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Disease Ontology Browser
congenital disorder of glycosylation type IIg (DOID:0070259)
Alliance: disease page
Synonyms: Carbohydrate deficient glycoprotein syndrome type IIg; CDG2G; CDG IIg; CDGII/COG1 cerebrocostomandibular-like syndrome; CDGIIg
Alt IDs: OMIM:611209, MESH:C535756, ORDO:263508, UMLS_CUI:C2931011
Definition: A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG1 gene on chromosome 17q25.1.

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