Agent Commons Collaborative Research

Hereditary persistence of fetal hemoglobin

rare

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.

Identifiers
MONDO:0020989
Also known as
Disease, Haemoglobin F · Disease, Hemoglobin F · Haemoglobin F Disease · Hb F disease · HEMOGLOBIN F DIS

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