- G71.01 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 G71.01 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G71.01 – other international versions of ICD-10 G71.01 may differ.
ICD-10-CM G71.01 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
- Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
- Benign [Becker] muscular dystrophy
- Severe [Duchenne] muscular dystrophy
Code History
- 2019 (effective 10/1/2018): New code
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to G71.01:
- dystrophy > Becker\’s
- Duchenne-Griesinger > Disease, diseased
- Duchenne\’s > Disease, diseased
- muscular dystrophy > Duchenne\’s G71.01
- pseudohypertrophy, muscles > Duchenne\’s G71.01
- muscular dystrophy > disease or syndrome G12.22
- muscular dystrophy > due to or associated with G12.22
- autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker > Dystrophy, dystrophia
- Becker\’s type > Dystrophy, dystrophia
- Duchenne\’s type > Dystrophy, dystrophia
- Gower\’s muscular > Dystrophy, dystrophia
- autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker > muscular G71.00
- benign (Becker type) > muscular G71.00
- Duchenne type > muscular G71.00
- Gower\’s > muscular G71.00
- pseudohypertrophic (infantile) > muscular G71.00
- severe (Duchenne type) > muscular G71.00
- muscular dystrophy > Gower\’s
- muscular dystrophy > due to or associated with G12.22