Establishes central registry for sickle cell trait diagnoses; provides for informational outreach and genetic counseling.

This bill (S 3322) requires New Jersey to create a central registry for newborns diagnosed with sickle cell trait - a genetic condition where a person carries one sickle cell gene but typically does not have sickle cell disease. It mandates that newborn screening labs notify physicians, who must then provide parents with information about genetic counseling. The registry will track cases to ensure parents receive timely notifications during early adolescence (for athletic safety) and later adolescence (for reproductive planning), while keeping all health data confidential. The bill directly affects newborns with sickle cell trait and their families in New Jersey.