fetal polyuria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally increased production of urine by the fetus resulting in polyhydramnios. (Human Phenotype Ontology, HP_0001563)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001563
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Genes

5 genes associated with the fetal polyuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BSND barttin CLCNK-type chloride channel accessory beta subunit
CLCNKA chloride channel, voltage-sensitive Ka
CLCNKB chloride channel, voltage-sensitive Kb
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1