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

22 clinical trials for this condition and its sub-types, 0 tagged with Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Beta-thalassemia and related diseases (99)

Including sub-types (22) Tagged with Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.