All diseases

OMIM ID
601110
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D
Alternative terms:
CDG Id; CDGId
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE IV, FORMERLY; CDGS4, FORMERLY
CDGS, TYPE IV, FORMERLY
(∗) Location:
3q27.1  
(†) Associated OMIM genes:
ALG3  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/15s9pw2g