Statements (27)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb:hemoglobin |
| gptkbp:causedBy |
mutation in HBB gene
|
| gptkbp:complication |
gptkb:acute_chest_syndrome
stroke infections leg ulcers |
| gptkbp:diagnosedBy |
genetic testing
hemoglobin electrophoresis |
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:OMIM |
603902
|
| gptkbp:prevalence |
gptkb:Mediterranean_populations
gptkb:Middle_Eastern_populations Indian populations |
| gptkbp:relatedTo |
gptkb:beta-thalassemia
sickle cell disease |
| gptkbp:symptom |
gptkb:anemia
jaundice splenomegaly growth retardation painful crises |
| gptkbp:treatment |
gptkb:hydroxyurea
blood transfusions bone marrow transplant |
| gptkbp:bfsParent |
gptkb:Sickle_cell_disease
|
| gptkbp:bfsLayer |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
sickle beta-thalassemia
|