Nonspherocytic hemolytic anemia
GPTKB entity
Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
gptkb:anemia |
| gptkbp:affects |
red blood cells
|
| gptkbp:cause |
gptkb:G6PD_deficiency
gptkb:hexokinase_deficiency pyruvate kinase deficiency |
| gptkbp:causedBy |
enzyme deficiency
hereditary condition |
| gptkbp:diagnosedBy |
enzyme assay
blood smear |
| https://www.w3.org/2000/01/rdf-schema#label |
Nonspherocytic hemolytic anemia
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:isNotCausedBy |
spherocyte formation
|
| gptkbp:subspecies |
congenital hemolytic anemia
|
| gptkbp:symptom |
gptkb:anemia
fatigue jaundice splenomegaly pallor |
| gptkbp:treatment |
gptkb:splenectomy
supportive care blood transfusion |
| gptkbp:bfsParent |
gptkb:P42127
gptkb:P32929 |
| gptkbp:bfsLayer |
7
|