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Beta thalassemia
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Hereditary blood disorder causing anemia
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Wikipedia

Beta-thalassemia (β-thalassemia) is an inherited blood disorder, a form of thalassemia resulting in variable outcomes ranging from clinically asymptomatic to severe anemia individuals. It is caused by reduced or absent synthesis of the beta chains of hemoglobin, the molecule that carries oxygen in the blood. Symptoms depend on the extent to...

Instance of
Rare disease
class of disease
Subclass of
Thalassemia
Disease
References
Wikidata