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Results 1 - 10 of 30 for Familial hypertrophic cardiomyopathy 1
  1. PSEN1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition AD3 FAD presenilin 1 (Alzheimer disease 3) presenilin 1 protein PS1 PSN1_ ...
    https://medlineplus.gov/genetics/gene/psen1 - Genetics
  2. TNNT2 gene 
    ... HE, Kern M, Katus HA, Frey N. Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation. Cardiovasc Res. 2010 Jun 1;86(3):452-60. doi: 10.1093/cvr/ ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  3. RYR2 gene 
    ... mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). Hum Mol Genet. 2001 Feb 1;10(3):189-94. doi: 10.1093/hmg/ ...
    https://medlineplus.gov/genetics/gene/ryr2 - Genetics
  4. MYH7 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial restrictive cardiomyopathy More About This Health Condition beta-myosin heavy chain MGC138376 MGC138378 MPD1 MYH7_HUMAN MyHC-beta myhc-slow MYHCB myosin heavy chain (AA 1-96) Myosin heavy chain 7 Myosin heavy chain, ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  5. TNNI3 gene 
    ... AV, Potter JD. Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene. Mol Cell Biochem. 2004 Aug;263(1-2):99-114. doi: 10.1023/B:MCBI. ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  6. SCN5A gene 
    ... SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 5; SCN5A CARDIOMYOPATHY, DILATED, 1E; CMD1E SUDDEN INFANT DEATH SYNDROME VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1 ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10 NCBI Gene ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  7. PSEN2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition AD3-like protein AD3L AD3LP AD4 AD5 Alzheimer's disease 3-like E5-1 presenilin 2 (Alzheimer disease 4) PS2 protein (alzheimer- ...
    https://medlineplus.gov/genetics/gene/psen2 - Genetics
  8. MYBPC3 gene 
    ... J Muscle Res Cell Motil. 2012 May;33(1):81. Carrrier, Lucie [corrected to Carrier, Lucie]. Citation on PubMed Marston SB. How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  9. LAMP2 gene 
    ... LAMP2 gene variant are thought to account for 1 to 4 percent of individuals with hypertrophic cardiomyopathy. More About This Health Condition CD107 antigen-like family member B CD107b LAMP-2 LAMP2_HUMAN LAMPB ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics
  10. MYH6 gene 
    ... 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 ATRIAL ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
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