Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Congenital disorder of glycosylation

ALG14-congenital disorder of glycosylation

Deficiency in the ALG14 enzyme results in incomplete assembly of the lipid linked oligosaccharide (LLO), leading to insufficient N-glycosylation of glycoproteins.

0 trials tagged with this condition →

Congenital myasthenic syndrome 15 0 trials
Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies 0 trials
Myopathy, epilepsy, and progressive cerebral atrophy 0 trials