|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A lack of differentiation between renal cortex and medulla on diagnostic imaging. (Human Phenotype Ontology, HP_0005564)|
|Downloads & Tools|
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.