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Results 21 - 30 of 112 for Idiopathic cardiomyopathy
  1. DES gene 
    ... more likely to have a weakened heart muscle (cardiomyopathy) than people with myofibrillar myopathy caused by mutations in other genes. In some cases, cardiomyopathy is the first symptom of this condition. More ...
    https://medlineplus.gov/genetics/gene/des - Genetics
  2. TNNT2 gene 
    ... in the TNNT2 gene can cause familial hypertrophic cardiomyopathy, a condition characterized by thickening (hypertrophy) of the ... with this condition. Although some people with hypertrophic cardiomyopathy have no obvious health effects, all affected individuals ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  3. MYBPC3 gene 
    ... gene are a common cause of familial hypertrophic cardiomyopathy, accounting for up to 30 percent of all ... cardiac muscle. Although some people with familial hypertrophic cardiomyopathy have no obvious health effects, all affected individuals ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  4. DSC2 gene 
    ... form of heart disease called arrhythmogenic right ventricular cardiomyopathy (ARVC).The known mutation, which is written as ... that abnormal cell signaling may also contribute to cardiomyopathy in people with this condition.Several other mutations ...
    https://medlineplus.gov/genetics/gene/dsc2 - Genetics
  5. SGCD gene 
    ... 2F have developed a heart condition called dilated cardiomyopathy. Dilated cardiomyopathy is a form of heart disease that enlarges ... muscle, preventing it from pumping blood efficiently. Dilated cardiomyopathy progresses rapidly and can be life-threatening.Forms ...
    https://medlineplus.gov/genetics/gene/sgcd - Genetics
  6. LAMP2 gene 
    ... condition characterized by weakening of the heart muscle (cardiomyopathy), weakening of skeletal muscles (myopathy), and intellectual disabilities. ... Some people with LAMP2 gene variants develop hypertrophic cardiomyopathy without the other characteristic features of Danon disease. ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics
  7. PKP2 gene 
    ... been identified in people with arrhythmogenic right ventricular cardiomyopathy (ARVC). This condition most commonly affects the myocardium ... DP. Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2. Circulation. 2006 ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  8. PRKAG2 gene 
    ... with these mutations also have features of hypertrophic cardiomyopathy, a form of heart disease that enlarges and ... enlarges these cells, which may lead to hypertrophic cardiomyopathy. Researchers continue to investigate whether an abnormal buildup ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  9. Duchenne and Becker muscular dystrophy 
    ... dystrophy are associated with a heart condition called cardiomyopathy. This form of heart disease weakens the cardiac ... efficiently. In both Duchenne and Becker muscular dystrophy, cardiomyopathy typically begins in adolescence. Later, the heart muscle ...
    https://medlineplus.gov/.../duchenne-and-becker-muscular-dystrophy - Genetics
  10. LDB3 gene 
    ... Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/ldb3 - Genetics
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