Congenital Hemolytic Spherocytic Syndrome
GPTKB entity
Statements (20)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
hereditary hemolytic anemia |
| gptkbp:affects |
red blood cells
|
| gptkbp:alsoKnownAs |
gptkb:Hereditary_Spherocytosis
|
| gptkbp:causedBy |
defect in red blood cell membrane proteins
|
| gptkbp:complication |
gptkb:aplastic_crisis
gallstones |
| gptkbp:diagnosedBy |
gptkb:osmotic_fragility_test
blood smear |
| gptkbp:hasEpidemiology |
most common inherited hemolytic anemia in people of Northern European descent
|
| gptkbp:hasGeneticInheritance |
autosomal dominant
autosomal recessive |
| https://www.w3.org/2000/01/rdf-schema#label |
Congenital Hemolytic Spherocytic Syndrome
|
| gptkbp:symptom |
gptkb:anemia
jaundice splenomegaly |
| gptkbp:treatment |
gptkb:splenectomy
folic acid supplementation |
| gptkbp:bfsParent |
gptkb:CHSS
|
| gptkbp:bfsLayer |
7
|