COG5-congenital disorder of glycosylation

MONDO:0013325

COG5-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case to date by moderate mental retardation with slow and inarticulate speech, truncal ataxia, and mild hypotonia.

Also known as: CDG syndrome type III, CDG-III, CDG2I, COG5-CDG, COG5-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type III, congenital disorder of glycosylation type 2i, congenital disorder of glycosylation type III

0 clinical trials for this condition and its sub-types, 0 tagged with COG5-congenital disorder of glycosylation itself.

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↑ Syndromic disease (7158) ↑ Congenital disorder of glycosylation type II (3) ↑ Defect in conserved oligomeric Golgi complex (0)

Including sub-types (0) Tagged with COG5-congenital disorder of glycosylation (0)

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