| hemoglobinopathy | <disease, haematology> Disorder due to abnormalities in the haemoglobin molecule, the best known being sickle cell anaemia in which there is a single amino acid substitution (valine for glutamate) in position 6 of the beta chain. In other cases one of the globin chains is synthesised at a slower rate, despite being normal in structure. See: thalassaemia. Origin: Gr. Pathos = disease (18 Nov 1997) |
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| hemoglobinopathy |
a blood disease characterized by the presence of abnormal hemoglobins in the blood
Ãâó: wordnet.princeton.edu/perl/webwn
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| hemoglobinopathy |
Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. It is a collection of a number of diseases, including sickle cell anemia and thalassemia. ...
Ãâó: en.wikipedia.org/wiki/Hemoglobinopathy
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| hemoglobinopathy |
Category: Birth defects A blood disorder caused by alteration in the genetically determined molecular structure of hemoglobin (for example, sickle cell anemia). Find out more about Hemoglobinopathy: Articles | Books/products
Ãâó: pregnancyandbaby.com/read/articles/2447.htm
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| hemoglobinopathy |
( he-ma-glo-been-nop-a-the ): A term used to describe disorders caused by the presence of abnormal hemoglobin reproduction in the blood.
Ãâó: www.dhss.mo.gov/SickleCell/Glossary.html
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| hemoglobinopathy | a blood disease characterized by the presence of abnormal hemoglobins in the blood |
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