CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/300896
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Genes

1 genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2