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Sickle Cell Disease Ontology
Last uploaded:
May 6, 2021
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| Id | http://purl.obolibrary.org/obo/SCDO_0006905
http://purl.obolibrary.org/obo/SCDO_0006905
|
|---|---|
| Preferred Name | Hypersplenism |
| Definitions |
Condition characterized by splenomegaly, some reduction in the number of circulating blood cells in the presence of a normal or hyperactive bone marrow, and the potential for reversal by splenectomy.
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| Synonyms |
Hypersplenia
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | Condition characterized by splenomegaly, some reduction in the number of circulating blood cells in the presence of a normal or hyperactive bone marrow, and the potential for reversal by splenectomy. |
|---|---|
| skos:prefLabel | Hypersplenism
|
| rdfs:label | Hypersplenism
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| prefLabel | Hypersplenism
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| database cross reference | EFO:1000975
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| definition source | |
| prefixIRI | SCDO:0006905
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| previous identifier | SCDO:0006905
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| subClassOf | |
| type | |
| existence in other ontologies | Sufficient
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| hasExactSynonym | Hypersplenia
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| dc:source | Al-Salem, A. H. (2011). Splenic Complications of Sickle Cell Anemia and the Role of Splenectomy. ISRN Hematology, 2011, 864257. http://doi.org/10.5402/2011/864257
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| in guideline |
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