Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 21 for Familial hypertrophic cardiomyopathy 8
  1. DSP gene 
    ... HAIR AND KERATODERMA; DCWHK ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8 EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  2. PKP2 gene 
    ... Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA.105.609719. Epub 2006 ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  3. MYBPC3 gene 
    ... filaments. Science. 2012 Sep 7;337(6099):1215-8. doi: 10.1126/science.1223602. Epub 2012 Aug 23. Citation on PubMed or Free article on PubMed Central Rodriguez JE, McCudden CR, Willis MS. Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem. ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  4. FKTN gene 
    ... Novel mutations and genotype-phenotype relationships in 107 families with ... dilated cardiomyopathy with minimal muscle weakness. Ann Neurol. 2006 Nov; ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  5. SCN5A gene 
    ... pointes. Circulation. 2002 Apr 23;105(16):1943-8. doi: 10.1161/01.cir.0000014448.19052.4c. ... Epub 2016 Feb 23. Citation on PubMed
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  6. TNNI3 gene 
    ... do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ... S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  7. MYH7 gene 
    ... do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ... on PubMed Rodriguez JE, McCudden CR, Willis MS. Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem. ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  8. TTN gene 
    ... TTN gene variants have been found to cause familial dilated cardiomyopathy, a condition that weakens and enlarges the heart, ... from pumping blood efficiently. Signs and symptoms of familial dilated cardiomyopathy typically begin in mid-adulthood and result in ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  9. DMD gene 
    ... gene can cause an X-linked form of familial dilated cardiomyopathy. This heart condition enlarges and weakens the cardiac ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition BMD DMD_HUMAN ...
    https://medlineplus.gov/genetics/gene/dmd - Genetics
  10. PRKAG2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial hypertrophic cardiomyopathy More About This Health Condition Several mutations in ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
previous · 1 · 2 · 3 · next