Disease & disorder

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.

Outbreak surveillance

Global reported events

Explore recent public health notices potentially related to ALG14-congenital disorder of glycosylation. Results are keyword matches, not yet verified disease-to-outbreak relationships.

View ALG14-congenital disorder of glycosylation on the outbreak map →
Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms1
Advertisement

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.