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.