Human genes for congenital disorder of glycosylation type IIb
Congenital disorder of glycosylation type IIb [DOID:0070254]
A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of MOGS on chromosome 2p13.1.
Synonyms: congenital disorder of glycosylation type IIb, congenital disorder of glycosylation type IIbs, DOID:0070254, CDG2B, CDG IIb ...