Hemoglobin C-Beta-Thalassemia Syndrome, also known as hbc-beta-thalassemia syndrome, is related to beta-thalassemia associated with another hemoglobin anomaly and beta-thalassemia. An important gene associated with Hemoglobin C-Beta-Thalassemia Syndrome is HBB (Hemoglobin Subunit Beta). Affiliated tissues include myeloid, and related phenotypes are splenomegaly and anemia