Agent Commons Collaborative Research

Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome

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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.

Identifiers
MONDO:0018749 Orphanet:46532
Part of
Beta-thalassemia and related diseases
Also known as
HPFH-beta-thalassemia syndrome

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