| ICD-10-CM-2023 > G00-G99 > G70-G73 > G71 |
G70-G73 | Diseases of myoneural junction and muscle | |
G71 | Primary disorders of muscles | |
Excl2.: | arthrogryposis multiplex congenita (Q74.3) metabolic disorders (E70-E88) myositis (M60.-) | |
G71.0 | Muscular dystrophy | |
G71.00 | Muscular dystrophy, unspecified | |
G71.01 | Duchenne or Becker muscular dystrophy | |
Info: | Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy Benign [Becker] muscular dystrophy Severe [Duchenne] muscular dystrophy | |
G71.02 | Facioscapulohumeral muscular dystrophy | |
Info: | Scapulohumeral muscular dystrophy | |
G71.03 | Limb girdle muscular dystrophies | |
G71.031 | Autosomal dominant limb girdle muscular dystrophy | |
Info: | LGMD D4 calpain-3-related LGMD D5 collagen 6-related Limb girdle muscular dystrophy type 1 | |
G71.032 | Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction | |
Info: | Limb girdle muscular dystrophy type 2A LGMD R1 calpain-3-related Primary calpainopathy | |
G71.033 | Limb girdle muscular dystrophy due to dysferlin dysfunction | |
Info: | Dysferlinopathy LGMD R2 dysferlin-related Limb girdle muscular dystrophy type 2B Miyoshi Myopathy type 1 | |
G71.034 | Limb girdle muscular dystrophy due to sarcoglycan dysfunction | |
G71.0340 | Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified | |
Info: | Sarcoglycanopathy, NOS | |
G71.0341 | Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction | |
Info: | Alpha sarcoglycanopathy Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency Limb girdle muscular dystrophy type 2D | |
G71.0342 | Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction | |
Info: | Beta sarcoglycanopathy Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency Limb girdle muscular dystrophy type 2E | |
G71.0349 | Limb girdle muscular dystrophy due to other sarcoglycan dysfunction | |
Info: | 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 | |
G71.035 | Limb girdle muscular dystrophy due to anoctamin-5 dysfunction | |
Info: | Anoctamin-5-related LGMD R12 Anoctaminopathy Autosomal recessive limb girdle muscular dystrophy type 2L Miyoshi myopathy type 3 | |
G71.038 | Other limb girdle muscular dystrophy | |
Info: | 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 | |
G71.039 | Limb girdle muscular dystrophy, unspecified | |
G71.09 | Other specified muscular dystrophies | |
Info: | 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 | |
G71.1 | Myotonic disorders | |
G71.11 | Myotonic muscular dystrophy | |
Info: | Dystrophia myotonica [Steinert] Myotonia atrophica Myotonic dystrophy Proximal myotonic myopathy (PROMM) Steinert disease | |
G71.12 | Myotonia congenita | |
Info: | Acetazolamide responsive myotonia congenita Dominant myotonia congenita [Thomsen disease] Myotonia levior Recessive myotonia congenita [Becker disease] | |
G71.13 | Myotonic chondrodystrophy | |
Info: | Chondrodystrophic myotonia Congenital myotonic chondrodystrophy Schwartz-Jampel disease | |
G71.14 | Drug induced myotonia | |
Use add'l | code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5) | |
G71.19 | Other specified myotonic disorders | |
Info: | Myotonia fluctuans Myotonia permanens Neuromyotonia [Isaacs] Paramyotonia congenita (of von Eulenburg) Pseudomyotonia Symptomatic myotonia | |
G71.2 | Congenital myopathies | |
Excl2.: | arthrogryposis multiplex congenita (Q74.3) | |
G71.20 | Congenital myopathy, unspecified | |
G71.21 | Nemaline myopathy | |
G71.22 | Centronuclear myopathy | |
G71.220 | X-linked myotubular myopathy | |
Info: | Myotubular (centronuclear) myopathy | |
G71.228 | Other centronuclear myopathy | |
Info: | Autosomal centronuclear myopathy Autosomal dominant centronuclear myopathy Autosomal recessive centronuclear myopathy Centronuclear myopathy, NOS | |
G71.29 | Other congenital myopathy | |
Info: | Central core disease Minicore disease Multicore disease Multiminicore disease | |
G71.3 | Mitochondrial myopathy, not elsewhere classified | |
Excl1.: | 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) | |
G71.8 | Other primary disorders of muscles | |
G71.9 | Primary disorder of muscle, unspecified | |
Info: | Hereditary myopathy NOS | |
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