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cataract 22 multiple types

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Disease Overview

Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYBB3 gene.

Synonyms

  • CATCN2
  • CRYBB3 early-onset non-syndromic cataract
  • CTRCT22
  • autosomal recessive congenital nuclear cataract 2
  • cataract 22
  • cataract 22, multiple types
  • cataract, congenital nuclear, autosomal recessive 2
  • early-onset non-syndromic cataract caused by mutation in CRYBB3
OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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