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Results 1 - 10 of 17 for Hypertrophic cardiomyopathy 26
  1. Centronuclear myopathy 
    ... and its deficiency causes centronuclear myopathy with dilated cardiomyopathy. Am J Hum Genet. 2014 Aug 7;95(2):218-26. doi: 10.1016/j.ajhg.2014.07.004. ...
    https://medlineplus.gov/genetics/condition/centronuclear-myopathy - Genetics
  2. Barth syndrome 
    ... risks, and management. Curr Opin Hematol. 2019 Jan;26(1):6-15. doi: 10.1097/MOH.0000000000000472. ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  3. Keratoderma with woolly hair 
    ... 10.1136/jmedgenet-2014-102346. Epub 2014 Mar 26. Citation on PubMed Ramot Y, Zlotogorski A. The ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  4. Glycogen storage disease type IV 
    ... glycogen branching enzyme deficiency. Acta Myol. 2007 Jul;26(1):75-8. Citation on PubMed or Free ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  5. Myoclonic epilepsy with ragged-red fibers 
    ... 1007/s10048-012-0322-0. Epub 2012 May 26. Citation on PubMed Deschauer M, Muller T, Wieser ... j.bbrc.2007.01.099. Epub 2007 Jan 26. Citation on PubMed Melone MA, Tessa A, Petrini ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  6. Glycogen storage disease type VII 
    ... Muscle glycogenoses: an overview. Acta Myol. 2007 Jul;26(1):35-41. No abstract available. Citation on ... clinical and genetic update. Acta Myol. 2007 Oct;26(2):105-7. Citation on PubMed or Free ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-vii - Genetics
  7. ACAD9 deficiency 
    ... doi: 10.1093/hmg/ddv074. Epub 2015 Feb 26. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  8. Noonan syndrome with multiple lentigines 
    ... diagnosis of RASopathies. BMC Med Genet. 2014 Apr 26;15:44. doi: 10.1186/1471-2350-15- ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  9. Malonyl-CoA decarboxylase deficiency 
    ... J Hum Genet. 1999 Aug;65(2):318-26. doi: 10.1086/302492. Citation on PubMed or ...
    https://medlineplus.gov/.../malonyl-coa-decarboxylase-deficiency - Genetics
  10. Primary carnitine deficiency 
    ... known molecular defects. J Inherit Metab Dis. 2003;26(2-3):147-69. doi: 10.1023/a: ...
    https://medlineplus.gov/.../condition/primary-carnitine-deficiency - Genetics
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