congenital disorder of glycosylation type IIb (DOID:0070254)
Alliance: disease page
Synonyms: CDG2B; CDG IIb; CDGIIb; glucosidase I deficiency
Alt IDs: OMIM:606056, MESH:C565264, ORDO:79330, UMLS_CUI:C1853736
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.