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STO
Last uploaded:
November 28, 2017
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| Id | http://www.semanticweb.org/ontologies/STO.owl#OWLClass_25e9091d_53fa_41d8_b73c_b38336bcf857
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_25e9091d_53fa_41d8_b73c_b38336bcf857
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|---|---|
| Preferred Name | Sickle cell disease |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
Sickle cell disease
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|---|---|
| prefLabel |
Sickle cell disease
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| hasDbXref |
MIM: 603903
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| synonyms |
SCD
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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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| isDefinedBy |
Sickle-cell disease is one of the most important hemoglobinopathies and the most prevalent form of congenital hemolytic anemia.
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| prefixIRI |
OWLClass_25e9091d_53fa_41d8_b73c_b38336bcf857
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| subClassOf | |
| type | |
| source |
Merritt, H. H. (2010). Merritt's neurology. L. P. Rowland, & T. A. Pedley (Eds.). Lippincott Williams & Wilkins.
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