- OMIM ID
-
603147
- OMIM term:
- CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C
- Alternative terms:
-
CDG Ic; CDGIc
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I, WITH DEFICIENT GLYCOSYLATION OF DOLICHOL-LINKED OLIGOSACCHARIDE, FORMERLY
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE V, FORMERLY; CDGS5, FORMERLY
- (∗) Location:
- 1p31.3
- (†) Associated OMIM genes:
- ALG6
- (‡) Associated MGI genes:
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