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Delta Beta-Thalassemia

Disease ID: disease_node_15243

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DbxrefNCI:C172823, ORDO:231237
SubclassofDOID_0050736, DOID_12241
Data SourceDOID
Doid Labeldelta beta-thalassemia
Doid DescriptionA beta thalassemia that is characterized by decreased or absent synthesis of both the delta- and beta-globin chains, which leads to a compensatory increase in fetal gamma-chain synthesis. This disorder results in a microcytic anemia that is clinically mild.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_15243
Doid IdDOID_0080773
LabelDelta Beta-Thalassemia