papillorenal syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Renal coloboma syndrome (RCS) is a genetic condition characterized by optic nerve dysplasia and renal hypodysplasia. (Orphanet Rare Disease Ontology, Orphanet_1475)
External Link http://www.omim.org/entry/120330
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Genes

1 genes associated with the papillorenal syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PAX2 paired box 2