Alpha thalassaemia myelodysplastic syndrome (Q91736): Difference between revisions

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Latest revision as of 18:46, 15 August 2026

Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells.

Language	Label	Description	Also known as
default for all languages	ID_1991581630
English	Alpha thalassaemia myelodysplastic syndrome	Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells.