Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:affects |
hemoglobin
|
| gptkbp:alsoKnownAs |
HbC disease
|
| 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:inheritance |
autosomal recessive
|
| gptkbp:prevalence |
most common in people of West African descent
|
| gptkbp:relatedTo |
gptkb:hemoglobin_SC_disease
sickle cell disease |
| gptkbp:symptom |
jaundice
splenomegaly mild hemolytic anemia |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:hemoglobin_C
|
| gptkbp:bfsLayer |
6
|