?congenital disorder of glycosylation, type ix Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615597
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Genes

1 genes associated with the ?congenital disorder of glycosylation, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
STT3B STT3B, subunit of the oligosaccharyltransferase complex (catalytic)