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disease > genetic disease > hereditary disease > thalassemia > α-thalassemia
... > disease > hemopathy > anemia > hemolytic anemia > thalassemia > α-thalassemia
disease > hemopathy > hemoglobinopathy > thalassemia > α-thalassemia

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α-thalassemia  

Definición

  • Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of alpha chains from 1, 2, 3, or all 4 of the alpha globin genes, leading to a relative excess of beta globin chains. (Wikipedia)

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http://data.loterre.fr/ark:/67375/VH8-GZD85Q46-F

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