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 muscular dystrophy
 * Facioscapulohumeral muscular dystrophy
 * Limb-girdle muscular dystrophy
 * Ocular muscular dystrophy
 * Oculopharyngeal muscular dystrophy
 * Scapuloperoneal muscular dystrophy
 * Severe [Duchenne] muscular dystrophy
 * Excludes1: congenital muscular dystrophy NOS (G71.2)
 * congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber (G71.2)
 * G71.1 Myotonic disorders
 * G71.11 Myotonic muscular dystrophy
 * Dystrophia myotonica [Steinert]
 * Myotonia atrophica
 * Myotonic dystrophy
 * Proximal myotonic myopathy (PROMM)
 * Steinert disease
 * G71.12 Myotonia congenita
 * Acetazolamide responsive myotonia congenita
 * Dominant myotonia congenita [Thomsen disease]
 * Myotonia levior
 * Recessive myotonia congenita [Becker disease]
 * G71.13 Myotonic chondrodystrophy
 * Chondrodystrophic myotonia
 * Congenital myotonic chondrodystrophy
 * Schwartz-Jampel disease
 * G71.14 Drug induced myotonia
 * Code first (T36-T50) to identify drug
 * G71.19 Other specified myotonic disorders
 * Myotonia fluctuans
 * Myotonia permanens
 * Neuromyotonia [Isaacs]
 * Paramyotonia congenita (of von Eulenburg)
 * Pseudomyotonia
 * Symptomatic myotonia
 * G71.2 Congenital myopathies
 * Central core disease
 * Congenital muscular dystrophy NOS
 * Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
 * Fiber-type disproportion
 * Minicore disease
 * Multicore disease
 * Myotubular (centronuclear) myopathy
 * Nemaline myopathy
 * Excludes1: arthrogryposis multiplex congenita (Q74.3)
 * G71.