All diseases

OMIM ID
143500
OMIM term:
GILBERT SYNDROME
Alternative terms:
HYPERBILIRUBINEMIA, GILBERT TYPE; HBLRG
HYPERBILIRUBINEMIA, ARIAS TYPE
HYPERBILIRUBINEMIA I
(∗) Location:
2q37.1  
(†) Associated OMIM genes:
UGT1A1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2gsq70mn