impairment of galactose metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An impairment of galactose metabolism. (Human Phenotype Ontology, HP_0004915)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004915
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Genes

5 genes associated with the impairment of galactose metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GALE UDP-galactose-4-epimerase
GALK1 galactokinase 1
GALT galactose-1-phosphate uridylyltransferase
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
TTC37 tetratricopeptide repeat domain 37