enuresis Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Lack of the ability to control the urinary bladder leading to involuntary urination at an age where control of the bladder should already be possible. (Human Phenotype Ontology, HP_0000805)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000805
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Genes

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

Symbol	Name
DLG3	discs, large homolog 3 (Drosophila)
FAM20A	family with sequence similarity 20, member A
HPSE2	heparanase 2 (inactive)
KCNJ10	potassium channel, inwardly rectifying subfamily J, member 10
LRIG2	leucine-rich repeats and immunoglobulin-like domains 2
NPHP3	nephronophthisis 3 (adolescent)
SLC5A2	solute carrier family 5 (sodium/glucose cotransporter), member 2