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Results 1 - 10 of 36 for Hypertrophic cardiomyopathy 26
  1. Centronuclear myopathy 
    ... and its deficiency causes centronuclear myopathy with dilated cardiomyopathy. Am J Hum Genet. 2014 Aug 7;95(2):218-26. doi: 10.1016/j.ajhg.2014.07.004. ...
    https://medlineplus.gov/genetics/condition/centronuclear-myopathy - Genetics
  2. MYH7 gene 
    ... Sylvius N, Komajda M. Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. Eur Heart J. 2005 Apr;26(8):794-803. doi: 10.1093/eurheartj/ehi193. ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  3. SLC25A4 gene 
    ... Morton DH, Narula J, Wallace DC. Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup. Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3453-8. doi: 10.1073/pnas. ...
    https://medlineplus.gov/genetics/gene/slc25a4 - Genetics
  4. Heart failure - surgeries and devices 
    ... J Am Coll Cardiol . 2015;65(19):e7-26. PMID: 25861963 pubmed.ncbi.nlm.nih.gov/25861963/ .
    https://medlineplus.gov/ency/patientinstructions/000363.htm - Medical Encyclopedia
  5. TAFAZZIN gene 
    ... syndrome. Mol Genet Metab. 2014 Jan;111(1):26-32. doi: 10.1016/j.ymgme.2013.11. ...
    https://medlineplus.gov/genetics/gene/tafazzin - Genetics
  6. Barth syndrome 
    ... risks, and management. Curr Opin Hematol. 2019 Jan;26(1):6-15. doi: 10.1097/MOH.0000000000000472. ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  7. MT-TL1 gene 
    ... j.nmd.2004.10.002. Epub 2004 Nov 26. Citation on PubMed
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  8. TTN gene 
    ... 500. doi: 10.1086/342380. Epub 2002 Jul 26. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  9. Keratoderma with woolly hair 
    ... 10.1136/jmedgenet-2014-102346. Epub 2014 Mar 26. Citation on PubMed Ramot Y, Zlotogorski A. The ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  10. Glycogen storage disease type IV 
    ... glycogen branching enzyme deficiency. Acta Myol. 2007 Jul;26(1):75-8. Citation on PubMed or Free ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
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