Hereditary persistence of fetal hemoglobin

The persistence of substantial fetal hemoglobin production into adulthood, usually associated with hemoglobinopathies due to mutations in the alpha and/or beta chain of hemoglobin.

Also known as: hereditary persistence of fetal hemoglobin, Disease, Haemoglobin F, Disease, Hemoglobin F, HEMOGLOBIN F DIS, HPFH - Hereditary persistence of fetal hemoglobin, HPFH - Hereditary persistence of foetal haemoglobin, Haemoglobin F Disease, Hb F disease

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