Cerulean cataract Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Cerulean cataracts are a kind of congenital cataract having peripheral bluish and white opacifications in concentric layers with occasional central lesions arranged radially. Although the opacities may be observed during fetal development and childhood, usually visual acuity is only mildly reduced until adulthood, when lens extraction is generally necessary. (Human Phenotype Ontology, HP_0007976)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537955
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Genes

2 genes/proteins associated with the disease Cerulean cataract from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CRYBB2 crystallin, beta B2 2.88009
CCA1 cataract, congenital, cerulean type, 1 2.88009