 G71 |
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Primary disorders of muscles  |
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| Excludes2 |
arthrogryposis multiplex congenita (Q74.3)
metabolic disorders (E70-E88)
myositis (M60.-)
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| G71.0 |
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Muscular dystrophy |
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 G71.00 |
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Muscular dystrophy, unspecified |
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| G71.01 |
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Duchenne or Becker muscular dystrophy |
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| Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy | | Benign [Becker] muscular dystrophy | | Severe [Duchenne] muscular dystrophy |
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| G71.02 |
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Facioscapulohumeral muscular dystrophy |
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| Scapulohumeral muscular dystrophy |
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| G71.03 |
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Limb girdle muscular dystrophies |
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| G71.031 |
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Autosomal dominant limb girdle muscular dystrophy |
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| LGMD D4 calpain-3-related | | LGMD D5 collagen 6-related | | Limb girdle muscular dystrophy type 1 |
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| G71.032 |
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Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction |
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| Limb girdle muscular dystrophy type 2A | | LGMD R1 calpain-3-related | | Primary calpainopathy |
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| G71.033 |
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Limb girdle muscular dystrophy due to dysferlin dysfunction |
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| Dysferlinopathy | | LGMD R2 dysferlin-related | | Limb girdle muscular dystrophy type 2B | | Miyoshi Myopathy type 1 |
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| G71.034 |
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Limb girdle muscular dystrophy due to sarcoglycan dysfunction |
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| G71.0340 |
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Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified |
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| G71.0341 |
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Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction |
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| Alpha sarcoglycanopathy | | Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency | | Limb girdle muscular dystrophy type 2D |
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| G71.0342 |
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Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction |
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| Beta sarcoglycanopathy | | Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency | | Limb girdle muscular dystrophy type 2E |
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| G71.0349 |
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Limb girdle muscular dystrophy due to other sarcoglycan dysfunction |
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| Delta sarcoglycanopathy | | Delta-sarcoglycan-related LGMD R6 | | Gamma sarcoglycanopathy | | Gamma-sarcoglycan-related LGMD R5 | | Limb girdle muscular dystrophy type 2C | | Limb girdle muscular dystrophy type 2F |
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| G71.035 |
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Limb girdle muscular dystrophy due to anoctamin-5 dysfunction |
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| Anoctamin-5-related LGMD R12 | | Anoctaminopathy | | Autosomal recessive limb girdle muscular dystrophy type 2L | | Miyoshi myopathy type 3 |
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| G71.038 |
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Other limb girdle muscular dystrophy |
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| LGMD R9 FKRP-related | | LGMD R22 collagen 6-related | | Limb girdle muscular dystrophy due to fukutin related protein dysfunction | | Limb girdle muscular dystrophy type 2I | | Other autosomal recessive limb girdle muscular dystrophy |
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| G71.039 |
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Limb girdle muscular dystrophy, unspecified |
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| G71.09 |
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Other specified muscular dystrophies |
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| Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss] | | Congenital muscular dystrophy NOS | | Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber | | Distal muscular dystrophy | | Ocular muscular dystrophy | | Oculopharyngeal muscular dystrophy | | Scapuloperoneal muscular dystrophy |
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| G71.1 |
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Myotonic disorders |
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| G71.11 |
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Myotonic muscular dystrophy |
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| Dystrophia myotonica [Steinert] | | Myotonia atrophica | | Myotonic dystrophy | | Proximal myotonic myopathy (PROMM) | | Steinert disease |
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| G71.12 |
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Myotonia congenita |
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| Acetazolamide responsive myotonia congenita | | Dominant myotonia congenita [Thomsen disease] | | Myotonia levior | | Recessive myotonia congenita [Becker disease] |
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| G71.13 |
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Myotonic chondrodystrophy |
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| Chondrodystrophic myotonia | | Congenital myotonic chondrodystrophy | | Schwartz-Jampel disease |
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| G71.14 |
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Drug induced myotonia |
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| UseAdditionalCode |
code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
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| G71.19 |
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Other specified myotonic disorders |
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| Myotonia fluctuans | | Myotonia permanens | | Neuromyotonia [Isaacs] | | Paramyotonia congenita (of von Eulenburg) | | Pseudomyotonia | | Symptomatic myotonia |
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| G71.2 |
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Congenital myopathies |
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| Excludes2 |
arthrogryposis multiplex congenita (Q74.3)
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| G71.20 |
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Congenital myopathy, unspecified |
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| G71.21 |
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Nemaline myopathy |
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| G71.22 |
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Centronuclear myopathy |
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| G71.220 |
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X-linked myotubular myopathy |
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| Myotubular (centronuclear) myopathy |
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| G71.228 |
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Other centronuclear myopathy |
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| Autosomal centronuclear myopathy | | Autosomal dominant centronuclear myopathy | | Autosomal recessive centronuclear myopathy | | Centronuclear myopathy, NOS |
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| G71.29 |
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Other congenital myopathy |
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| Central core disease | | Minicore disease | | Multicore disease | | Multiminicore disease |
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| G71.3 |
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Mitochondrial myopathy, not elsewhere classified |
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| Excludes1 |
Kearns-Sayre syndrome (H49.81)
Leber's disease (H47.21)
Leigh's encephalopathy (G31.82)
mitochondrial metabolism disorders (E88.4.-)
Reye's syndrome (G93.7)
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| G71.8 |
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Other primary disorders of muscles |
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| G71.9 |
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Primary disorder of muscle, unspecified |
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