- G71.09 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 G71.09 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G71.09 – other international versions of ICD-10 G71.09 may differ.
ICD-10-CM G71.09 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
- 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
- Ocular muscular dystrophy
- Oculopharyngeal muscular dystrophy
- Scapuloperoneal 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 G71.09:
- progressive muscular dystrophy > due to I42.6
- scapuloperoneal with early contractures [Emery-Dreifuss] > benign (Becker type) G71.01
- congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber) > muscular G71.00
- distal > muscular G71.00
- Emery-Dreifuss > muscular G71.00
- hereditary (progressive) > muscular G71.00
- progressive (hereditary) > muscular G71.00
- scapuloperoneal > muscular G71.00
- specified type NEC > muscular G71.00
- ocular > Dystrophy, dystrophia
- oculopharyngeal > Dystrophy, dystrophia
- scapuloperoneal > Dystrophy, dystrophia
- pseudomuscular > Hypertrophy, hypertrophic
- progressive muscular dystrophy > in (due to) E51.12
- distal > Myopathy G72.9
- ocular > Myopathy G72.9
- oculopharyngeal > Myopathy G72.9
- pseudohypertrophic (muscle) > Paralysis, paralytic (complete) (incomplete) G83.9
- pseudohypertrophic > Paresis
- scapuloperoneal > Syndrome