All diseases

OMIM ID
608799
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie; CDG1E
Alternative terms:

(∗) Location:
20q13.13  
(†) Associated OMIM genes:
DPM1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/0wajm9j5