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Results 1 - 10 of 15 for Familial hypertrophic cardiomyopathy 20
  1. Familial hypertrophic cardiomyopathy 
    ... 17; CMH17 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9; CMH9 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. Familial dilated cardiomyopathy 
    ... Mutations in one gene, TTN, account for approximately 20 percent of cases of familial dilated cardiomyopathy. The TTN gene provides instructions for making a ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  3. Familial restrictive cardiomyopathy 
    ... S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  4. Arrhythmogenic right ventricular cardiomyopathy 
    ... WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6; ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  5. Noonan syndrome with multiple lentigines 
    ... to work harder to pump blood. The hypertrophic cardiomyopathy most often affects the lower left chamber of the heart (the left ventricle). Up to 20 percent of people with Noonan syndrome with multiple ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  6. 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
  7. ACAD9 deficiency 
    ... dehydrogenase 9 deficiency Deficiency of acyl-CoA dehydrogenase family member 9 Mitochondrial complex I deficiency due to ACAD9 deficiency ... PubMed Aintablian HK, Narayanan V, Belnap N, ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  8. Alcohol use disorder 
    ... influences that are shared by members of a family. Alcohol addiction Alcohol dependence Alcoholism ... Abrahao KP, Salinas AG, Lovinger DM. Alcohol and the Brain: Neuronal Molecular Targets, Synapses, and Circuits. Neuron. 2017 Dec 20;96(6):1223-1238. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/condition/alcohol-use-disorder - Genetics
  9. 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
  10. Cytochrome c oxidase deficiency 
    ... affected individuals, even among those in the same family. People who are mildly ... cardiomyopathy). Another possible feature of this condition is an ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
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