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Congenital disorder of glycosylation type II

MONDO:0005501

A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain.

Also known as: congenital disorder of glycosylation type II, congenital disorders of glycosylation, type II, B4GALT1-CDG, B4GALT1-CDG (CDG-2d), MGAT2-CDG, MGAT2-CDG (CDG-2a), MOGS-CDG, MOGS-CDG (CDG-2b)

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

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Sub-types

Leukocyte adhesion deficiency type II (2) SLC35A2-congenital disorder of glycosylation (1) B4GALT1-congenital disorder of glycosylation (0) CCDC115-CDG (0) 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 2v (0) Congenital disorder of glycosylation, type IIaa (0) Congenital disorder of glycosylation, type IIbb (0) Congenital disorder of glycosylation, type IIcc (0) Congenital disorder of glycosylation, type IIq (0) Congenital disorder of glycosylation, type IIr (0) Congenital disorder of glycosylation, type iit (0) Congenital disorder of glycosylation, type IIw (0) Congenital disorder of glycosylation, type IIy (0) Congenital disorder of glycosylation, type IIz (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)
Trials to join now! 2 Not yet recruiting 1
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