A heterozygous state in which a person has a hemoglobin S allele along with a beta-thalassemia allele. The severity of the condition is determined to a large extent by the quantity of normal hemoglobin produced by the beta-thalassemia gene.
NCIT:C95539
http://bioportal.bioontology.org/ontologies/NCIT?p=classes&conceptid=http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C61237
Sufficient
Sickle Cell-Beta-Thalassemia Disease Syndrome, Sickle Cell-Beta Thalassaemia, Sickle Beta-Thalassaemia, Sickle Cell-Beta-Thalassemia, S-Beta Thalassemia, Sickle Beta Thalassaemia, Sickle Cell Beta Thalassemia Disease, HbS-Beta-Thalassemia Syndrome, HbSBetaThal, Sickle Cell Disease-S Beta Thalassaemia, S Beta-Thalassemia, Hb S-Beta Thalassemia
