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Results 11 - 20 of 112 for Idiopathic cardiomyopathy
  1. TAFAZZIN gene 
    ... males and is characterized by a weakened heart (cardiomyopathy), muscle weakness, recurrent infections, and short stature. TAFAZZIN ... Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/tafazzin - Genetics
  2. 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
  3. MT-TL1 gene 
    ... muscle is also weakened, which is known as cardiomyopathy. This abnormality prevents the heart from pumping normally. ... H, Honzik T, Zeman J, Linhart A. Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C> ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  4. Geleophysic dysplasia 
    Geleophysic dysplasia is an inherited condition that affects many parts of the body. It is characterized by abnormalities involving the bones, joints, heart, and ...
    https://medlineplus.gov/genetics/condition/geleophysic-dysplasia - Genetics
  5. TNNI3 gene 
    ... in the TNNI3 gene can cause familial hypertrophic cardiomyopathy, a condition characterized by thickening (hypertrophy) of the ... with this condition. Although some people with hypertrophic cardiomyopathy have no obvious health effects, all affected individuals ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  6. TTN gene 
    ... in people with early-onset myopathy with fatal cardiomyopathy (EOMFC), an inherited disease that affects both skeletal ... and a form of heart disease called dilated cardiomyopathy. More About This Health Condition Many TTN gene ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  7. MYH7 gene 
    ... gene are a common cause of familial hypertrophic cardiomyopathy, accounting for up to 35 percent of all ... cardiac muscle. Although some people with familial hypertrophic cardiomyopathy have no obvious health effects, all affected individuals ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  8. DSP gene 
    ... form of heart disease called dilated left ventricular cardiomyopathy.The DSP gene mutations that cause keratoderma with ... that abnormal cell signaling may also contribute to cardiomyopathy in people with this condition. More About This ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  9. Keratoderma with woolly hair 
    ... the feet to become thick, scaly, and calloused.Cardiomyopathy, which is a disease of the heart muscle, ... features of this condition, signs and symptoms of cardiomyopathy may not appear until adolescence or later. Complications ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  10. DMD gene 
    ... wasting (atrophy) and a heart condition called dilated cardiomyopathy. Most of the mutations that cause these conditions ... cause an X-linked form of familial dilated cardiomyopathy. This heart condition enlarges and weakens the cardiac ...
    https://medlineplus.gov/genetics/gene/dmd - Genetics
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