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Results 1 - 10 of 57 for Hypertrophic cardiomyopathy 3
  1. Familial restrictive cardiomyopathy 
    ... Registry: Cardiomyopathy, familial restrictive, 1 Genetic Testing Registry: Cardiomyopathy, familial restrictive, 3 National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  2. Familial hypertrophic cardiomyopathy 
    ... NORD) ClinicalTrials.gov CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 CARDIOMYOPATHY, FAMILIAL ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  3. Dilated cardiomyopathy with ataxia syndrome 
    ... Testing Registry: 3-methylglutaconic aciduria type 5 Dilated cardiomyopathy with ataxia National Organization for Rare Disorders (NORD) ClinicalTrials.gov 3-METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5 PubMed Davey KM, ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  4. Familial dilated cardiomyopathy 
    ... Dellefave L, McNally EM. The genetics of dilated cardiomyopathy. Curr Opin Cardiol. 2010 May;25(3):198-204. doi: 10.1097/HCO.0b013e328337ba52. Citation ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  5. Primary carnitine deficiency 
    ... no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy. Am J Med Genet. 2002 Aug 15;111(3):271-84. doi: 10.1002/ajmg.10585. Citation ...
    https://medlineplus.gov/.../condition/primary-carnitine-deficiency - Genetics
  6. Arrhythmogenic right ventricular cardiomyopathy 
    ... Riele AS, Hauer RN. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: clinical challenges in a changing disease spectrum. Trends Cardiovasc Med. 2015 Apr;25(3):191-8. doi: 10.1016/j.tcm.2014. ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  7. Glycogen storage disease type IV 
    ... only mild muscle weakness while others have severe cardiomyopathy and die in early adulthood. GSD IV is estimated to occur in 1 in 600,000 to 800,000 individuals worldwide. Type IV accounts for roughly 3 percent of all cases of glycogen storage disease. ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  8. Duchenne and Becker muscular dystrophy 
    ... Becker muscular dystrophy. People with X-linked dilated cardiomyopathy typically do not ... muscular dystrophies together affect 1 in 3,500 to 5,000 newborn males worldwide. Between ...
    https://medlineplus.gov/.../duchenne-and-becker-muscular-dystrophy - Genetics
  9. Barth syndrome 
    ... E, Wevers RA. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. J Inherit Metab Dis. 2013 Nov;36(6):923-8. doi: 10.1007/s10545-012-9580-0. Epub 2013 Jan 8. Citation on PubMed
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  10. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... serious heart problems, such as a weakened heart (cardiomyopathy) and heart failure; breathing difficulties; coma; and sudden ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
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