Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome

MONDO:0018749

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.

Also known as: HPFH-beta-thalassemia syndrome

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