All diseases

OMIM ID
607091
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IId; CDG2D
Alternative terms:

(∗) Location:
9p21.1  
(†) Associated OMIM genes:
B4GALT1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2s8dtdyo