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Results 1 - 10 of 28 for Familial hypertrophic cardiomyopathy 3
  1. Familial restrictive cardiomyopathy 
    ... ClinicalTrials.gov CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1; RCM1 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 2; RCM2 PubMed Elliott P, Andersson ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  2. Familial hypertrophic cardiomyopathy 
    ... ClinicalTrials.gov CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  3. Arrhythmogenic right ventricular cardiomyopathy 
    ... Arrhythmogenic right ventricular dysplasia 9 Arrhythmogenic right ... RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4 ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  4. Familial dilated cardiomyopathy 
    Familial dilated cardiomyopathy is a genetic form of heart disease. It occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  5. Familial partial lipodystrophy 
    ... gov LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; FPLD2 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1; FPLD1 LIPODYSTROPHY, ...
    https://medlineplus.gov/.../condition/familial-partial-lipodystrophy - Genetics
  6. Isolated hyperCKemia 
    ... Olive M. A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia. Neuromuscul Disord. 2004 May;14(5):321-4. doi: 10.1016/j.nmd.2004.01.006. Citation on PubMed Carbone ... partial caveolin-3 deficiency and hyperCKemia. Neurology. 2000 Mar 28;54( ...
    https://medlineplus.gov/genetics/condition/isolated-hyperckemia - Genetics
  7. Noonan syndrome with multiple lentigines 
    ... 1; LPRD1 LEOPARD SYNDROME 2; LPRD2 LEOPARD SYNDROME 3; LPRD3 PubMed Kato H, Yoshida R, Tsukamoto K, Suga H, Eto H, Higashino T, Araki J, Ogata T, Yoshimura K. Familial cases of atypical clinical features genetically diagnosed as ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  8. Early-onset myopathy with fatal cardiomyopathy 
    ... Disorders. J Neuromuscul Dis. 2016 Aug 30;3(3):293-308. doi: 10.3233/JND-160158. Citation on PubMed or Free ... Citation on PubMed
    https://medlineplus.gov/...-onset-myopathy-with-fatal-cardiomyopathy - Genetics
  9. Costello syndrome 
    ... this condition have short stature compared to their family and peers and may have ... Neurological problems in people with Costello syndrome include ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  10. Rippling muscle disease 
    ... isolated hyperCKemia, and a heart disorder called hypertrophic cardiomyopathy. ... within the same family.Some people with rippling muscle disease do not ...
    https://medlineplus.gov/genetics/condition/rippling-muscle-disease - Genetics
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