ICD-10 CM Code G71.2
G71.2
Congenital myopathies
Inclusion Term
- Central core disease
- Fiber-type disproportion
- Minicore disease
- Multicore disease
- Myotubular (centronuclear) myopathy
- Nemaline myopathy
Excludes Type 1
- arthrogryposis multiplex congenita (Q74.3)
Excludes Type 2
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
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