- OMIM ID
-
602579
- OMIM term:
- CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B
- Alternative terms:
-
CDG Ib; CDGIb
CDG, GASTROINTESTINAL TYPE
MANNOSEPHOSPHATE ISOMERASE DEFICIENCY
MPI DEFICIENCY
PROTEIN-LOSING ENTEROPATHY-HEPATIC FIBROSIS SYNDROME
SAGUENAY-LAC SAINT-JEAN SYNDROME; SLSJ SYNDROME
- (∗) Location:
- 15q24.1
- (†) Associated OMIM genes:
- MPI
- (‡) Associated MGI genes:
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