All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02393 BILIQTL1 bilirubin, serum level of, quantitative trait locus, type 1 601816 - - - UGT1A1 - -
05811 Crigler-Najjar Crigler-Najjar syndrome - AR 175 173 UGT1A1 - -
00878 Crigler-Najjar I Crigler-Najjar syndrome, type I 218800 AR 8 1 UGT1A1 - -
02604 Crigler-Najjar II Crigler-Najjar syndrome, type II 606785 AR 8 - UGT1A1 - -
01374 Gilbert syndrome Gilbert syndrome 143500 AR 92 58 UGT1A1 - -
01852 HBLRTFN hyperbilirubinemia, familial transient neonatal (Lucey-Driscoll syndrome (HBLRTFN)) 237900 AR - - UGT1A1 - -
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