Genetic | Genetic hypertrophic cardiomyopathy*¶ | Genetic dilated cardiomyopathyΔ | Metabolic | Endocrine | Acromegaly*¶Δ | ThyrotoxicosisΔ | Hypothyroidism*¶Δ | Pheochromocytoma*¶Δ | Diabetes melllitus | Familial storage diseases | Glycogen storage diseases*Δ | Refsum disease | Niemann-Pick disease | Hand-Schuller-Christian disease | Fabry's disease*Δ | Gangliosiderosis | Gaucher's disease¶Δ | Sandhoff's diseaseΔ | MucopolysaccharidosisΔ | Hunter's syndrome | Hurler's syndrome | Nutritional | BeriberiΔ | KwashiokorΔ | Pellagra | Selenium deficiency | (Keshan's disease)Δ | Other | HypokalemiaΔ | Carnitine deficiencyΔ | UremiaΔ | | Hematologic/oncologic | Hematologic disorders | LeukemiaΔ | Myeloma | Sickle cell anemiaΔ | AnemiaΔ | Henoch-Schonlein purpuraΔ | Neoplastic diseases | Primary neoplasms¶ | Metastatic neoplasms¶ | Deposits | Hemochromatosis¶Δ | Oxalosis | Ochronosis | Amyloid disease¶ | Heredofamilial neurologic and neuromuscular diseases | Progressive muscular dystrophy (Duchenne)Δ | Limb-girdle muscular dystrophy (Erb)Δ | Fascioscapulohumeral dystrophy (Landouzy-Dejerine) | Humeroperoneal ataxia | Friedreich's ataxia* | Myotonia atrophica (Steinert)Δ | Myasthenia gravis | Chronic progressive external opthmoplegia (Kearns-Savre) | Familial centronuclear myopathy | Juvenile progressive spinal muscular atrophy (Kugelberg-Welander) | Neurofibromatosis* | | Endomyocardial diseases | Endomyocardial fibrosis¶Δ | Hypereosiinophilic heart disease | (Loffler's)¶ | Endocardial fibroelastosis¶Δ | Inflammatory | Connective tissue diseases | Rheumatoid heart diseaseΔ | Ankylosing spondylitis | Systemic lupus erythematosusΔ | Scleroderma¶Δ | DermatomyositisΔ | Periarteritis nodosa | Granulomatous | SarcoidΔ | Wegener's granulomatosisΔ | Granulomatous myocarditisΔ | Other inflammation | Giant cell myocarditisΔ | Hypersensitivity myocarditisΔ | |