diagnosed using tool has mode of inheritance has causal genotype has causal or contributing genetic variation has manifestation has causal molecular phenotype Acute Chest Syndrome Cholelithiasis Splenomegaly Anemia Osteonecrosis Genetic Testing Osteonecrosis of the Femoral Head Electrophoresis Hematuria Hemoglobin S Pain Sickle Cell Disease-SE Suggest update to description of "Sickle Cell-Hemoglobin D Disease" in the NCIT. Hb SE-Disease Sickle Cell-Haemoglobin E Disease http://newbornscreeningcodes.nlm.nih.gov/nb/sc/condition/Hb-F-S-E Hemoglobin SE Disease Few but definitions not specific enough Hemoglobin SE-Disease Sickle Cell-Hemoglobin E Disease A variant of sickle cell disease due to heterozygosity for hemoglobin S and hemoglobin E mutations, which can cause mild hemolytic anemia. Sickle Cell Disease SE Sickle Retinopathy Splenic Infarction Structural Hemoglobinopathy Splenic Sequestration Hemoglobin E HBB, GLU6VAL HBB, GLU26LYS Hemoglobin Genotype SE Compound Heterozygous Sickle Cell Disease Autosomal Recessive Compound Heterozygous