lamellar cataracts Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a concentric lens opacity which is limited to layers of the cortex, affecting one lamella or zonule of an otherwise clear lens; usually congenital (Mammalian Phenotype Ontology, MP_0010262)
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1 gene mutations causing the lamellar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CRYGB crystallin, gamma B