GTR Home > Conditions/Phenotypes > Posterior polymorphous corneal dystrophy 3

Summary

Any posterior polymorphous corneal dystrophy in which the cause of the disease is a mutation in the ZEB1 gene. [from MONDO]

Available tests

15 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: AREB6, BZP, DELTAEF1, FECD6, NIL2A, PPCD3, TCF8, ZFHEP, ZFHX1A, ZEB1
    Summary: zinc finger E-box binding homeobox 1

Clinical features

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