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Results 11 - 20 of 61 for Dilated cardiomyopathy 1S
  1. Catecholaminergic polymorphic ventricular tachycardia 
    ... Disorders (NORD) ClinicalTrials.gov VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2 PubMed ...
    https://medlineplus.gov/...ergic-polymorphic-ventricular-tachycardia - Genetics
  2. Primary coenzyme Q10 deficiency 
    ... that enlarges and weakens the heart muscle (hypertrophic cardiomyopathy) can also occur in primary coenzyme Q10 deficiency. The prevalence of primary coenzyme Q10 deficiency is thought to be less than 1 in 100,000 people. Primary coenzyme Q10 deficiency ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  3. Multiple mitochondrial dysfunctions syndrome 
    ... pulmonary hypertension) or weakening of the heart muscle (cardiomyopathy). ... Multiple mitochondrial dysfunctions ...
    https://medlineplus.gov/...tiple-mitochondrial-dysfunctions-syndrome - Genetics
  4. Glycogen storage disease type III 
    ... people with GSDIIIa have a weakened heart muscle (cardiomyopathy), but affected individuals usually do not experience heart failure. Other people affected with GSDIIIa have no cardiac muscle problems. The incidence of GSDIII in the United States is 1 in 100,000 individuals. This condition is seen ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iii - Genetics
  5. Dilated cardiomyopathy with ataxia syndrome 
    ... new? J Inherit Metab Dis. 2012 Jan;35(1):13-22. doi: 10.1007/s10545-010-9210-7. Epub 2010 Sep 30. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  6. Familial partial lipodystrophy 
    ... muscle weakness (myopathy), abnormalities of the heart muscle (cardiomyopathy), a form of heart ... is a rare disease, affecting an estimated 1 in 1 million people overall. Type 2 is ...
    https://medlineplus.gov/.../condition/familial-partial-lipodystrophy - Genetics
  7. Duchenne and Becker muscular dystrophy 
    ... Becker muscular dystrophy. People with X-linked dilated cardiomyopathy typically do not ... Duchenne and Becker muscular dystrophies together affect 1 in 3,500 to 5,000 newborn males ...
    https://medlineplus.gov/.../duchenne-and-becker-muscular-dystrophy - Genetics
  8. Myoclonic epilepsy with ragged-red fibers 
    ... and a form of heart disease known as cardiomyopathy. Less commonly, people with MERRF develop fatty tumors, ... worldwide. Mutations in the ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  9. Cytochrome c oxidase deficiency 
    ... include loss of mental function, movement problems, hypertrophic cardiomyopathy, eating ... deficiency is estimated to occur in 1 in 35,000 individuals. The prevalence of this ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  10. Congenital fiber-type disproportion 
    ... have a weakened and enlarged heart muscle (dilated cardiomyopathy).The ... condition appear by age 1. The first signs of this condition are usually ...
    https://medlineplus.gov/.../congenital-fiber-type-disproportion - Genetics
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