ICD 10 Range Diseases of myoneural junction and muscle

• 1 Myasthenia gravis and other myoneural disorders( G70 )

• 2 Myasthenia gravis( G70.0 )

• 3 Myasthenia gravis without (acute) exacerbation( G70.00 )

• 4 Myasthenia gravis with (acute) exacerbation( G70.01 )

• 5 Toxic myoneural disorders( G70.1 )

• 6 Congenital and developmental myasthenia( G70.2 )

• 7 Other specified myoneural disorders( G70.8 )

• 8 Lambert-Eaton syndrome, unspecified( G70.80 )

• 9 Lambert-Eaton syndrome in disease classified elsewhere( G70.81 )

• 10 Other specified myoneural disorders( G70.89 )

• 11 Myoneural disorder, unspecified( G70.9 )

• 12 Primary disorders of muscles( G71 )

• 13 Muscular dystrophy( G71.0 )

• 14 Muscular dystrophy, unspecified( G71.00 )

• 15 Duchenne or Becker muscular dystrophy( G71.01 )

• 16 Facioscapulohumeral muscular dystrophy( G71.02 )

• 17 Limb girdle muscular dystrophies( G71.03 )

• 18 Autosomal dominant limb girdle muscular dystrophy( G71.031 )

• 19 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction( G71.032 )

• 20 Limb girdle muscular dystrophy due to dysferlin dysfunction( G71.033 )

• 21 Limb girdle muscular dystrophy due to sarcoglycan dysfunction( G71.034 )

• 22 Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified( G71.0340 )

• 23 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction( G71.0341 )

• 24 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction( G71.0342 )

• 25 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction( G71.0349 )

• 26 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction( G71.035 )

• 27 Other limb girdle muscular dystrophy( G71.038 )

• 28 Limb girdle muscular dystrophy, unspecified( G71.039 )

• 29 Other specified muscular dystrophies( G71.09 )

• 30 Myotonic disorders( G71.1 )

• 31 Myotonic muscular dystrophy( G71.11 )

• 32 Myotonia congenita( G71.12 )

• 33 Myotonic chondrodystrophy( G71.13 )

• 34 Drug induced myotonia( G71.14 )

• 35 Other specified myotonic disorders( G71.19 )

• 36 Congenital myopathies( G71.2 )

• 37 Congenital myopathy, unspecified( G71.20 )

• 38 Nemaline myopathy( G71.21 )

• 39 Centronuclear myopathy( G71.22 )

• 40 X-linked myotubular myopathy( G71.220 )

• 41 Other centronuclear myopathy( G71.228 )

• 42 Other congenital myopathy( G71.29 )

• 43 Mitochondrial myopathy, not elsewhere classified( G71.3 )

• 44 Other primary disorders of muscles( G71.8 )

• 45 Primary disorder of muscle, unspecified( G71.9 )

• 46 Other and unspecified myopathies( G72 )

• 47 Drug-induced myopathy( G72.0 )

• 48 Alcoholic myopathy( G72.1 )

• 49 Myopathy due to other toxic agents( G72.2 )

• 50 Periodic paralysis( G72.3 )

• 51 Inflammatory and immune myopathies, not elsewhere classified( G72.4 )

• 52 Inclusion body myositis [IBM]( G72.41 )

• 53 Other inflammatory and immune myopathies, not elsewhere classified( G72.49 )

• 54 Other specified myopathies( G72.8 )

• 55 Critical illness myopathy( G72.81 )

• 56 Other specified myopathies( G72.89 )

• 57 Myopathy, unspecified( G72.9 )

• 58 Disorders of myoneural junction and muscle in diseases classified elsewhere( G73 )

• 59 Lambert-Eaton syndrome in neoplastic disease( G73.1 )

• 60 Myasthenic syndromes in other diseases classified elsewhere( G73.3 )

• 61 Myopathy in diseases classified elsewhere( G73.7 )