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Congenital disorder of glycosylation type I

MONDO:0005500

A congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor.

Also known as: congenital disorders of glycosylation, type I, ALG1-CDG, ALG1-CDG (CDG-1k), ALG11-CDG, ALG11-CDG (CDG-1p), ALG12-CDG, ALG12-CDG (CDG-1g), ALG2-CDG

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

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Sub-types

PMM2-congenital disorder of glycosylation (5) MPI-congenital disorder of glycosylation (1) PGM1-congenital disorder of glycosylation (1) ALG11-congenital disorder of glycosylation (0) ALG12-congenital disorder of glycosylation (0) ALG1-congenital disorder of glycosylation (0) ALG2-congenital disorder of glycosylation (0) ALG3-congenital disorder of glycosylation (0) ALG6-congenital disorder of glycosylation 1C (0) ALG8-congenital disorder of glycosylation (0) ALG9-congenital disorder of glycosylation (0) Congenital disorder of glycosylation type 1E (0) Congenital disorder of glycosylation, type IAA (0) Congenital disorder of glycosylation, type ICC (0) Congenital muscular dystrophy with intellectual disability and severe epilepsy (0) Congenital myasthenic syndrome 14 (0) DDOST-congenital disorder of glycosylation (0) Developmental and epileptic encephalopathy, 36 (0) Developmental and epileptic encephalopathy, 50 (0) DK1-congenital disorder of glycosylation (0)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Inborn errors of metabolism (42) Human disease (14) Congenital disorder of glycosylation (6) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0)
Trials to join now! 14 Not yet recruiting 4 Not yet finished but already full! 7 Completed 7 Terminated 1
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