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Results 1 - 10 of 27 for Hypertrophic cardiomyopathy 20
  1. Familial hypertrophic cardiomyopathy 
    ... HYPERTROPHIC, 17; CMH17 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9; CMH9 CARDIOMYOPATHY, FAMILIAL ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. X-linked dilated cardiomyopathy 
    ... expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy. Circulation. 1997 May 20;95(10):2344-7. doi: 10.1161/01. ... explains the pathogenesis of 5' X-linked dilated cardiomyopathy. BMC Med Genet. 2012 Mar 28;13:20. doi: 10.1186/1471-2350-13-20. Citation ...
    https://medlineplus.gov/.../x-linked-dilated-cardiomyopathy - Genetics
  3. Familial restrictive cardiomyopathy 
    ... Citation on PubMed Mogensen J, Arbustini E. Restrictive cardiomyopathy. Curr Opin Cardiol. 2009 May;24(3):214-20. doi: 10.1097/hco.0b013e32832a1d2e. No abstract available. ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  4. Familial dilated cardiomyopathy 
    ... Mutations in one gene, TTN, account for approximately 20 percent of cases of familial dilated cardiomyopathy. The TTN gene provides instructions for making a ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  5. Arrhythmogenic right ventricular cardiomyopathy 
    ... doi: 10.1093/eurjhf/hfs119. Epub 2012 Jul 20. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  6. Noonan syndrome with multiple lentigines 
    ... to work harder to pump blood. The hypertrophic cardiomyopathy most often affects the lower left chamber of the heart (the left ventricle). Up to 20 percent of people with Noonan syndrome with multiple ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  7. Transthyretin amyloidosis 
    ... individuals with this condition, typically ranging from age 20 to 70. There are two major forms of ...
    https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis - Genetics
  8. 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
  9. Glycogen storage disease type IV 
    ... needed for breathing. These babies often have dilated cardiomyopathy, which enlarges and weakens the heart (cardiac) muscle, ... childhood and is characterized by myopathy and dilated cardiomyopathy. The severity of this type of GSD IV ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  10. Centronuclear myopathy 
    ... with centronuclear myopathy have a weakened heart muscle (cardiomyopathy), disturbances in nerve function (neuropathy), or intellectual disability. ... and its deficiency causes centronuclear myopathy with dilated cardiomyopathy. Am J Hum Genet. 2014 Aug 7;95( ...
    https://medlineplus.gov/genetics/condition/centronuclear-myopathy - Genetics
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