All diseases

OMIM ID
235555
OMIM term:
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2; CBAS2
Alternative terms:

(∗) Location:
7q33  
(†) Associated OMIM genes:
AKR1D1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/s4d0jj5b