Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
hemoglobin |
| gptkbp:affects |
hemoglobin
|
| gptkbp:alsoKnownAs |
HbC disease
Hemoglobin C anemia |
| gptkbp:causedBy |
mutation in HBB gene
|
| gptkbp:complication |
gallstones
splenic sequestration |
| gptkbp:diagnosedBy |
hemoglobin electrophoresis
|
| gptkbp:firstDescribed |
1950
|
| https://www.w3.org/2000/01/rdf-schema#label |
Hemoglobin C Disease
|
| gptkbp:ICD-10_code |
D58.2
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:OMIM |
603903
|
| gptkbp:prevalence |
gptkb:African-American
gptkb:West_Africa |
| gptkbp:symptom |
jaundice
splenomegaly mild hemolytic anemia |
| gptkbp:treatment |
supportive care
folic acid supplementation |
| gptkbp:bfsParent |
gptkb:Target_Cells
|
| gptkbp:bfsLayer |
8
|