Human genes for congenital disorder of glycosylation type IIg
Congenital disorder of glycosylation type IIg [DOID:0070259]
A congenital disorder of glycosylation type II that has_material_basis_in a mutation of COG1 on chromosome 17q25.1.
Synonyms: congenital disorder of glycosylation type IIg, congenital disorder of glycosylation type IIgs, DOID:0070259, Carbohydrate deficient glycoprotein syndrome type IIg, CDG2G ...