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Results 1 - 10 of 42 for Primary dilated cardiomyopathy
  1. Dilated cardiomyopathy 
    Cardiomyopathy is disease in which the heart muscle becomes weakened, stretched, or has another structural problem. Dilated cardiomyopathy ...
    https://medlineplus.gov/ency/article/000168.htm - Medical Encyclopedia
  2. Familial dilated cardiomyopathy 
    ... FDC Primary familial dilated cardiomyopathy Genetic Testing Registry: Primary dilated cardiomyopathy Cardiomyopathy, dilated, 1a Cardiomyopathy, dilated, 1e Dilated cardiomyopathy ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  3. Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    Cardiomyopathy/Children ... Cardiomyopathy ... Children's Cardiomyopathy Foundation
    https://www.childrenscardiomyopathy.org/pages/about-disease/causes - External Health Links
  4. TNNT2 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  5. TNNI3 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  6. MYH7 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  7. MYBPC3 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  8. LAMP2 gene 
    ... Bonilla E, Nonaka I, DiMauro S, Hirano M. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease). Nature. 2000 Aug 24; ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics
  9. Primary coenzyme Q10 deficiency 
    ... that enlarges and weakens the heart muscle (hypertrophic cardiomyopathy) can also occur in primary coenzyme Q10 deficiency. The prevalence of primary coenzyme ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  10. Primary carnitine deficiency 
    ... fats and produce energy.Signs and symptoms of primary carnitine deficiency typically appear during infancy or early childhood and can include severe brain dysfunction (encephalopathy), a weakened and enlarged heart (cardiomyopathy), vomiting, muscle weakness, and low blood glucose (hypoglycemia). ...
    https://medlineplus.gov/.../condition/primary-carnitine-deficiency - Genetics
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