|cardiomyopathy hypertrophic icd 10||1.2||0.4||6416||57|
|cardiomyopathy hypertrophic icd 10 code||1.94||0.5||1784||22|
|septal hypertrophic cardiomyopathy icd 10||0.95||0.4||5804||23|
|primary hypertrophic cardiomyopathy icd 10||0.06||0.2||6360||91|
|congenital hypertrophic cardiomyopathy icd 10||1.02||0.2||676||39|
|apical hypertrophic cardiomyopathy icd 10||1.78||0.6||4082||85|
|other hypertrophic cardiomyopathy icd 10||1.62||0.1||4530||78|
|other hypertrophic cardiomyopathy icd 10 code||1.45||0.8||9514||13|
|icd 10 code for cardiomyopathy hypertrophic||1.3||0.4||9690||78|
Some people with hypertrophic cardiomyopathy may not have symptoms and will have normal lifespan. Others may get worse slowly or quickly. In some cases, the condition may develop into dilated cardiomyopathy. People with hypertrophic cardiomyopathy are at higher risk for sudden death than people without the condition.Can you die of hypertrophic cardiomyopathy?
1-year survival rate for Hypertrophic cardiomyopathy: About 2 to 3 percent die each year because the heart suddenly stops beating. 10-year survival rate for Hypertrophic cardiomyopathy: Over 10 years, the risk of sudden death can be 20 percent or more.Do I have hypertrophic cardiomyopathy?
Hypertrophic cardiomyopathy (HCM) is a complex type of heart disease that affects the heart muscle. It causes thickening of the heart muscle (especially the ventricles, or lower heart chambers), left ventricular stiffness, mitral valve changes and cellular changes. Thickening of the heart muscle (myocardium) occurs most commonly at the septum.