All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

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 - -
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