Hereditary persistence of fetal haemoglobin (Q39520)

From determinar.ia.br - Determine suas informações
Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia.
Language Label Description Also known as
default for all languages
3A50.4
    English
    Hereditary persistence of fetal haemoglobin
    Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia.

      Statements

      CID11:3A50.4
      0 references
      dki-india-3A50.4
      0 references
      Concluído
      0 references
      13 August 2026
      0 references
      0 references