ALG14-congenital disorder of glycosylation

MONDO:0100559

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

Also known as: ALG14-CDG

0 clinical trials for this condition and its sub-types, 0 tagged with ALG14-congenital disorder of glycosylation itself.

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↑ Congenital disorder of glycosylation (36)

Sub-types of ALG14-congenital disorder of glycosylation

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

Including sub-types (0) Tagged with ALG14-congenital disorder of glycosylation (0)

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