|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Congenital disorder of glycosylation type IIi (CDG-IIi) is an extremely rare form of CDG syndrome (see this term) characterized clinically in the single reported case to date by moderate mental retardation with slow and inarticulate speech, truncal ataxia, and mild hypotonia. (Orphanet Rare Disease Ontology, Orphanet_263487)|
|Downloads & Tools|
1 genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.
|COG5||component of oligomeric golgi complex 5||2.88009|