Disease - Cardiomyopathy, familial hypertrophic, 7
- DefinitionA hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
- AcronymCMH7
- Keywords
- Cross references
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Browse 1 entry- Troponin I, cardiac muscle · Gene: TNNI3 (TNNC1) · Homo sapiens (Human) · 210 amino acids · Evidence at protein level · Annotation score: 5/5