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DOID:5212 - congenital disorder of glycosylation
Disease Ontology Definition:A carbohydrate metabolic disorder that involves deficient or defective glycosylation of a variety of tissue proteins and/or lipids.
Synonyms: carbohydrate-deficient glycoprotein syndrome,
Xenbase Genes : alg2, cog6, pgm1, cog5, atp6ap1, dpagt1, cog8, cog2, dolk, alg8, ssr4, stt3b, cog7, tmem165, mpi,
MONDO:0015286 - congenital disorder of glycosylation |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee