COG1-congenital disorder of glycosylation

MONDO:0012637

COG1-CDG is an extremely rare form of CDG syndrome characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation and facial dysmorphism.

Also known as: CDG syndrome type IIg, CDG-IIg, CDG2G, COG1-CDG, COG1-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type IIg, congenital disorder of glycosylation type 2g, congenital disorder of glycosylation type IIg

0 clinical trials for this condition and its sub-types, 0 tagged with COG1-congenital disorder of glycosylation itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic disease (7133) ↑ Cardiogenetic disease (614) ↑ Developmental anomaly of metabolic origin (383) ↑ Congenital disorder of glycosylation type II (3) ↑ Defect in conserved oligomeric Golgi complex (0)

Including sub-types (0) Tagged with COG1-congenital disorder of glycosylation (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.