- G71.02 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 G71.02 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G71.02 – other international versions of ICD-10 G71.02 may differ.
ICD-10-CM G71.02 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
- Scapulohumeral 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 G71.02:
- fascioscapulohumeral (Landouzy- Déjérine) > Atrophy, atrophic (of)
- Landouzy-Déjérine > Atrophy, atrophic (of)
- pseudohypertrophic > muscle, muscular (diffuse) (general) (idiopathic) (primary) M62.50
- pseudohypertrophic (muscle) > Atrophy, atrophic (of)
- Erb (-Landouzy) > Disease, diseased
- Erb\’s > Dystrophy, dystrophia
- Landouzy-Déjérine > Dystrophy, dystrophia
- Erb type > muscular G71.00
- facioscapulohumeral > muscular G71.00
- Landouzy-Déjérine type > muscular G71.00
- scapulohumeral > muscular G71.00
- disease > Erb\’s
- pseudohypertrophic muscular dystrophy > Erb\’s
- facioscapulohumeral > Myopathy G72.9
- scapulohumeral > Myopathy G72.9
- pseudohypertrophic > muscle, muscular NEC G72.89