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Results 1 - 10 of 30 for Familial hypertrophic cardiomyopathy 2
  1. Familial hypertrophic cardiomyopathy 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. 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
  3. Familial partial lipodystrophy 
    ... their genetic cause. The most common form of familial partial lipodystrophy ... muscle (cardiomyopathy), a form of heart disease called coronary artery ...
    https://medlineplus.gov/.../condition/familial-partial-lipodystrophy - Genetics
  4. Familial dilated cardiomyopathy 
    ... X chromosomes), a mutation in one of the two copies of the gene in each cell increases the risk of developing heart disease, but females with such a mutation may not develop familial dilated cardiomyopathy. In males (who have only one X chromosome), ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  5. Alström syndrome 
    ... metabolic disorders. Nat Rev Endocrinol. 2011 Feb;7(2):77-88. doi: 10.1038/nrendo.2010.210. Epub 2010 Dec 7. Citation on PubMed Hoffman JD, Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs. ...
    https://medlineplus.gov/genetics/condition/alstrom-syndrome - Genetics
  6. Catecholaminergic polymorphic ventricular tachycardia 
    ... by catecholamines Catecholamine-induced polymorphic ventricular tachycardia CPVT Familial polymorphic ventricular tachycardia FPVT ... PubMed ...
    https://medlineplus.gov/...ergic-polymorphic-ventricular-tachycardia - Genetics
  7. 2-hydroxyglutaric aciduria 
    ... with no history of the condition in their family. 2-HGA Genetic Testing Registry: D-2-hydroxyglutaric aciduria ...
    https://medlineplus.gov/.../condition/2-hydroxyglutaric-aciduria - Genetics
  8. Keratoderma with woolly hair 
    ... HAIR AND KERATODERMA; DCWHK ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  9. Left ventricular noncompaction 
    ... LEFT VENTRICULAR NONCOMPACTION 1; LVNC1 LEFT VENTRICULAR NONCOMPACTION 2; LVNC2 CARDIOMYOPATHY, DILATED, 1Y; CMD1Y LEFT VENTRICULAR NONCOMPACTION 8; LVNC8 ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  10. Arrhythmogenic right ventricular cardiomyopathy 
    ... WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6; ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
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