cardiomyopathy, familial hypertrophic, type 7

A phenotypically variable hereditary heart disorder (OMIM:613690) characterised by asymmetic ventricular hypertrophy.
Clinical findings
Dyspnoea, syncope, collapse, palpitations, and chest pain triggered by exercise. The disorder has inter- and intrafamilial variability, ranging from benign and asymptomatic to malignant with high risk of cardiac failure and sudden cardiac death.
Molecular pathology
Caused by defects of TNNI3, which encodes type-3 troponin I protein, TnI-cardiac (exclusively expressed in heart muscle).

单词	cardiomyopathy, familial hypertrophic, type 7
释义	cardiomyopathy, familial hypertrophic, type 7 cardiomyopathy, familial hypertrophic, type 7 A phenotypically variable hereditary heart disorder (OMIM:613690) characterised by asymmetic ventricular hypertrophy. Clinical findings Dyspnoea, syncope, collapse, palpitations, and chest pain triggered by exercise. The disorder has inter- and intrafamilial variability, ranging from benign and asymptomatic to malignant with high risk of cardiac failure and sudden cardiac death. Molecular pathology Caused by defects of TNNI3, which encodes type-3 troponin I protein, TnI-cardiac (exclusively expressed in heart muscle).
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