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Results 1 - 10 of 112 for Idiopathic cardiomyopathy
  1. Familial dilated cardiomyopathy is a genetic form of heart disease. It occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of ...
  2. Hypertrophic cardiomyopathy is a heart condition characterized by thickening (hypertrophy) of the heart (cardiac) muscle. When multiple members of a family have the ...
  3. X-linked dilated cardiomyopathy is a form of heart disease. Dilated cardiomyopathy enlarges and weakens the heart (cardiac) muscle, preventing the heart ...
  4. Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a form of heart disease that usually appears in adulthood. ARVC is a disorder of the myocardium, which is the ...
  5. Familial restrictive cardiomyopathy is a genetic form of heart disease. For the heart to beat normally, the heart (cardiac) muscle must ... heart (the ventricles).In people with familial restrictive cardiomyopathy, the heart muscle is stiff and cannot fully ...
  6. Early-onset myopathy with fatal cardiomyopathy (EOMFC) is an inherited muscle disease that affects the skeletal muscles, which are used for movement, and the ...
  7. Dilated cardiomyopathy with ataxia (DCMA) syndrome is an inherited condition characterized by heart problems, movement difficulties, and other features affecting ...
  8. ... condition characterized by weakening of the heart muscle (cardiomyopathy); weakening of the muscles used for movement, called ... and typically survive into mid-adulthood without treatment.Cardiomyopathy is the most common symptom of Danon disease, ...
  9. ... myocardium Left ventricular hypertrabeculation Left ventricular myocardial noncompaction cardiomyopathy Left ventricular non-compaction LVHT LVNC Non-compaction ...
  10. ... Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition Mutations in the ... cause two diseases of the cardiac muscle, dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM). DCM weakens and ...
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