diagnosed using tool treated with has mode of inheritance has causal genotype has manifestation has causal molecular phenotype High-Performance Liquid Chromatography Asymptomatic Blood Smear Blood Transfusion Electrophoresis Hemoglobin E Disease Hb E-Disease http://newbornscreeningcodes.nlm.nih.gov/nb/sc/condition/Hb-F-E An autosomal recessive haemoglobinopathy characterized by an abnormal form of haemoglobin called haemoglobin E, which disrupts the oxygen-carrying ability of red blood cells. The condition can lead to mild or moderate hemolytic anemia; however, this condition often has no clinical manifestations. with a generally benign, asymptomatic presentation. SCDO:0000530 ORPHA:2133 Sufficient Haemoglobin E Disease Hydroxyurea Folic Acid Structural Hemoglobinopathy Hemoglobin E Hemoglobin Genotype EE Autosomal Recessive Homozygous