loading...| Preferred Name | Sickle cell disease | |
| Synonyms |
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| ID |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_25e9091d_53fa_41d8_b73c_b38336bcf857 |
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| hasDbXref |
MIM: 603903 |
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| isDefinedBy |
Sickle-cell disease is one of the most important hemoglobinopathies and the most prevalent form of congenital hemolytic anemia. |
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| label |
Sickle cell disease |
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| prefixIRI |
OWLClass_25e9091d_53fa_41d8_b73c_b38336bcf857 |
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| prefLabel |
Sickle cell disease |
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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 Serjeant, G. R. (1997). Sickle-cell disease. The Lancet, 350(9079), 725-730. |
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| source |
Merritt, H. H. (2010). Merritt's neurology. L. P. Rowland, & T. A. Pedley (Eds.). Lippincott Williams & Wilkins. |
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| synonyms |
SCD |
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| subClassOf |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_a870b44b_eab9_424a_8edb_c063407aeefc http://www.semanticweb.org/ontologies/STO.owl#OWLClass_75f16a76_83e5_4163_bebb_a6dd64fdb892 |