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2009 ICD-9-CM
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359 Muscular dystrophies and other myopathies
Excludes: idiopathic polymyositis (710.4) | |
 eicd10 | 359.0 Congenital hereditary muscular dystrophy
Benign congenital myopathy
Central core disease
Centronuclear myopathy
Myotubular myopathy
Nemaline body disease
Excludes: arthrogryposis multiplex congenita (754.89) |
| eicd10 | 359.1 Hereditary progressive muscular dystrophy
Muscular dystrophy:
NOS
distal
Duchenne
Erb's
fascioscapulohumeral
Gower's
Landouzy-Déjérine
limb-girdle
ocular
oculopharyngeal |
 | |
| eicd10 | 359.3 Periodic paralysis
Familial periodic paralysis
Hyperkalemic periodic paralysis
Hypokalemic familial periodic paralysis
Hypokalemic periodic paralysis
Potassium sensitive periodic paralysis
Excludes: paramyotonia congenita (of von Eulenburg) (359.29) |
| eicd10 | 359.4 Toxic myopathy
Use additional E code to identify toxic agent |
| eicd10 | 359.5 Myopathy in endocrine diseases classified elsewhere
Code first underlying disease, as:
Addison's disease (255.41)
Cushing's syndrome (255.0)
hypopituitarism (253.2)
myxedema (244.0-244.9)
thyrotoxicosis (242.0-242.9) |
| eicd10 | 359.6 Symptomatic inflammatory myopathy in diseases classified elsewhere
Code first underlying disease, as:
amyloidosis (277.30-277.39)
disseminated lupus erythematosus (710.0)
malignant neoplasm (140.0-208.9)
polyarteritis nodosa (446.0)
rheumatoid arthritis (714.0)
sarcoidosis (135)
scleroderma (710.1)
Sjögren's disease (710.2) |
| |
| eicd10 | 359.9 Myopathy, unspecified |