G71.02 Facioscapulohumeral muscular dystrophy

Billable ICD-10-CM code, FY2026.

Applicable to

• Scapulohumeral muscular dystrophy

Applies from G71 Primary disorders of muscles

Excludes2 (not included here)

• arthrogryposis multiplex congenita (Q74.3)
• metabolic disorders (E70-E88)
• myositis (M60.-)

Risk adjustment (HCC)

• CMS-HCC V28: HCC 197 — Muscular Dystrophy
• CMS-HCC V22: HCC 76 — Muscular Dystrophy
• ESRD V24: HCC 76

MS-DRG index

Defines the logic of DRG(s) 091-093 in MDC 01.

Code annotations containing back-references to G71.02

Back-references to G71.0

• Code First: Z99.3 Dependence on wheelchair ("muscular dystrophy (G71.0-)")

Back-references to G71

• Code First: M62.84 Sarcopenia ("primary disorders of muscles (G71.-)")

Diagnosis Index entries for G71.02

• Atrophy, atrophic (of) › fascioscapulohumeral (Landouzy- Déjérine)
• Atrophy, atrophic (of) › Landouzy-Déjérine
• Atrophy, atrophic (of) › muscle, muscular (diffuse) (general) (idiopathic) (primary) › pseudohypertrophic
• Atrophy, atrophic (of) › pseudohypertrophic (muscle)
• Disease, diseased › Erb (-Landouzy)
• Dystrophy, dystrophia › Erb's
• Dystrophy, dystrophia › Landouzy-Déjérine
• Dystrophy, dystrophia › muscular › Erb type
• Dystrophy, dystrophia › muscular › facioscapulohumeral
• Dystrophy, dystrophia › muscular › Landouzy-Déjérine type
• Dystrophy, dystrophia › muscular › scapulohumeral
• Erb's › disease
• Erb's › pseudohypertrophic muscular dystrophy
• Fascioscapulohumeral myopathy
• Landouzy-Déjérine dystrophy or facioscapulohumeral atrophy
• Myopathy › facioscapulohumeral
• Myopathy › scapulohumeral
• Paralysis, paralytic (complete) (incomplete) › muscle, muscular NEC › pseudohypertrophic
• Pseudohypertrophic muscular dystrophy (Erb's)
• Scapulohumeral myopathy

Nearby codes

• 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 (this code)
• 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