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Sickle Cell Disease Ontology
Last uploaded:
May 6, 2021
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| Id | http://purl.obolibrary.org/obo/SCDO_0000552
http://purl.obolibrary.org/obo/SCDO_0000552
|
|---|---|
| Preferred Name | Hemoglobinopathy |
| Definitions |
An inherited disorder of the structure and/or synthesis of hemoglobin, with a variable phenotype expression ranging from benign to severe.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | An inherited disorder of the structure and/or synthesis of hemoglobin, with a variable phenotype expression ranging from benign to severe. |
|---|---|
| skos:prefLabel |
Hemoglobinopathy
|
| rdfs:label |
Hemoglobinopathy
|
| prefLabel |
Hemoglobinopathy
|
| database cross reference |
NCIT:C3092
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| definition source | |
| prefixIRI |
SCDO:0000552
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| subClassOf | |
| curator note |
Suggest update to description in NCIT
|
| type | |
| existence in other ontologies |
Suggest update to description
|
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