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disease > genetic disease > hereditary disease > thalassemia > β-thalassemia

... > hemopathy > anemia > hemolytic anemia > thalassemia > β-thalassemia

disease > hemopathy > hemoglobinopathy > thalassemia > β-thalassemia

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β-thalassemia

Definición

Beta thalassemias (β thalassemias) are a group of inherited blood disorders. They are forms of thalassemia caused by reduced or absent synthesis of the beta chains of hemoglobin that result in variable outcomes ranging from severe anemia to clinically asymptomatic individuals. (Wikipedia)

Concepto genérico

thalassemia

Conceptos específicos

hereditary persistence of fetal hemoglobin

En otras lenguas

thalassémie β

francés

URI

http://data.loterre.fr/ark:/67375/VH8-PFM79XR5-6

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