DISEASES

Disease-gene associations mined from literature

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,  DOID:0070261,  congenital disorder of glycosylation type IIis,  CDG IIi,  CDG syndrome type IIi ...