Term Name:	congenital disorder of glycosylation type IIb
Synonyms:	CDG IIb, CDG2B, CDGIIb, glucosidase I deficiency
Definition:	A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the MOGS gene on chromosome 2p13.1.
Ontology:	Human Disease [DOID:0070254]   ( DOID:0070254 )