Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 45 for cardiomyopathy
  1. MYH6 gene 
    ... Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition Mutations in the ... cause two diseases of the cardiac muscle, dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM). DCM weakens and ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
  2. 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
  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. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. DES gene 
    ... more likely to have a weakened heart muscle (cardiomyopathy) than people with myofibrillar myopathy caused by mutations in other genes. In some cases, cardiomyopathy is the first symptom of this condition. More ...
    https://medlineplus.gov/genetics/gene/des - Genetics
  10. TNNT2 gene 
    ... in the TNNT2 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/tnnt2 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · next