Hereditary persistence of fetal hemoglobin (HPFH) associated with beta-thalassemia is characterized by high hemoglobin (Hb) F levels and an increased number of fetal-Hb-containing-cells.
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beta-thalassemia-X-linked thrombocytopenia syndrome
MONDO:0010745
delta-beta-thalassemia
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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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beta thalassemia
MONDO:0019402