Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal
0.030 Biomarker disease BEFREE Inflammatory signature of cerebellar neurodegeneration during neonatal hyperbilirubinemia in Ugt1 <sup>-/-</sup> mouse model. 28340583 2017
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal
0.030 Biomarker disease BEFREE Modulation of bilirubin neurotoxicity by the Abcb1 transporter in the Ugt1-/- lethal mouse model of neonatal hyperbilirubinemia. 28025333 2017
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal
0.030 GeneticVariation disease BEFREE We studied mice in which the original Ugt1 locus was disrupted and replaced with the human UGT1 locus (hUGT1 mice); these mice spontaneously develop neonatal hyperbilirubinemia and BIND. 21983082 2012