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Disease Ontology Browser
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 MOGS on chromosome 2p13.1.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory