congenital nuclear cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of congenital cataract in which the opacities are confined to a small central area within the embryonic or fetal nuclei of the Iens. The remaining lens is clear. (Human Phenotype Ontology, HP_0008024)
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3 genes associated with the congenital nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CRYGC crystallin, gamma C
FTL ferritin, light polypeptide
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)