absence of renal corticomedullary differentiation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A lack of differentiation between renal cortex and medulla on diagnostic imaging. (Human Phenotype Ontology, HP_0005564)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005564
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Genes

2 genes associated with the absence of renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
INVS inversin
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)