Prader-Willi Syndrome is a genetic disorder characterized by several symptoms such as weak muscles, delayed development, intellectual disability, and excessive eating leading to obesity. Some of the synonyms for Prader-Willi Syndrome include Prader-Labhart-Willi Syndrome, Syndrome X, Hypothalamic Obesity, and Hyperphagic Obesity. These synonyms reflect the various aspects and effects of the disorder on an individual's physical and mental health. Although there is no cure for Prader-Willi Syndrome, early diagnosis and appropriate treatment can help manage the symptoms and improve quality of life. Further research and advancements in the medical field may lead to better understanding and treatment for this rare genetic disorder.