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Results 1 - 10 of 18 for Familial hypertrophic cardiomyopathy 24
  1. PKP2 gene 
    ... WJ. Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy. Circulation. 2006 Jan 24;113(3):356-64. doi: 10.1161/CIRCULATIONAHA. ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  2. Familial restrictive cardiomyopathy 
    ... 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
  3. 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
  4. PSEN2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition AD3-like protein ...
    https://medlineplus.gov/genetics/gene/psen2 - Genetics
  5. PSEN1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition AD3 FAD presenilin ...
    https://medlineplus.gov/genetics/gene/psen1 - Genetics
  6. 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
  7. 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
  8. LAMP2 gene 
    ... Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease). Nature. 2000 Aug 24;406(6798):906-10. doi: 10.1038/35022604. ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics
  9. Wolff-Parkinson-White syndrome 
    ... Hassan AS]. N Engl J Med 2002 Jan 24;346(4):300. Citation on PubMed Light PE. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  10. JUP gene 
    ... a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). Lancet. 2000 Jun 17;355(9221):2119-24. doi: 10.1016/S0140-6736(00)02379-5. ...
    https://medlineplus.gov/genetics/gene/jup - Genetics
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