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congenital disorder of glycosylation type II (DOID:0050571)
Alliance: disease page
Synonyms: B4GALT1-CDG (CDG-2d); MGAT2-CDG (CDG-2a); MOGS-CDG (CDG-2b)
Alt IDs: OMIM:212066, OMIM:266265, OMIM:300896, OMIM:603585, OMIM:606056, OMIM:607091, OMIM:608779, OMIM:611182, OMIM:611209, OMIM:613489, OMIM:613612, OMIM:614576, OMIM:614727
Definition: A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.12
The Jackson Laboratory