dense posterior cortical cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of posterior cortical cataract characterized by dense lenticular opacities. (Human Phenotype Ontology, HP_0007948)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007948
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Genes

1 genes associated with the dense posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
OCRL oculocerebrorenal syndrome of Lowe