About   Help   FAQ
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; Congenital disorder of glycosylation type IIg
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 COG1 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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.20
The Jackson Laboratory