DISEASES

Disease-gene associations mined from literature

Human genes for congenital disorder of glycosylation type IIl

Congenital disorder of glycosylation type IIl [DOID:0070264]

A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of COG6 on chromosome 13q14.11.

Synonyms:  congenital disorder of glycosylation type IIl,  DOID:0070264,  congenital disorder of glycosylation type IIls,  CDG IIl,  CDG syndrome type IIL ...