High affinity haemoglobin (Q39529): Difference between revisions

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Doença causada por determinantes que surgem após o nascimento, no período pré-natal, ou por fatores geneticamente herdados, levando à formação de hemoglobina com alta afinidade pelo oxigênio. Essa doença é caracterizada por anormalidades das cadeias de globina que alteram a afinidade da molécula de hemoglobina pelo oxigênio, prejudicando o carregamento normal de oxigênio nos pulmões e a oferta de oxigênio aos tecidos.
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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.

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.
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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.

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