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GTR Home > Conditions/Phenotypes > Cataract 16 multiple types

Summary

Mutations in the CRYAB gene have been found to cause multiple types of cataract, which have been described as congenital posterior polar, congenital lamellar, and juvenile. Autosomal dominant and autosomal recessive forms have been described. The preferred title/symbol of this entry was formerly 'Cataract, Posterior Polar, 2; CTPP2.' [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: CMD1II, CRYA2, CTPP2, CTRCT16, HEL-S-101, HSPB5, MFM2, CRYAB
    Summary: crystallin alpha B

Clinical features

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