diagnosed using tool treated with has mode of inheritance has causal genotype has causal or contributing genetic variation has manifestation has causal molecular phenotype Severe Anemia Genetic Testing Blood Transfusion Electrophoresis Hemoglobin S Hemoglobin Profile Assay Sickle Cell Disease-S/O-Arab SO(Arab) disease http://newbornscreeningcodes.nlm.nih.gov/nb/sc/condition/Hb-F-S-O-Arab Hb F,S,O-Arab Sickle Cell-Hemoglobin O-Arab Disease Request inclusion into relevant ontology Sickle Cell-Haemoglobin O-Arab Disease Hb S O-Arab disease One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin O-Arab. It can cause anemia, repeated infections, and periodic episodes of pain and organ damage. Hemoglobin S O-Arab Disease Few but definitions not freely available Hb S,O-Arab Structural Hemoglobinopathy Hemoglobin O-Arab HBB, GLU6VAL HBB, GLU121LYS Hemoglobin Genotype S/O-Arab Compound Heterozygous Sickle Cell Disease Autosomal Recessive Compound Heterozygous