abnormal urine magnesium concentration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal concentration of magnesium the urine. (Human Phenotype Ontology, HP_0012607)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012607
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5 genes associated with the abnormal urine magnesium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLDN16 claudin 16
CLDN19 claudin 19
FXYD2 FXYD domain containing ion transport regulator 2
IFT122 intraflagellar transport 122
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3