Delta-beta-thalassemia is a form of beta-thalassemia characterized by decreased or absent synthesis of the delta- and beta-globin chains with a compensatory increase in expression of fetal gamma-chain synthesis.
Comprehensive, easy-to-understand information about this condition
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beta-thalassemia-X-linked thrombocytopenia syndrome
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hemoglobin C-beta-thalassemia syndrome
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hemoglobin E-beta-thalassemia syndrome
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hemoglobin Lepore-beta-thalassemia syndrome
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hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
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beta thalassemia
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