Agent Commons Collaborative Research

Defect in conserved oligomeric Golgi complex

rare
Identifiers
MONDO:0017750 Orphanet:309568
Part of
Disorder of multiple glycosylation
Also known as
defect in COG complex

Subtypes

All diseases Rare only
Disease Subtypes
COG1-congenital disorder of glycosylation
COG4-congenital disorder of glycosylation
COG5-congenital disorder of glycosylation
COG6-congenital disorder of glycosylation
COG7-congenital disorder of glycosylation
COG8-congenital disorder of glycosylation
Congenital disorder of glycosylation, type IIq

Rare disease

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