Conditions / Genetic
posterior polymorphous corneal dystrophy 3
info · Genetic · ICD-10: H18.50
A posterior polymorphous corneal dystrophy that has_material_basis_in heterozygous mutation in the ZEB1 gene on chromosome 10p11.22.
Signs and symptoms
- Keratoconus
- Ectopia pupillae
- Corneal dystrophy
- Reduced visual acuity
- Inguinal hernia
- Corneal guttata
Also known as: PPCD3