congenital nuclear cataract Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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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Genes

1 genes associated with the disease congenital nuclear cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CRYBA1 crystallin, beta A1