As shown in Table 1b, 15 conditions that are on the GHR list as having a genetic basis were observed on one or more state reportable conditions lists: Biotinidase Deficiency, Cancer, Congenital Anomalies, Congenital Hypothyroidism, Galactosemia, Guillain-Barre Syndrome, Hansen’s disease (Leprosy), Hemophilia, Kawasaki Syndrome, Lyme Disease, Maple Syrup Urine Disease, Phenylketonuria, Pulmonary Fibrosis, Sickle Cell Disease (newborns), and Transmissible Spongiform Encephalopathies (Prion Diseases). This evidence concerns the gene GHR and leprosy.