Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 36 for Hypertrophic cardiomyopathy 11
  1. Familial hypertrophic cardiomyopathy 
    ... HYPERTROPHIC, 10; CMH10 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12; CMH12 CARDIOMYOPATHY, FAMILIAL ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. Keratoderma with woolly 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
  3. Arrhythmogenic right ventricular cardiomyopathy 
    ... MacLeod H, Dellefave-Castillo L. Arrhythmogenic Right Ventricular Cardiomyopathy Overview. 2005 Apr 18 [updated 2023 May 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  4. Familial restrictive cardiomyopathy 
    ... Deanfield JE, McKenna WJ, Elliott PM. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes. Heart. 2008 Nov;94(11):1478-84. doi: 10.1136/hrt.2007.134684. ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  5. Familial dilated cardiomyopathy 
    ... Siegfried JD. Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals. Genet Med. 2010 Nov;12(11):655-67. doi: 10.1097/GIM.0b013e3181f2481f. Citation ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  6. Glycogen storage disease type 0 
    ... Forsander G, Jotorp P, Oldfors A, Holme E. Cardiomyopathy and exercise intolerance in muscle glycogen storage disease 0. N Engl J Med. 2007 Oct 11;357(15):1507-14. doi: 10.1056/NEJMoa066691. ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  7. Left ventricular noncompaction 
    ... to Diagnosis and Management of Left Ventricular Noncompaction Cardiomyopathy: Review of the Literature. Cardiol Res Pract. 2016;2016:5172308. doi: 10.1155/2016/5172308. Epub 2016 Jan 11. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  8. Early-onset myopathy with fatal cardiomyopathy 
    ... cause a novel early-onset myopathy with fatal cardiomyopathy. Ann Neurol. 2007 ... 2012 Jan 12 [updated 2019 Apr 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/...-onset-myopathy-with-fatal-cardiomyopathy - Genetics
  9. Alpha-N-acetylgalactosaminidase deficiency 
    ... Case Rep Intern Med. 2019 Oct 25;6(11):001269. doi: 10.12890/2019_001269. eCollection 2019. Citation on PubMed Chabas A, Duque J, Gort L. A new infantile case of alpha-N-acetylgalactosaminidase deficiency. Cardiomyopathy as a presenting symptom. J Inherit Metab Dis. ...
    https://medlineplus.gov/...lpha-n-acetylgalactosaminidase-deficiency - Genetics
  10. ALG12-congenital disorder of glycosylation 
    ... 11(19):2331-9. doi: 10.1093/hmg/11.19.2331. Citation on PubMed Kranz ... cardiomyopathy, genital malformations, and early lethality. Am J Med ...
    https://medlineplus.gov/...lg12-congenital-disorder-of-glycosylation - Genetics
previous · 1 · 2 · 3 · 4 · next