reduced renal corticomedullary differentiation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced differentiation between renal cortex and medulla on diagnostic imaging. (Human Phenotype Ontology, HP_0005565)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005565
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Genes

2 genes associated with the reduced renal corticomedullary differentiation 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
NIPBL Nipped-B homolog (Drosophila)