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Results 1 - 10 of 33 for Hypertrophic cardiomyopathy 6
  1. MYH6 gene 
    ... alpha myosin, heavy polypeptide 6, cardiac muscle, alpha (cardiomyopathy, hypertrophic 1) myosin-6 SSS3 Tests of MYH6 PubMed MYOSIN, HEAVY CHAIN 6, CARDIAC MUSCLE, ALPHA; MYH6 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14; CMH14 CARDIOMYOPATHY, DILATED, 1EE; CMD1EE ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
  2. MYH7 gene 
    ... mutations lead to the features of familial hypertrophic cardiomyopathy. More About This Health Condition At least six mutations in the MYH7 gene have been found ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  3. DSP gene 
    ... mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circ Res. 2006 Sep 15;99(6):646-55. doi: 10.1161/01.RES.0000241482. ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  4. TTN gene 
    ... complex contribution of TTN truncating variants to dilated cardiomyopathy. Circ Cardiovasc Genet. 2013 Apr;6(2):144-53. doi: 10.1161/CIRCGENETICS.111. ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  5. TNNI3 gene 
    ... S, Syrris P, McKenna WJ. Genetics of restrictive cardiomyopathy. Heart Fail Clin. 2010 Apr;6(2):179-86. doi: 10.1016/j.hfc. ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  6. DSC2 gene 
    ... B. Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2006 Dec;79(6):1081-8. doi: 10.1086/509044. Epub 2006 ...
    https://medlineplus.gov/genetics/gene/dsc2 - Genetics
  7. MT-TH gene 
    ... single evolutionary origin as a risk factor for cardiomyopathy. Am J Hum Genet. 2000 Dec;67(6):1617-20. doi: 10.1086/316896. Epub 2000 ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
  8. MT-TV gene 
    ... mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS. Ital Heart J. 2004 Jun;5(6):460-5. Citation on PubMed Taylor RW, Chinnery ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  9. PRKAG2 gene 
    ... Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history. J Am Coll Cardiol. 2005 Mar 15;45(6):922-30. doi: 10.1016/j.jacc.2004. ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  10. MT-TL1 gene 
    ... H, Honzik T, Zeman J, Linhart A. Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an adult male. Int Heart J. 2012;53(6):383-7. doi: 10.1536/ihj.53.383. ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
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