congenital disorder of glycosylation, type iig Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital disorder of glycosylation type IIg (CDG-IIg) is an extremely rare form of CDG syndrome (see this term) characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation, and variable facial dysmorphism. (Orphanet Rare Disease Ontology, Orphanet_263508)
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1 genes associated with the congenital disorder of glycosylation, type iig phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
COG1 component of oligomeric golgi complex 1