|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A developmental anomaly in which the kidneys are fused and localized on the same side of the midline. This anomaly is thought to result from disruption of the normal embryologic migration of the kidneys. (Human Phenotype Ontology, HP_0004736)|
|Downloads & Tools|
2 genes associated with the crossed fused renal ectopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.