All diseases

5 entries on 1 page. Showing entries 1 - 5.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00878 - Crigler-Najjar syndrome, type I 218800 0 0 UGT1A1 - -
01374 - Gilbert's syndrome 143500 0 0 UGT1A1 - -
02393 - Bilirubin, serum level of, quantitative trait locus 1 601816 0 0 UGT1A1 - -
02604 - Crigler-Najjar syndrome, type II 606785 1 0 UGT1A1 - -
01852 HBLRTFN hyperbilirubinemia, familial transient neonatal (Lucey-Driscoll syndrome (HBLRTFN)) 237900 0 0 UGT1A1 - -