alpha-Thalassemia

Disease, Hemoglobin H; Diseases, Hemoglobin H; Hemoglobin H Diseases; Thalassemia alpha; Thalassemia-alphas; alpha Thalassemia; alpha-Thalassemias
A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.