All diseases

OMIM ID
608093
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J
Alternative terms:

(∗) Location:
11q23.3  
(†) Associated OMIM genes:
DPAGT1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/vf3x88e4