All diseases

OMIM ID
218800
OMIM term:
CRIGLER-NAJJAR SYNDROME, TYPE I
Alternative terms:
HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE I; HBLRCN1
CRIGLER-NAJJAR SYNDROME
(∗) Location:
2q37.1  
(†) Associated OMIM genes:
UGT1A1  
(‡) Associated MGI genes:
Ugt1  

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