Statements (28)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
hemoglobin |
| gptkbp:alternativeName |
gptkb:HbSC_disease
gptkb:sickle-hemoglobin_C_disease |
| gptkbp:causedBy |
mutation in HBB gene
|
| gptkbp:complication |
gptkb:acute_chest_syndrome
stroke pulmonary embolism priapism |
| gptkbp:firstDescribed |
1940s
|
| gptkbp:gene |
gptkb:HbS/HbC
|
| https://www.w3.org/2000/01/rdf-schema#label |
hemoglobin SC disease
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:prevalence |
most common in people of African descent
|
| gptkbp:relatedTo |
gptkb:hemoglobin_C_disease
sickle cell disease |
| gptkbp:symptom |
gptkb:anemia
jaundice splenomegaly retinopathy avascular necrosis painful crises |
| gptkbp:treatment |
gptkb:hydroxyurea
pain management blood transfusion folic acid supplementation |
| gptkbp:bfsParent |
gptkb:Sickle_cell_disease
|
| gptkbp:bfsLayer |
6
|