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Results 1 - 10 of 211 for Hypertrophic cardiomyopathy 2
  1. Familial hypertrophic cardiomyopathy 
    ... Registry: Hypertrophic cardiomyopathy 1 Genetic Testing Registry: Hypertrophic cardiomyopathy 2 Genetic Testing Registry: Hypertrophic cardiomyopathy 4 Genetic Testing ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. PKP2 gene 
    ... Creason V, Wahl JK 3rd. Arrhythmogenic right ventricular cardiomyopathy plakophilin-2 mutations disrupt desmosome assembly and stability. Cell Commun ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  3. RYR2 gene 
    ... gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). Hum Mol Genet. 2001 Feb 1;10( ...
    https://medlineplus.gov/genetics/gene/ryr2 - Genetics
  4. Familial restrictive cardiomyopathy 
    ... RESTRICTIVE, 1; RCM1 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 2; RCM2 PubMed Elliott P, Andersson B, Arbustini E, ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  5. TAFAZZIN gene 
    ... BTHS CMD3A EFE EFE2 G4.5 LVNCX tafazzin (cardiomyopathy, dilated 3A (X-linked); endocardial fibroelastosis 2; Barth syndrome) TAZ_HUMAN XAP-2 Tests of ...
    https://medlineplus.gov/genetics/gene/tafazzin - Genetics
  6. DSC2 gene 
    ... McKenna WJ. Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations. Cardiovasc Res. 2011 Apr 1;90(1): ...
    https://medlineplus.gov/genetics/gene/dsc2 - Genetics
  7. Alström syndrome 
    ... that enlarges and weakens the heart muscle (dilated cardiomyopathy), obesity, type 2 diabetes (the most common form of diabetes), and ... JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom ... review. Orphanet J Rare Dis. 2007 Dec 21;2:49. doi: 10.1186/1750-1172-2-49. ...
    https://medlineplus.gov/genetics/condition/alstrom-syndrome - Genetics
  8. TNNT2 gene 
    ... of TNNT2 mutations identified in patients with dilated cardiomyopathy. Circ Cardiovasc Genet. 2009 Aug;2(4):306-13. doi: 10.1161/CIRCGENETICS.108. ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl ... Epub 2011 Mar 22. Citation on PubMed Otten ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  9. TNNI3 gene 
    ... C, Nallari P. Molecular genetics of familial hypertrophic cardiomyopathy (FHC). J Hum Genet. 2003;48(2):55-64. doi: 10.1007/s100380300007. Citation on ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  10. TTN gene 
    ... the giant muscle filament titin, cause familial dilated cardiomyopathy. Nat Genet. 2002 Feb;30(2):201-4. doi: 10.1038/ng815. Epub 2002 ... complex contribution of TTN truncating variants to dilated cardiomyopathy. Circ Cardiovasc Genet. 2013 Apr;6(2):144-53. doi: 10.1161/CIRCGENETICS.111.000062. ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
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