- thalassemia–sickle cell disease
- sickle cell–thalassemia d.
Medical dictionary. 2011.
thalassemia–sickle cell disease
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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
