Hereditary persistence of fetal haemoglobin - sickle cell disease (Q59821): Difference between revisions

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Latest revision as of 07:20, 14 August 2026

This is a benign condition in which significant fetal haemoglobin (haemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult-type haemoglobin should be produced. This diagnosis is with sickle cell disease.

Language	Label	Description	Also known as
default for all languages	ID_1455152722
English	Hereditary persistence of fetal haemoglobin - sickle cell disease	This is a benign condition in which significant fetal haemoglobin (haemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult-type haemoglobin should be produced. This diagnosis is with sickle cell disease.