Sickle Cell Disease Ontology Project

Mild Sickle Cell Disease-S Beta Minus Thalassemia

http://scdontology.h3abionet.org/ontology/SCDO_1000076

A form of sickle cell thalassemia, with a mild clinical phenotype, characterized by the presence of hemoglobin S and a small amount of hemoglobin A in the red blood cells.

Term info

curator note

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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

existence in other ontologies

None

Mild Sickle Cell-Beta Minus Thalassemia, Mild Sickle Cell-Beta Minus Thalassaemia, Mild Sickle Cell Disease-S Beta Minus Thalassaemia

Term relations

Subclass of:

Sickle Cell Disease-S Beta Minus Thalassemia