High affinity haemoglobin (Q39529): Difference between revisions
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Revision as of 04:58, 13 August 2026
A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormalities in the globin chains that alter the affinity of the haemoglobin molecule for oxygen, affecting the normal loading of oxygen in the lungs and delivery of oxygen to the tissues.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A51.7 |
||
| English | High affinity haemoglobin |
A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormalities in the globin chains that alter the affinity of the haemoglobin molecule for oxygen, affecting the normal loading of oxygen in the lungs and delivery of oxygen to the tissues. |
Statements
CID11:3A51.7
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dki-india-3A51.7
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Concluído
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