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.

Look at other dictionaries:

  • sickle cell–hemoglobin C disease — a genetically determined anemia in which the erythrocytes contain both hemoglobin S and hemoglobin C; symptoms are similar to but less severe than those of sickle cell anemia and may include abdominal and skeletal pain, splenomegaly, splenic… …   Medical dictionary

  • hemoglobin SC disease — sickle cell–hemoglobin C d …   Medical dictionary

  • hemoglobin SD disease — sickle cell–hemoglobin D d …   Medical dictionary

  • sickle cell–thalassemia disease — any of several hereditary anemias involving simultaneous heterozygosity for hemoglobin S and a thalassemia gene; symptoms resemble those of sickle cell anemia. Called also microdrepanocytosis, microdrepanocytic d., hemoglobin S–thalassemia,… …   Medical dictionary

  • 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

  • Cell — The basic structural and functional unit in people and all living things. Each cell is a small container of chemicals and water wrapped in a membrane. Each cell in the human body there are 100 trillion cells in each of us contains the entire… …   Medical dictionary

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