Sickle Cell-Hemoglobin C Disease Syndrome, also known as sickle cell-hemoglobin c disease, is related to hemoglobin c disease and thalassemia. An important gene associated with Sickle Cell-Hemoglobin C Disease Syndrome is HBB (Hemoglobin Subunit Beta). The drugs Fludarabine and Cytarabine have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and bone.