All diseases

OMIM ID
607765
OMIM term:
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1
Alternative terms:

(∗) Location:
16p11.2  
(†) Associated OMIM genes:
HSD3B7  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/clfia894