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“hemoglobinopathies”
A blood disorder which is caused by a genetically determined change in the molecular structure of hemoglobin: Hemoglobinopathy is an ailment due to abnormalities in the hemoglobin molecule, the best known being "sickle cell anemia" in which there is a single amino acid substitution ("valine" for "glutamate") in position six of the beta chain. In other cases one of the globin chains is synthesised at a slower rate, despite being normal in structure.
This entry is located in the following units:
glob-, glom-
(page 5)
hem-, haem-, hemo-, haemo, hema-, haema-, hemato-, haemato-, hemat-, haemat-, -hemia, -haemia, -hemic, -haemic
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hemoglobin-, hemoglobino-, hemoglobini- +
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path-, patho-, -path-, -pathia, -pathic, -pathology, -pathetic, -pathize, -pathy
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