crossed fused renal ectopia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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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.

Symbol Name
KMT2D lysine (K)-specific methyltransferase 2D
SALL4 spalt-like transcription factor 4