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Results 1 - 10 of 63 for Dilated cardiomyopathy 1S
  1. Familial hypertrophic cardiomyopathy 
    ... stenosis Subaortic hypertrophic stenosis Genetic Testing Registry: Hypertrophic cardiomyopathy 1 Genetic Testing Registry: Hypertrophic cardiomyopathy 2 Genetic Testing ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. Familial dilated cardiomyopathy 
    ... CARDIOMYOPATHY, DILATED, 1EE; CMD1EE CARDIOMYOPATHY, DILATED, 1R; CMD1R CARDIOMYOPATHY, DILATED, 1S; CMD1S CARDIOMYOPATHY, DILATED, 1JJ; CMD1JJ CARDIOMYOPATHY, DILATED, 1HH; ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  3. Familial restrictive cardiomyopathy 
    ... Testing Registry: Familial restrictive cardiomyopathy Genetic Testing Registry: Cardiomyopathy, familial restrictive, 1 Genetic Testing Registry: Cardiomyopathy, familial restrictive, 3 National ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  4. Left ventricular noncompaction 
    ... VENTRICULAR NONCOMPACTION 10; LVNC10 CARDIOMYOPATHY, DILATED, 1R; CMD1R CARDIOMYOPATHY, DILATED, 1S; CMD1S LEFT VENTRICULAR NONCOMPACTION 7; LVNC7 PubMed Bennett ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  5. Arrhythmogenic right ventricular cardiomyopathy 
    ... D, Link MS, Calkins H. Arrhythmogenic Right Ventricular Cardiomyopathy. N Engl J Med. 2017 Jan 5;376(1):61-72. doi: 10.1056/NEJMra1509267. No abstract ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  6. Keratoderma with woolly hair 
    ... disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum Mol Genet. 2000 Nov 1;9(18):2761-6. doi: 10.1093/hmg/ ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  7. Mucolipidosis III alpha/beta 
    ... of mucolipidosis III associated with sensory neuropathy and cardiomyopathy. Am J Med Genet A. 2005 Feb 1;132A(4):369-75. doi: 10.1002/ajmg. ...
    https://medlineplus.gov/.../condition/mucolipidosis-iii-alpha-beta - Genetics
  8. Schindler disease 
    ... new infantile case of alpha-N-acetylgalactosaminidase deficiency. Cardiomyopathy as a presenting symptom. J Inherit Metab Dis. 2007 Feb;30(1):108. doi: 10.1007/s10545-006-0470-1. ...
    https://medlineplus.gov/genetics/condition/schindler-disease - Genetics
  9. 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. ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  10. Alström syndrome 
    ... JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs. Am J Med Genet A. 2005 May 15;135(1):96-8. doi: 10.1002/ajmg.a.30688. ...
    https://medlineplus.gov/genetics/condition/alstrom-syndrome - Genetics
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