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Sickle Cell Anemia
A hereditary blood disorder characterized by abnormal hemoglobin, resulting in some red blood cells assuming an abnormal sickle shape.
B-Thalassemia Major
A severe blood disorder caused by a genetic mutation, leading to reduced production of hemoglobin and potentially severe anemia.
Hemophilia
A medical condition, usually inherited, in which the ability of the blood to clot is severely reduced, causing the sufferer to bleed severely from even a slight injury.
X-Linked Recessive
A pattern of genetic inheritance where the gene causing the trait or disorder is located on the X chromosome; more common in males who have only one X chromosome.
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