Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome

Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome, also known as hpfh-beta-thalassemia syndrome, is related to neonatal anemia and anemia, congenital dyserythropoietic, type iv. An important gene associated with Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome is HBB (Hemoglobin Subunit Beta), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Golgi-to-ER retrograde transport. Affiliated tissues include bone, and related phenotypes are splenomegaly and anemia