Term Name:	congenital disorder of glycosylation type IIl
Synonyms:	CDG IIl, CDG syndrome type IIL, CDG2L, CDGIIl, COG6-CGD, Congenital disorder of glycosylation type 2l
Definition:	A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the COG6 gene on chromosome 13q14.11.
Ontology:	Human Disease [DOID:0070264]   ( DOID:0070264 )