Preferred Name | Thalassemia | |
Synonyms |
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ID |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_181e30a5_7bc0_47d3_8d93_5b1a99889f92 |
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hasDbXref | ||
isDefinedBy |
Thalassemia is a congenital hemolytic disorder primarily found in individuals of Mediterranean descent. It is caused by a partial or complete deficiency in the synthesis of hemoglobin subunits. |
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label |
Thalassemia |
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prefixIRI |
OWLClass_181e30a5_7bc0_47d3_8d93_5b1a99889f92 |
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prefLabel |
Thalassemia |
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references |
Robert Bühler, Heinrich P. Mattle, Chapter 45 Hematological diseases and stroke, Handbook of Clinical Neurology, Elsevier, 2008, Volume 93, Pages 887-934 Cohen AR, Galanello R, Pennell DJ, et al. (2004). Thalassemia. Hematology Am Soc Hematol Educ Program 14–34 |
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synonyms |
Hereditary leptocytosis |
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subClassOf |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_343b79ba_eb5f_48f6_9429_1dd27e96eb72 |
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