Conditions / Genetic
cataract 9 multiple types
info · Genetic · ICD-10: Q12.0
A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.
Signs and symptoms
- Strabismus
- Cataract
- Nystagmus
- Developmental cataract
- Amblyopia
- Visual impairment
- Glaucoma
- Microcornea
- Iris coloboma
- Microphthalmia
Also known as: CTRCT9; cataract 9 multiple types with or without microcornea