CM Diagnosis Code G71
  • G71 Primary disorders of muscles
    • G71.0 Muscular dystrophy
      • G71.00 …… unspecified
      • G71.01 Duchenne or Becker muscular dystrophy
      • G71.02 Facioscapulohumeral muscular dystrophy
      • 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 classif...
    • G71.8 Other primary disorders of muscles
    • G71.9 Primary disorder of muscle, unspecified
Muscular dystrophy
ICD-10-CM Diagnosis Code G71.0

Muscular dystrophy

    2016 2017 2018 2019 - Converted to Parent Code 2020 2021 2022 Non-Billable/Non-Specific Code
Myotonic disorders
ICD-10-CM Diagnosis Code G71.1

Myotonic disorders

    2016 2017 2018 2019 2020 2021 2022 Non-Billable/Non-Specific Code
Congenital myopathies
ICD-10-CM Diagnosis Code G71.2

Congenital myopathies

    2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 Non-Billable/Non-Specific Code
Type 2 Excludes
  • arthrogryposis multiplex congenita (Q74.3)
Mitochondrial myopathy, not elsewhere classified
ICD-10-CM Diagnosis Code G71.3

Mitochondrial myopathy, not elsewhere classified

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Type 1 Excludes
  • Kearns-Sayre syndrome (H49.81)
  • Leber's disease (H47.21)
  • Leigh's encephalopathy (G31.82)
  • mitochondrial metabolism disorders (E88.4.-)
  • Reye's syndrome (G93.7)
Other primary disorders of muscles
ICD-10-CM Diagnosis Code G71.8

Other primary disorders of muscles

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Primary disorder of muscle, unspecified
ICD-10-CM Diagnosis Code G71.9

Primary disorder of muscle, unspecified

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
  • Hereditary myopathy NOS
Sarcopenia
underlying disease, if applicable, such as:; disorders of myoneural junction and muscle disease in diseases classified elsewhere (G73.-); other and unspecified myopathies (G72.-); primary disorders of muscles (G71.-); Age-related sarcopenia
ICD-10-CM Diagnosis Code M62.84

Sarcopenia

    2017 - New Code 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
  • Age-related sarcopenia
Code First
  • underlying disease, if applicable, such as:
  • disorders of myoneural junction and muscle disease in diseases classified elsewhere (G73.-)
  • other and unspecified myopathies (G72.-)
  • primary disorders of muscles (G71.-)
Muscular dystrophy, unspecified
ICD-10-CM Diagnosis Code G71.00

Muscular dystrophy, unspecified

    2019 - New Code 2020 2021 2022 Billable/Specific Code
Duchenne or Becker muscular dystrophy
ICD-10-CM Diagnosis Code G71.01

Duchenne or Becker muscular dystrophy

    2019 - New Code 2020 2021 2022 Billable/Specific Code
Applicable To
  • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
  • Benign [Becker] muscular dystrophy
  • Severe [Duchenne] muscular dystrophy
Facioscapulohumeral muscular dystrophy
ICD-10-CM Diagnosis Code G71.02

Facioscapulohumeral muscular dystrophy

    2019 - New Code 2020 2021 2022 Billable/Specific Code
Applicable To
  • Scapulohumeral muscular dystrophy
Other specified muscular dystrophies
ICD-10-CM Diagnosis Code G71.09

Other specified muscular dystrophies

    2019 - New Code 2020 2021 2022 Billable/Specific Code
Applicable To
  • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
  • Congenital muscular dystrophy NOS
  • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
  • Distal muscular dystrophy
  • Limb-girdle muscular dystrophy
  • Ocular muscular dystrophy
  • Oculopharyngeal muscular dystrophy
  • Scapuloperoneal muscular dystrophy
Myotonic muscular dystrophy
ICD-10-CM Diagnosis Code G71.11

Myotonic muscular dystrophy

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
  • Dystrophia myotonica [Steinert]
  • Myotonia atrophica
  • Myotonic dystrophy
  • Proximal myotonic myopathy (PROMM)
  • Steinert disease
Myotonia congenita
ICD-10-CM Diagnosis Code G71.12

Myotonia congenita

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
  • Acetazolamide responsive myotonia congenita
  • Dominant myotonia congenita [Thomsen disease]
  • Myotonia levior
  • Recessive myotonia congenita [Becker disease]
Myotonic chondrodystrophy
ICD-10-CM Diagnosis Code G71.13

Myotonic chondrodystrophy

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
  • Chondrodystrophic myotonia
  • Congenital myotonic chondrodystrophy
  • Schwartz-Jampel disease
Drug induced myotonia
ICD-10-CM Diagnosis Code G71.14

Drug induced myotonia

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Use Additional
  • code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
Other specified myotonic disorders
ICD-10-CM Diagnosis Code G71.19

Other specified myotonic disorders

    2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
Applicable To
  • Myotonia fluctuans
  • Myotonia permanens
  • Neuromyotonia [Isaacs]
  • Paramyotonia congenita (of von Eulenburg)
  • Pseudomyotonia
  • Symptomatic myotonia
Congenital myopathy, unspecified
ICD-10-CM Diagnosis Code G71.20

Congenital myopathy, unspecified

    2021 - New Code 2022 Billable/Specific Code