Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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Cardiomyopathy, Hypertrophic, FamilialLegal notice  


Other terms
Cardiomyopathy, Familial Hypertrophic,Cardiomyopathies, Familial Hypertrophic,Familial Hypertrophic Cardiomyopathies,Hypertrophic Cardiomyopathies, Familial,Hypertrophic Cardiomyopathy, Familial,Hereditary Ventricular Hypertrophy,Hereditary Ventricular Hypertrophies,Hypertrophies, Hereditary Ventricular,Hypertrophy, Hereditary Ventricular,Ventricular Hypertrophies, Hereditary,Ventricular Hypertrophy, Familial,Familial Ventricular Hypertrophies,Familial Ventricular Hypertrophy,Hypertrophy, Familial Ventricular,Ventricular Hypertrophies, Familial,Asymmetric Septal Hypertrophy, Familial,Familial Hypertrophic Cardiomyopathy

Description
Cardiomyopathy, Hypertrophic, Familial: An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.



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Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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