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DOID:0070254 - congenital disorder of glycosylation type IIb
Disease Ontology 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.
Synonyms: CDG IIb, CDG2B, CDGIIb, glucosidase I deficiency,
Xenbase Genes : mogs
MONDO:0011629 - MOGS-congenital disorder of glycosylation |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee