Hemoglobin Lepore-Beta-Thalassemia Syndrome, also known as hblepore-beta-thalassemia syndrome, is related to beta-thalassemia and thalassemia. An important gene associated with Hemoglobin Lepore-Beta-Thalassemia Syndrome is HBB (Hemoglobin Subunit Beta), and among its related pathways/superpathways is Golgi-to-ER retrograde transport.