Our approach is to find a solution to cure many rare diseases using novel big data, deep learning, genome analysis and mRNA structures.Our focus lies with a gene inefficiency to produce specific protein, resulting in a unique genetic disorder. We're coping with these disorders by implementing a technological platform based on the messenger RNA directed at bringing innovative therapies for inherited or acquired diseases. The idea of mRNA as a therapeutic mechanism created an opportunity for addressing previously unmet clinical needs, especially considering the vast area of rare diseases.