All diseases

OMIM ID
603585
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F
Alternative terms:

(∗) Location:
6q15  
(†) Associated OMIM genes:
SLC35A1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2jli9j6g