Congenital Disorder

Thalassemia

AMW:DIS:150022

A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.

Pathology clinical

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Thalassemia has parent Anemia, Hemolytic, Congenital

Thalassemia has parent Hemoglobinopathies

alpha-Thalassemia has parent Thalassemia

beta-Thalassemia has parent Thalassemia

delta-Thalassemia has parent Thalassemia

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