High affinity haemoglobin (Q39529): Difference between revisions

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+https://id.who.int/icd/entity/141481914
@@ Property / Canonical URI: https://id.who.int/icd/entity/141481914 / rank @@
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@@ Property / CURIE @@
+CID11:3A51.7
@@ Property / CURIE: CID11:3A51.7 / rank @@
+Normal rank
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+dki-india-3A51.7
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+Concluído
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+https://pauloleads.com.br/cases-publicos/
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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@@ Property / Collection date: 13 August 2026 / rank @@
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+D57
@@ Property / Linked ICD 10: D57 / rank @@
+Normal rank

Latest 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.