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Results 1 - 10 of 25 for Familial hypertrophic cardiomyopathy 6
  1. Familial hypertrophic cardiomyopathy 
    ... 3; CMH3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. 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; ARVD6 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8 ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  3. Familial restrictive cardiomyopathy 
    ... of restrictive cardiomyopathy. Heart Fail Clin. 2010 Apr;6(2):179-86. doi: 10.1016/j.hfc.2009.11.005. Citation on PubMed Xu Q, Dewey S, Nguyen S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  4. Familial partial lipodystrophy 
    ... to hormonal changes.Researchers have described at least six forms of familial ... muscle (cardiomyopathy), a form of heart disease called coronary artery ...
    https://medlineplus.gov/.../condition/familial-partial-lipodystrophy - Genetics
  5. 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
  6. Alström syndrome 
    ... 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
  7. Early-onset myopathy with fatal cardiomyopathy 
    ... Andeejani A, Campbell KP. A novel form of familial congenital muscular dystrophy in two adolescents. Neuropediatrics. 1998 Dec;29(6):289-93. doi: 10.1055/s-2007-973579. ...
    https://medlineplus.gov/...-onset-myopathy-with-fatal-cardiomyopathy - Genetics
  8. Alcohol use disorder 
    ... of inheritance, although many affected individuals have a family history of problems with alcohol or other substances. Children of people with alcohol use disorder are two to six times more likely than the general public to ...
    https://medlineplus.gov/genetics/condition/alcohol-use-disorder - Genetics
  9. Costello syndrome 
    ... this condition have short stature compared to their family and peers and may have ... Neurological problems in people with Costello syndrome include ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  10. Isolated hyperCKemia 
    ... muscle disease, and a heart disorder called hypertrophic cardiomyopathy. Several CAV3 gene mutations have been found ... This condition is inherited in an autosomal ...
    https://medlineplus.gov/genetics/condition/isolated-hyperckemia - Genetics
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