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Results 11 - 17 of 17 for Hypertrophic cardiomyopathy 26
  1. 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
  2. Carnitine palmitoyltransferase II deficiency 
    ... CPT II) deficiency. J Inherit Metab Dis. 2003;26(6):543-57. doi: 10.1023/a:1025947930752. ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  3. Mitochondrial complex V deficiency 
    ... Inherit Metab Dis. 2015 May;38(3):417-26. doi: 10.1007/s10545-014-9774-8. Epub ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  4. Glycogen storage disease type 0 
    ... j.ymgme.2009.07.012. Epub 2009 Jul 26. Citation on PubMed Fredriksson J, Anevski D, Almgren ... Forsander G, Jotorp P, Oldfors A, Holme E. Cardiomyopathy and exercise intolerance in muscle glycogen storage disease ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  5. Cardiofaciocutaneous syndrome 
    ... 10.1136/jmg.2007.054460. Epub 2007 Nov 26. Citation on PubMed Gripp KW, Lin AE, Nicholson ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  6. Noonan syndrome 
    ... M, Gelb BD. Noonan syndrome. Lancet. 2013 Jan 26;381(9863):333-42. doi: 10.1016/S0140- ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  7. Triosephosphate isomerase deficiency 
    ... j.bbadis.2009.09.012. Epub 2009 Sep 26. Citation on PubMed Rodriguez-Almazan C, Arreola R, ...
    https://medlineplus.gov/.../triosephosphate-isomerase-deficiency - Genetics
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