Conditions / Genetic
cataract 21 multiple types
info · Genetic · ICD-10: Q12.0
A cataract that has_material_basis_in heterozygous mutation in the MAF gene on chromosome 16q23.
Signs and symptoms
- Cortical pulverulent cataract
- Cerulean cataract
- Microcornea
- Retinal detachment
- Macular hypoplasia
- Corneal opacity
- Iris coloboma
- Peters anomaly
- High myopia
Also known as: CTRCT21; cataract 21 multiple types with or without microcornea