Human genes for congenital disorder of glycosylation type IIi
Congenital disorder of glycosylation type IIi [DOID:0070261]
A congenital disorder of glycosylation type II that has_material_basis_in a mutation of COG5 on chromosome 7q22.3.
Synonyms: congenital disorder of glycosylation type IIi, congenital disorder of glycosylation type IIis, DOID:0070261, Carbohydrate deficient glycoprotein syndrome type IIi, CDG2I ...