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Results 1 - 10 of 20 for "Cardiomyopathy," mitochondrial
  1. Multiple mitochondrial dysfunctions syndrome 
    ... pulmonary hypertension) or weakening of the heart muscle (cardiomyopathy). Multiple mitochondrial dysfunctions syndrome is a rare condition; its prevalence ...
    https://medlineplus.gov/...tiple-mitochondrial-dysfunctions-syndrome - Genetics
  2. Mitochondrial trifunctional protein deficiency 
    ... R, Mayatepek E, Bueltmann B, Korenke C. Intrauterine cardiomyopathy and cardiac mitochondrial proliferation in mitochondrial trifunctional protein (TFP) deficiency. Mol ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  3. Mitochondrial complex V deficiency 
    ... damage to other organs.Another common feature of mitochondrial complex V deficiency is hypertrophic cardiomyopathy. This condition is characterized by thickening (hypertrophy) of ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  4. Mitochondrial complex III deficiency 
    ... individuals have a form of heart disease called cardiomyopathy, which can lead to heart failure. Most people with mitochondrial complex III deficiency have a buildup of a ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  5. Dilated cardiomyopathy with ataxia syndrome 
    ... R, Suomalainen A, Tyni T. New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies. Pediatr Res. ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  6. 2-hydroxyglutaric aciduria 
    ... of D-2-hydroxyglutarate may be associated with cardiomyopathy in some people with this form of the condition.The SLC25A1 gene provides instructions for making a protein that transports certain molecules, such as citrate, in and out of mitochondria. Mutations in the SLC25A1 gene reduce the protein' ...
    https://medlineplus.gov/.../condition/2-hydroxyglutaric-aciduria - Genetics
  7. Myoclonic epilepsy with ragged-red fibers 
    ... and a form of heart disease known as cardiomyopathy. Less commonly, people with MERRF ... of a group of conditions known as mitochondrial disorders, which affect an estimated 1 in 5, ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  8. Barth syndrome 
    ... characterized by an enlarged and weakened heart (dilated cardiomyopathy), weakness in muscles used for movement (skeletal myopathy), ... in males.In males with Barth syndrome, dilated cardiomyopathy is often present at birth or develops within ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  9. SUCLG1-related mitochondrial DNA depletion syndrome 
    ... abnormalities and thickening of the heart muscle (hypertrophic cardiomyopathy). In affected individuals, a substance called methylmalonic acid ... ligase. This enzyme plays an important role in mitochondria, which are the energy-producing centers inside the ...
    https://medlineplus.gov/...ated-mitochondrial-dna-depletion-syndrome - Genetics
  10. Cytochrome c oxidase deficiency 
    ... that enlarges and weakens the heart muscle (hypertrophic cardiomyopathy). Another possible feature of this condition is an ... include loss of mental function, movement problems, hypertrophic cardiomyopathy, eating difficulties, and brain abnormalities. Cytochrome c oxidase ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
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