|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome (see this term) characterized clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy. (Orphanet Rare Disease Ontology, Orphanet_263494)|
|Downloads & Tools|
1 genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.
|DPM3||dolichyl-phosphate mannosyltransferase polypeptide 3||2.88009|