Congenital disorder of glycosylation type I
MONDO:0005500A 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.
Follow this condition — get notified about new trialsSub-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)