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facts about Cardiomyopathy, familial hypertrophic

Cardiomyopathy, familial hypertrophic

Cardiomyopathy, familial hypertrophic (an autosomal dominant inherited form of hypertrophic cardiomyopathy)

medical condition, medical concept, cause, Autosomal dominant conditions
Symptoms
fourth heart sound, Rapid up-stroke pulse, Chest pain, Syncope, Cardiac arrest,  …
Class
medical condition, Autosomal dominant conditions, medical concept, cause
Cause of
atrial fibrillation, hypertrophic cardiomyopathy, Chest pain, Syncope, left ventricular hypertrophy,  …
Allelic with
Myosin storage myopathy, Laing distal myopathy
Mesh ID
"D024741"
Diseases DB id
"6374"
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The prevalence of HCM is about 0.2% to 0.5% of the general population. Myosin heavy chain mutations are associated with development of familial hypertrophic cardiomyopathy.
Familial hypertrophic cardiomyopathy ORDR lists rare diseases for information ... in rare diseases, GARD's How to Find an Expert fact ... Clinical Research for Rare Diseases, October 2 ...
Familial hypertrophic cardiomyopathy: A genetic disorder of the heart characterized by increased growth ... arrest over 20 years whereas those with a wall thickness more than 1.2 ...
In hypertrophic cardiomyopathy, the heart muscle cells become enlarged. In fact ... Hypertrophic cardiomyopathy occurs in no more than 2 out ... for familial hypertrophic cardiomyopathy ...
Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is ... In fact, HCM is the leading cause of sudden ... HCM is a familial disease. [2] There are defects in several ...

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