- sickle cell–hemoglobin D disease
- a genetically determined anemia in which the erythrocytes contain both hemoglobin S and hemoglobin D, with symptoms like those of mild sickle cell anemia. Called also hemoglobin SD d.
Medical dictionary. 2011.
sickle cell–hemoglobin D disease
Look at other dictionaries:
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Sickle cell disease — A genetic blood disease due to the presence of an abnormal form of hemoglobin, namely hemoglobin S. Hemoglobin is the molecule in red blood cells that transports oxygen from the lungs to the farthest reaches of the body. Sickle cell disease, also … Medical dictionary
hemoglobin S–thalassemia — sickle cell–thalassemia disease … Medical dictionary
hemoglobinopathy — A disorder or disease caused by or associated with the presence of abnormal hemoglobins in the blood, e.g., sickle cell disease, hemoglobin C, D, E, H, or I disorders. Occasionally, combinations of abnormal hemoglobins are seen in… … Medical dictionary
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