eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | congenital nonhemolytic jaundice |
| Symptom | C0020433|hyperbilirubinemia |
| Sentences | 5 |
| PubMedID- 24636296 | Objective: to explore the pathological characteristics of inborn hyperbilirubinemia of patients with gilbert's syndrome (gs). |
| PubMedID- 22360405 | gilbert's syndrome--a frequent cause of unconjugated hyperbilirubinemia in children after orthotopic liver transplantation. |
| PubMedID- 24615032 | gilbert's syndrome is suspected in patients with unconjugated hyperbilirubinemia caused by decreased activity of the udp-glucuronosyltransferase 1a1 (ugt1a1) gene in the absence of abnormal liver function and hemolysis. |
| PubMedID- 20389299 | Pazopanib-induced hyperbilirubinemia is associated with gilbert's syndrome ugt1a1 polymorphism. |
| PubMedID- 23689708 | Zinc sulfate (znso4) reduces unconjugated hyperbilirubinemia in individuals with gilbert's syndrome. |
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