thalassemia–sickle cell disease

thalassemia–sickle cell disease
sickle cell–thalassemia d.

Medical dictionary. 2011.

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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

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