cerulean cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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://compbio.charite.de/hpoweb/showterm?id=HP:0007976
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2 genes associated with the cerulean cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CRYBB2 crystallin, beta B2
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog