renal corticomedullary cysts Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of multiple cysts at the border between the renal cortex and medulla. (Human Phenotype Ontology, HP_0000108)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000108
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Genes

6 genes associated with the renal corticomedullary cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MUC1 mucin 1, cell surface associated
NPHP1 nephronophthisis 1 (juvenile)
NPHP3 nephronophthisis 3 (adolescent)
NPHP4 nephronophthisis 4
TMEM67 transmembrane protein 67
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial