COG8-congenital disorder of glycosylation

MONDO:0012635

The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type IIh is characterized by severe psychomotor retardation, failure to thrive and intolerance to wheat and dairy products.

Also known as: CDG syndrome type IIh, CDG-IIh, CDG2H, COG8-CDG, COG8-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type IIh, congenital disorder of glycosylation type 2h, congenital disorder of glycosylation type IIh

0 clinical trials for this condition and its sub-types, 0 tagged with COG8-congenital disorder of glycosylation itself.

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

Including sub-types (0) Tagged with COG8-congenital disorder of glycosylation (0)

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