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Defect in conserved oligomeric Golgi complex

MONDO:0017750

Also known as: defect in COG complex

0 clinical trials for this condition and its sub-types.

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Sub-types

COG1-congenital disorder of glycosylation (0) COG4-congenital disorder of glycosylation (0) COG5-congenital disorder of glycosylation (0) COG6-congenital disorder of glycosylation (0) COG7-congenital disorder of glycosylation (0) COG8-congenital disorder of glycosylation (0) Congenital disorder of glycosylation, type IIq (0)

Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Congenital disorder of glycosylation (7) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of multiple glycosylation (0)

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