Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
hemoglobin |
| gptkbp:affects |
red blood cells
|
| gptkbp:causedBy |
inheritance of one hemoglobin S gene and one hemoglobin C gene
|
| gptkbp:complication |
gptkb:acute_chest_syndrome
stroke avascular necrosis retinal disease |
| gptkbp:diagnosedBy |
hemoglobin electrophoresis
|
| https://www.w3.org/2000/01/rdf-schema#label |
HbSC disease
|
| gptkbp:ICD-10_code |
gptkb:D57.0
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:OMIM |
603903
|
| gptkbp:prevalence |
most common in people of African descent
|
| gptkbp:relatedTo |
gptkb:hemoglobin_C_disease
sickle cell disease |
| gptkbp:symptom |
gptkb:anemia
splenomegaly retinopathy painful crises mild hemolysis |
| gptkbp:treatment |
gptkb:hydroxyurea
pain management blood transfusion |
| gptkbp:bfsParent |
gptkb:hemoglobin_SC_disease
|
| gptkbp:bfsLayer |
7
|