Cataract 40

Alternative Names

  • CTRCT40
  • Cataract 40 With Or Without Microcornea
  • Cataract, Congenital, X-Linked
  • CXN
  • Cataract, Congenital Total, With Posterior Sutural Opacities In Heterozygotes
  • CCT

Associated Genes

NHS Gene
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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Congenital malformations of eye, ear, face and neck

OMIM Number

302200

Mode of Inheritance

X-linked

Gene Map Locus

Xp22.2-p22.13

Description

Cataract 40 is an X-linked congenital ocular disorder. Symptoms in affected males include lamellar, zonular or perinuclear cataracts, severe visual impairment and pronounced microcornea while characteristics in heterozygous females include posterior suture and/or posterior stellate cataracts, and normal or slightly impaired vision. 

Epidemiology in the Arab World

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