posterior cortical cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A cataract that affects the posterior part of the cortex of the lens. (Human Phenotype Ontology, HP_0010924)
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1 genes associated with the 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