Conditions / Genetic
Leber congenital amaurosis 3
info · Genetic · ICD-10: H35.5
A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31.
Signs and symptoms
- Visual loss
- Nystagmus
- Constriction of peripheral visual field
- Nyctalopia
Also known as: LCA3