cataract 17 multiple types

A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B1 crystallin gene (CRYBB1) on chromosome 22q12.

Signs and symptoms

• Pulverulent cataract
• Nuclear cataract
• Nystagmus
• Developmental cataract
• Reduced visual acuity
• Microcornea
• Amblyopia

Also known as: CTRCT17