G71.03 Limb girdle muscular dystrophies

Non-billable header with 8 child codes.

Applies from G71 Primary disorders of muscles

Excludes2 (not included here)

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

Codes under G71.03

• 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
• G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
• G71.036 Limb girdle muscular dystrophy due to fukutin related protein dysfunction
• G71.038 Other limb girdle muscular dystrophy
• G71.039 Limb girdle muscular dystrophy, unspecified

Code annotations containing back-references to G71.03

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.-)")

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
• G71.03 Limb girdle muscular dystrophies (this code)
• 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
• G71.0340 Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified