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Sickle Cell Disease Ontology
Last uploaded:
May 6, 2021
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| Id | http://purl.obolibrary.org/obo/SCDO_0000343
http://purl.obolibrary.org/obo/SCDO_0000343
|
|---|---|
| Preferred Name | Delta Beta Thalassemia |
| Definitions |
A form of beta-thalassemia characterized by decreased or absent synthesis of the delta- and beta-globin chains with a compensatory increase in expression of fetal gamma-chain synthesis.
|
| Synonyms |
F Thalassaemia
Delta-Beta-Thalassaemia
Delta-Beta-Thalassemia
Delta Beta Thalassaemia
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A form of beta-thalassemia characterized by decreased or absent synthesis of the delta- and beta-globin chains with a compensatory increase in expression of fetal gamma-chain synthesis. |
|---|---|
| skos:prefLabel |
Delta Beta Thalassemia
|
| rdfs:label |
Delta Beta Thalassemia
|
| prefLabel |
Delta Beta Thalassemia
|
| database cross reference |
ORPHA:231237
|
| definition source | |
| prefixIRI |
SCDO:0000343
|
| previous identifier |
SCDO:0000343
|
| has causal genotype | |
| subClassOf | |
| has causal molecular phenotype | |
| type | |
| existence in other ontologies |
Sufficient
|
| has causal or contributing genetic variation | |
| hasExactSynonym |
F Thalassaemia
Delta-Beta-Thalassaemia
Delta-Beta-Thalassemia
Delta Beta Thalassaemia
|
| has mode of inheritance |
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