diagnosed using tool has manifestation Jaundice Cholelithiasis Cardiomegaly Splenomegaly Anemia Hyperuricemia Genetic Testing Iron Overload Blood Smear Beta Thalassemia Intermedia SCDO:0000112 A homozygous (B+/B+) or compound heterozygous (B0/B+) form of beta-thalassemia characterized by mild to moderate anemia which does not or only occasionally requires transfusion. Sufficient Thalassemia Intermedia Beta-Thalassemia Intermedia B0/B+ B+/B+ ORPHA:231222 Clinical Phenotype of Beta Thalassemia Hemoglobin Profile Assay Leg Ulcer Hypersplenism