hyposthenuria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally low urinary specific gravity, i.e., reduced concentration of solutes in the urine. (Human Phenotype Ontology, HP_0003158)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003158
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Genes

3 genes associated with the hyposthenuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
NPHP1 nephronophthisis 1 (juvenile)
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1