All diseases

OMIM ID
610768
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M
Alternative terms:
CDG Im; CDGIm
DOLICHOL KINASE DEFICIENCY
DK1 DEFICIENCY
(∗) Location:
9q34.11  
(†) Associated OMIM genes:
DOLK  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/xl78i4ru