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Results 31 - 40 of 112 for Idiopathic cardiomyopathy
  1. JUP gene 
    ... MedlinePlus Genetics provides information about Arrhythmogenic right ventricular cardiomyopathy More About This Health Condition Several mutations in ...
    https://medlineplus.gov/genetics/gene/jup - Genetics
  2. SLC25A4 gene 
    ... cause a disorder characterized by myopathy and hypertrophic cardiomyopathy. Myopathy is weakness of the muscles used for movement, and cardiomyopathy is a thickening of the heart muscle that ...
    https://medlineplus.gov/genetics/gene/slc25a4 - Genetics
  3. MT-TH gene 
    ... the risk of developing a heart condition called cardiomyopathy. People with cardiomyopathy have a weakened heart muscle that is unable ... gene has been identified in several adults with cardiomyopathy, but without other common signs of mitochondrial disease ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
  4. ABCC9 gene 
    ... Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition At least two ... gene have been identified in people with dilated cardiomyopathy, a form of heart disease that enlarges and ...
    https://medlineplus.gov/genetics/gene/abcc9 - Genetics
  5. CAV3 gene 
    ... Condition CAV3 gene mutations also can cause hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy is a thickening of the heart (cardiac) muscle ... failure.When caused by CAV3 gene mutations, hypertrophic cardiomyopathy as well as limb-girdle muscular dystrophy, isolated ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
  6. DOLK-congenital disorder of glycosylation 
    ... CDG develop a weakened and enlarged heart (dilated cardiomyopathy). Other frequent signs and symptoms include recurrent seizures; ... adulthood, often because of complications related to dilated cardiomyopathy, and some do not survive past infancy. DOLK- ...
    https://medlineplus.gov/...dolk-congenital-disorder-of-glycosylation - Genetics
  7. Glycogen storage disease type IV 
    ... needed for breathing. These babies often have dilated cardiomyopathy, which enlarges and weakens the heart (cardiac) muscle, ... childhood and is characterized by myopathy and dilated cardiomyopathy. The severity of this type of GSD IV ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  8. DNAJC19 gene 
    ... DNAJC19 gene have been found to cause dilated cardiomyopathy with ataxia (DCMA) syndrome. This condition is characterized ... mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies. Pediatr Res. ...
    https://medlineplus.gov/genetics/gene/dnajc19 - Genetics
  9. RYR2 gene 
    ... cause a heart condition called arrhythmogenic right ventricular cardiomyopathy (ARVC). This condition causes part of the heart ... WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 NCBI Gene ClinVar Bhuiyan ZA, van den ...
    https://medlineplus.gov/genetics/gene/ryr2 - Genetics
  10. SGCB gene 
    ... 2E also develop a heart condition called dilated cardiomyopathy. Dilated cardiomyopathy is a form of heart disease that enlarges ... muscle, preventing it from pumping blood efficiently. Dilated cardiomyopathy progresses rapidly and is life-threatening in many ...
    https://medlineplus.gov/genetics/gene/sgcb - Genetics
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