Etiologic classification of cardiomyopathy-II

• Genetic hypertrophic cardiomyopathy*^¶
• Genetic dilated cardiomyopathy^Δ

• Leukemia^Δ
• Myeloma
• Sickle cell anemia^Δ
• Anemia^Δ
• Henoch-Schonlein purpura^Δ

Neoplastic diseases

• Primary neoplasms^¶
• Metastatic neoplasms^¶

• Endomyocardial fibrosis^¶Δ
• Hypereosiinophilic heart disease (Loffler)^¶
• Endocardial fibroelastosis^¶Δ

• Acromegaly*^¶Δ
• Thyrotoxicosis^Δ
• Hypothyroidism*^¶Δ
• Pheochromocytoma*^¶Δ
• Diabetes melllitus

Familial storage diseases

• Glycogen storage diseases*^Δ
• Refsum disease
• Niemann-Pick disease
• Hand-Schuller-Christian disease
• Fabry disease*^Δ
• Gangliosiderosis
• Gaucher disease^¶Δ
• Sandhoff disease^Δ
• Mucopolysaccharidosis^Δ
• Hunter syndrome
• Hurler syndrome

Nutritional

• Beriberi^Δ
• Kwashiokor^Δ
• Pellagra
• Selenium deficiency (Keshan disease)^Δ

Other

• Hypokalemia^Δ
• Carnitine deficiency^Δ
• Uremia^Δ

• Hemochromatosis^¶Δ
• Oxalosis
• Ochronosis
• Amyloid disease^¶

• Rheumatoid heart disease^Δ
• Ankylosing spondylitis
• Systemic lupus erythematosus^Δ
• Scleroderma^¶Δ
• Dermatomyositis^Δ
• Periarteritis nodosa

Granulomatous

• Sarcoid^Δ
• Wegener granulomatosis^Δ
• Granulomatous myocarditis^Δ

Other inflammation

• Giant cell myocarditis^Δ
• Hypersensitivity myocarditis^Δ

• Progressive muscular dystrophy (Duchenne)^Δ
• Limb-girdle muscular dystrophy (Erb)^Δ
• Fascioscapulohumeral dystrophy (Landouzy-Dejerine)
• Humeroperoneal ataxia
• Friedreich ataxia*
• Myotonia atrophica (Steinert)^Δ
• Myasthenia gravis
• Chronic progressive external opthmoplegia (Kearns-Savre)
• Familial centronuclear myopathy
• Juvenile progressive spinal muscular atrophy (Kugelberg-Welander)
• Neurofibromatosis*