Severe Sickle Cell Disease-S Beta Minus Thalassemia
A form of sickle cell thalassemia, with a severe clinical phenotype, characterized by the presence of hemoglobin S and a small amount of hemoglobin A in the red blood cells.
Sickle Cell Disease Ontology Project
Term info
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dc:creator
SCDO (Clair Ingram)
definition source
Rees, D.C., Williams, T.N. and Gladwin, M.T., 2010. Sickle-cell disease. The Lancet, 376(9757), pp.2018-2031., http://bioportal.bioontology.org/ontologies/NCIT/?p=classes&conceptid=http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C98837
Severe Sickle Cell Disease-S Beta Minus Thalassaemia, Severe Sickle Cell-Beta Minus Thalassaemia, Severe Sickle Cell-Beta Minus Thalassemia
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