EntityQ3616632· pop 14· linked from 203 articlesbeta thalassemiaSign in to savethalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobinConnectionssickle-cell diseaseEntityHemoglobin subunit betaEntityMediterranean SeaEntitygenetic diseaseEntityhematopoietic stem cellEntityzygosityEntityhereditary spherocytosisEntityfetal hemoglobinEntityhemoglobin CEntityTurkeyCountryEuropeEntityIndiaCountryGreeceCountryIranCountryPakistanCountryThailandCountryCambodiaCountryMaltaCountryCyprusCountryGreekEntityCategoriesDisorders of globin and globulin proteinsHereditary hemolytic anemiasRare diseasesSource attribution