G71.22 Centronuclear myopathy

Non-billable header with 2 child codes.

Applies from G71 Primary disorders of muscles

Excludes2 (not included here)

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

Applies from G71.2 Congenital myopathies

Excludes2 (not included here)

• arthrogryposis multiplex congenita (Q74.3)

Codes under G71.22

• G71.220 X-linked myotubular myopathy
• G71.228 Other centronuclear myopathy

Code annotations containing back-references to G71.22

Back-references to G71

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

Nearby codes

• G71.14 Drug induced myotonia
• G71.19 Other specified myotonic disorders
• G71.2 Congenital myopathies
• G71.20 Congenital myopathy, unspecified
• G71.21 Nemaline myopathy
• G71.22 Centronuclear myopathy (this code)
• G71.220 X-linked myotubular myopathy
• G71.228 Other centronuclear myopathy
• G71.29 Other congenital myopathy
• G71.3 Mitochondrial myopathy, not elsewhere classified
• G71.8 Other primary disorders of muscles