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Summary Literature (0)
MIM:602579 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B

Xenbase Genes: mpi

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011257 - MPI-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080554 - congenital disorder of glycosylation Ib