congenital disorder of glycosylation type II Disease Ontology Browser

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Disease Ontology Browser

congenital disorder of glycosylation type II (DOID:0050571)
Alliance: disease page
Alt IDs: MESH:C535747, OMIM:PS212066
Definition: A congenital disorder of glycosylation that involves malfunctioning trimming or processing of the protein-bound oligosaccharide chain.

Disease References using Mouse Models (2)

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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