Cardiac genetic disorders constitute a distinctive category of genetic anomalies affecting the heart's structure and function. These disorders encompass a spectrum of variations in the genes responsible for cardiovascular health, influencing aspects such as heart development, rhythm, and overall functionality. Some of these genetic conditions may heighten the susceptibility to congenital heart defects, while others can increase the risk of developing arrhythmias or cardiomyopathies. Unraveling the genetic underpinnings of cardiac disorders holds paramount importance, providing insights for early detection, risk evaluation, and the formulation of personalized treatment plans. Ongoing advancements in genetic testing and research contribute to a deeper comprehension of the complex interplay between genetics and cardiac well-being. This evolving understanding opens avenues for enhanced interventions and individualized strategies aimed at managing and alleviating the impact of cardiac genetic disorders.