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