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DOID:0070264 - congenital disorder of glycosylation type IIl
Disease Ontology 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.
Synonyms: CDG IIl, CDG syndrome type IIL, CDG2L, CDGIIdl, COG6-CGD, Congenital disorder of glycosylation type 2l,
Xenbase Genes : cog6
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee