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Results 1 - 10 of 25 for Hypertrophic cardiomyopathy 14
  1. Familial hypertrophic cardiomyopathy 
    ... HYPERTROPHIC, 7; CMH7 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14; CMH14 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15; CMH15 CARDIOMYOPATHY, FAMILIAL ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. Arrhythmogenic right ventricular cardiomyopathy 
    ... ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy. Eur J Heart Fail. 2012 Nov;14(11):1199-207. doi: 10.1093/eurjhf/hfs119. ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  3. Left ventricular noncompaction 
    ... J, Stollberger C, Towbin JA. Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors. Nat Rev Cardiol. 2017 Apr;14(4):224-237. doi: 10.1038/nrcardio.2016. ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  4. Glycogen storage disease type 0 
    ... Forsander G, Jotorp P, Oldfors A, Holme E. Cardiomyopathy and exercise intolerance in muscle glycogen storage disease 0. N Engl J Med. 2007 Oct 11;357(15):1507-14. doi: 10.1056/NEJMoa066691. Citation on PubMed Nessa ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  5. Schindler disease 
    ... new infantile case of alpha-N-acetylgalactosaminidase deficiency. Cardiomyopathy as a presenting symptom. J Inherit Metab Dis. 2007 Feb;30(1):108. doi: 10.1007/s10545-006-0470-1. Epub 2006 Dec 14. Citation on PubMed Clark NE, Garman SC. The ...
    https://medlineplus.gov/genetics/condition/schindler-disease - Genetics
  6. Transthyretin amyloidosis 
    ... therapeutical strategies. Expert Rev Mol Med. 2002 May 14;4(12):1-11. doi: 10.1017/S1462399402004647. ...
    https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis - Genetics
  7. Catecholaminergic polymorphic ventricular tachycardia 
    ... WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2 PubMed ... International Calmodulinopathy Registry. Eur Heart J. 2019 Sep 14;40(35):2964-2975. doi: 10.1093/eurheartj/ ...
    https://medlineplus.gov/...ergic-polymorphic-ventricular-tachycardia - Genetics
  8. 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
  9. 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
  10. Myhre syndrome 
    ... that surrounds the heart (pericarditis), and rarely, restrictive cardiomyopathy, in which the heart muscle is stiff and ... 10.1002/ajmg.a.61430. Epub 2019 Dec 14. Erratum In: Am J Med Genet A. 2024 ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
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