|Dataset||OMIM 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 associated with the congenital disorder of glycosylation, type io phenotype from the curated OMIM Gene-Disease Associations dataset.
|DPM3||dolichyl-phosphate mannosyltransferase polypeptide 3|