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Results 1 - 10 of 65 for Familial restrictive cardiomyopathy
  1. Familial dilated cardiomyopathy 
    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 ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  2. Familial restrictive cardiomyopathy 
    ... S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  3. Familial hypertrophic cardiomyopathy 
    ... family have the condition, it is known as familial hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy also occurs in people with no ... these cases are considered nonfamilial hypertrophic cardiomyopathy. In familial ... cardiac thickening usually occurs in the interventricular septum, ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  4. TNNI3 gene 
    ... do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ... S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  5. MYH7 gene 
    ... do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ... on PubMed Rodriguez JE, McCudden CR, Willis MS. Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem. ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  6. TNNT2 gene 
    ... 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
  7. MYBPC3 gene 
    ... do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ... PubMed Central Rodriguez JE, McCudden CR, Willis MS. Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem. ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  8. TTN gene 
    ... TTN gene variants have been found to cause familial dilated cardiomyopathy, a condition that weakens and enlarges the heart, ... from pumping blood efficiently. Signs and symptoms of familial dilated cardiomyopathy typically begin in mid-adulthood and result in ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  9. MYH6 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
  10. DMD gene 
    ... gene can cause an X-linked form of familial dilated cardiomyopathy. This heart condition enlarges and weakens the cardiac ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition BMD DMD_HUMAN ...
    https://medlineplus.gov/genetics/gene/dmd - Genetics
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