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
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/19/2024
MGI 6.24
The Jackson Laboratory