A variant of sickle cell disease due to heterozygosity for hemoglobin S and hemoglobin D mutations. Patients present with the symptoms of sickle cell disease but the symptoms are less frequent and severe compared to patients with hemoglobin SS disease.
NCIT:C155310
http://bioportal.bioontology.org/ontologies/NCIT?p=classes&conceptid=http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C155310
Sufficient
Sickle Cell-Hemoglobin D Disease, Sickle Cell Hemoglobin D Disease, Hemoglobin Sickle D Disease, Hemoglobin S-D Disease, Hb SD-Disease, Sickle Cell-Haemoglobin D Disease, Haemoglobin S-D Disease, Sickle Cell Disease SD
