This page needs to be proofread.
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
- G71.11 Myotonic muscular dystrophy
- 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.
