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.
推出的年份: 2002
树号: C14.280.238.100.500, C14.280.484.048.750.070.160.500, C16.320.160
MeSH 单一 ID: D024741
进入的组:
Cardiomyopathy, Familial Hypertrophic
Cardiomyopathies, Familial Hypertrophic
Familial Hypertrophic Cardiomyopathies
Hypertrophic Cardiomyopathies, Familial
Hypertrophic Cardiomyopathy, Familial
Ventricular Hypertrophy, Hereditary
Asymmetric Septal Hypertrophy, Familial
Hereditary Ventricular Hypertrophy
Hereditary Ventricular Hypertrophies
Hypertrophies, Hereditary Ventricular
Hypertrophy, Hereditary Ventricular
Ventricular Hypertrophies, Hereditary
Familial Hypertrophic Cardiomyopathy
Ventricular Hypertrophy, Familial
Familial Ventricular Hypertrophies
Familial Ventricular Hypertrophy
Hypertrophy, Familial Ventricular
Ventricular Hypertrophies, Familial
Obstructive Asymmetric Septal Hypertrophy
Hypertrophic Subaortic Stenosis, Idiopathic
早前的内容:
Cardiomyopathy, Hypertrophic/genetics (1983-2001)
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