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Results 1 - 9 of 9 for "Cardiomyopathy," familial "hypertrophic," 26
  1. MYH7 gene 
    ... the MYH7 gene are a common cause of familial hypertrophic cardiomyopathy, accounting for up to 35 percent of all ... of the cardiac muscle. Although some people with familial hypertrophic cardiomyopathy have no obvious health effects, all affected individuals ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  2. TTN gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial hypertrophic cardiomyopathy More About This Health Condition TTN gene variants ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  3. SLC25A4 gene 
    ... how deletions of mtDNA lead to myopathy and hypertrophic cardiomyopathy. ... carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 ...
    https://medlineplus.gov/genetics/gene/slc25a4 - Genetics
  4. Noonan syndrome with multiple lentigines 
    ... who have heart defects, about 80 percent have hypertrophic cardiomyopathy, which is a thickening of the heart muscle ... heart to work harder to pump blood. The hypertrophic cardiomyopathy most often affects the lower left chamber of ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  5. ACAD9 deficiency 
    ... also have an enlarged and weakened heart muscle (hypertrophic cardiomyopathy), which is typically fatal in infancy or childhood. ... symptoms of ACAD9 deficiency, such as encephalomyopathy and hypertrophic cardiomyopathy. Although the exact mechanism is unclear, it is ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  6. Mitochondrial complex V deficiency 
    ... common feature of mitochondrial complex V deficiency is hypertrophic cardiomyopathy. This condition is characterized by thickening (hypertrophy) of the heart (cardiac) muscle that can lead ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  7. Cardiofaciocutaneous syndrome 
    ... disease that enlarges and weakens the heart muscle (hypertrophic cardiomyopathy).Cardiofaciocutaneous syndrome is also characterized by distinctive facial ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  8. Noonan syndrome 
    ... to the lungs (pulmonary valve stenosis). Some have hypertrophic cardiomyopathy, which enlarges and weakens the heart muscle.A ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  9. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Living With ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF ... muscular dystrophy; exercise with a disability; neuromuscular ...
    https://www.mda.org/.../files/MDA_Quest_Excercise_Package_2009.pdf - External Health Links