All diseases

OMIM ID
608540
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K
Alternative terms:

(∗) Location:
16p13.3  
(†) Associated OMIM genes:
ALG1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/mbrcfg0z