eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | congenital nonhemolytic jaundice |
| Comorbidity | C0017920|g6pd deficiency |
| Sentences | 2 |
| PubMedID- 22407023 | The results showed that in certain cases, the presence of hyperbilirubinemia is not only associated with g6pd deficiency, but may be caused by the co-presence of a mutation in the ugta1 promoter related to gilbert's syndrome. |
| PubMedID- 22906047 | There is significant association of g6pd deficiency with neonatal hyperbilirubinemia in the immediate perinatal period [3]. |
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