PGT-M is a shortcut of Preimplantation Genetic Testing for Monogenic Diseases or previously known as Preimplantation Genetic Diagnosis (PGD). PGT-M makes it possible for a couple with hereditary genetics within their family to avoid passing it on to their children. This is a test that is conducted before implementation to help identify abnormalities in a single gene of embryo when IVF to avoid genetic pregnancy with an abnormality. Preparation that is conducted before starting PGT-M siclus through genetic counseling. When doing PGT-M might be required to take samples from a couple and family directed as a reference. All of the tests should be scheduled at first and coordinated through Diagnos Genomics.