Cardiomyopathy

Synonyms
Myocardiopathy
Subtypes
Restrictive cardiomyopathy
May Cause
Acyanotic congenital heart disease with normal pulmonary vascularity
Calcification in great vessels
Calcification in heart
Cardiomegaly
Cardiomegaly in childhood
Enlarged pulmonary veins
Generalized pulmonary arterial hypovascularity
Heart failure
Heart failure in childhood
Heart failure in the first month of life
Heart failure in the first week of life
Hydrops fetalis
Left atrial enlargement
Left ventricular enlargement
Massive cardiomegaly
Mitochondrial disorder
Mitral insufficiency
Pleural effusion with enlarged heart
Pulmonary venous hypertension
Small aortic arch
Small ascending aorta
Third mogul sign
May Be Caused by
 Common
AIDS
Amyloidosis
Anemia
Aortic stenosis
Chagas disease
Coarctation of aorta
Coxsackie virus
Dermatomyositis
Diphtheria
Endocardial fibroelastosis
Gaucher disease
Hemochromatosis
Hunter syndrome
Hurler syndrome
Hypertension
Hyperthyroidism
Idiopathic dilated cardiomyopathy
Idiopathic hypertrophic subaortic stenosis
Infant of diabetic mother
Infantile hypothyroidism
Infectious myocarditis
Mucolipidosis type 2
Myocardial ischemia
Niemann-Pick disease
Noonan syndrome
Nutritional deficiency
Rheumatic fever
Rheumatoid arthritis
Rubella
Scleroderma
Sepsis
Systemic lupus erythematosus
Thyrotoxicosis
Toxoplasmosis
Tuberous sclerosis
 Uncommon
3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency
Acromegaly
Adriamycin
Anomalous left coronary artery from pulmonary artery
Aspartylglycosaminuria
Bardet-Biedl syndrome
Barth syndrome
Becker muscular dystrophy
Beriberi
Cardiac fibroma
Cardiac rhabdomyoma
Cardiomyopathy - cataract - hip spine disease
Cardiomyopathy - hypotonia - lactic acidosis
Cardiomyopathy - renal anomalies
Carnitine deficiency syndrome
Chronic magnesium deficiency
Clark-Howel-Evans-McConnell syndrome
Cobalt cardiomyopathy
Cocaine abuse
Congenital adrenal hyperplasia
Coronary artery calcification
Cushing syndrome
Degos syndrome
Diabetes mellitus
Doxorubicin
Duchenne muscular dystrophy
Emery-Dreifuss muscular dystrophy
Endomyocardial fibrosis
Eosinophilia-myalgia syndrome
Fabry disease
Facioscapulohumeral muscular dystrophy
Familial cardiomyopathy
Familial hypermethioninemia
Farber disease
Fetal rubella syndrome
Friedreich ataxia
Fucosidosis type 1
Geleophysic dysplasia
Glycogen storage disease type 2
Glycogen storage disease type 3
GM1 gangliosidosis
Heart-hand syndrome
Heart-hand syndrome type 3
HELLP syndrome
Hemolytic-uremic syndrome
Hyperphosphatasemia
Hypertrichotic osteochondrodysplasia
Hypothyroidism
Kearns-Sayre syndrome
Keshan disease
King syndrome
Kugelberg-Welander syndrome
Leigh disease
LEOPARD syndrome
Leukemia
Limb-girdle muscular dystrophy
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Lymphoma
Malonic aciduria and malonyl CoA decarboxylase deficiency
Mannosidosis type 1
Marles-Chudley syndrome
Metastatic disease to heart
Microcephaly - cardiomyopathy
Microphthalmia - linear skin defects syndrome
Mitochondrial disease
Mitochondrial myopathy-cardiomyopathy-cataract-lactic acidosis
Mucolipidosis type 3
Mucopolysaccharidosis
Myotubular myopathy
Myxedema
Najjar syndrome
Nemaline myopathy
Neuroacanthocytosis
Palmoplantar keratosis
Polymyositis-dermatomyositis
Polyneuropathy of Roussy-Lévy
Postpartum state
Potassium depletion
Pseudoxanthoma elasticum
Radiation therapy
Refsum syndrome
Rippling muscle disease
Sarcoidosis
Spondylometaphyseal dysplasia Sedaghatian type
Subvalvular left ventricular aneurysm
Takotsubo-shaped cardiomyopathy
Toriello-Carey syndrome
Tubular renal disease - cardiomyopathy
Uremia
Uruguay facio-cardio-musculo-skeletal syndrome
Vici syndrome
Vitamin B deficiency
Werdnig-Hoffmann disease
Werner syndrome
Yunis-Varon syndrome

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