Human genes for congenital disorder of glycosylation type IIf
Congenital disorder of glycosylation type IIf [DOID:0070258]
A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of SLC35A1 on chromosome 6q15.
Synonyms: congenital disorder of glycosylation type IIf, congenital disorder of glycosylation type IIfs, DOID:0070258, Carbohydrate deficient glycoprotein syndrome type IIf, CDG2F ...