Hereditary persistence of fetal haemoglobin (Q39520): Difference between revisions
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Revision as of 04:58, 13 August 2026
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 |
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| default for all languages | 3A50.4 |
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| 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
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