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Results 1 - 10 of 29 for Hypertrophic cardiomyopathy 25
  1. Familial hypertrophic cardiomyopathy 
    ... HYPERTROPHIC, 8; CMH8 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11 CARDIOMYOPATHY, FAMILIAL ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. Familial dilated cardiomyopathy 
    ... CARDIOMYOPATHY, DILATED, 1K; CMD1K CARDIOMYOPATHY, DILATED, 1M; CMD1M CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25 CARDIOMYOPATHY, DILATED, 1P; CMD1P CARDIOMYOPATHY, DILATED, 1Q; ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  3. Left ventricular noncompaction 
    ... Lorts A, Jefferies JL. Left ventricular non-compaction cardiomyopathy. Lancet. 2015 Aug 22;386(9995):813-25. doi: 10.1016/S0140-6736(14)61282-4. ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  4. Arrhythmogenic right ventricular cardiomyopathy 
    ... Riele AS, Hauer RN. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: clinical challenges in a changing disease spectrum. Trends Cardiovasc Med. 2015 Apr;25(3):191-8. doi: 10.1016/j.tcm. ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  5. Congenital fiber-type disproportion 
    ... have a weakened and enlarged heart muscle (dilated cardiomyopathy).The severity of congenital fiber-type disproportion varies widely. It is estimated that up to 25 percent of affected individuals experience severe muscle weakness ...
    https://medlineplus.gov/.../congenital-fiber-type-disproportion - Genetics
  6. Glycogen storage disease type 0 
    ... Forsander G, Jotorp P, Oldfors A, Holme E. Cardiomyopathy and exercise intolerance in ... J Pediatr Endocrinol Metab. 2012;25(9-10):963-7. doi: 10.1515/jpem- ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  7. Alpha-N-acetylgalactosaminidase deficiency 
    ... Eur J Case Rep Intern Med. 2019 Oct 25;6(11):001269. doi: 10.12890/2019_001269. eCollection 2019. Citation on PubMed Chabas A, Duque J, Gort L. A new infantile case of alpha-N-acetylgalactosaminidase deficiency. Cardiomyopathy as a presenting symptom. J Inherit Metab Dis. ...
    https://medlineplus.gov/...lpha-n-acetylgalactosaminidase-deficiency - Genetics
  8. Danon disease 
    ... 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, ...
    https://medlineplus.gov/genetics/condition/danon-disease - Genetics
  9. Barth syndrome 
    ... characterized by an enlarged and weakened heart (dilated cardiomyopathy), weakness in muscles used for movement (skeletal myopathy), ... in males.In males with Barth syndrome, dilated cardiomyopathy is often present at birth or develops within ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  10. Noonan syndrome with multiple lentigines 
    ... have heart defects, about 80 percent have hypertrophic cardiomyopathy, which is a thickening of the heart muscle ... to work harder to pump blood. The hypertrophic cardiomyopathy most often affects the lower left chamber of ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
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