nephroblastomatosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Presence of persistent islands of renal blastema in the postnatal kidney. Nephroblastomatosis represents a complex abnormality of nephrogenesis and has been defined as the persistence of metanephricblastema into infancy and childhood. (Human Phenotype Ontology, HP_0008643)
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2 genes associated with the nephroblastomatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator
DIS3L2 DIS3 like 3'-5' exoribonuclease 2