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Results 1 - 10 of 47 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. HADHA gene 
    ... R, Mayatepek E, Bueltmann B, Korenke C. Intrauterine cardiomyopathy and cardiac mitochondrial proliferation in mitochondrial trifunctional protein (TFP) deficiency. Mol ...
    https://medlineplus.gov/genetics/gene/hadha - Genetics
  4. MT-TL1 gene 
    ... H, Honzik T, Zeman J, Linhart A. Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  5. MT-TK gene 
    ... alteration in the MT-TK gene results in cardiomyopathy, hearing loss, and other symptoms. mitochondrial tRNA-Lys MTTK trnK Tests of MT-TK ... Baram TZ, Madrid RE, DiMauro S. Maternally inherited cardiomyopathy and ... mutation in the mitochondrial tRNA(Lys) gene (G8363A). Am J Hum Genet. ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  6. MT-TH gene 
    ... gene has been identified in several adults with cardiomyopathy, but without other common signs of mitochondrial disease such as neurological abnormalities. This mutation replaces ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
  7. SLC25A4 gene 
    ... muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy. Hum Mol Genet. 2005 Oct 15;14(20):3079-88. doi: 10.1093/hmg/ddi341. Epub 2005 Sep 9. Citation on PubMed ... 1 (ANT1): a new factor in mitochondrial disease. IUBMB Life. 2005 Sep;57(9):607- ...
    https://medlineplus.gov/genetics/gene/slc25a4 - Genetics
  8. What Is Mitochondrial Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... Muscular Dystrophy Association ... PDF
    https://www.mda.org/...tochondrial_Disease_Fact_Sheet_March_2020.pdf - External Health Links
  9. DNAJC19 gene 
    ... 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/genetics/gene/dnajc19 - Genetics
  10. 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
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