juvenile cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of cataract that is not apparent at birth but that arises in childhood or adolescence. (Human Phenotype Ontology, HP_0001118)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001118
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2 genes associated with the juvenile cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NF2 neurofibromin 2 (merlin)
RECQL4 RecQ protein-like 4