Mutations in AIPL1 are associated with Leber congenital amaurosis, a severe form of inherited retinal degeneration (Yadav et al., 2017; Rashid et al., 2020; Sacristan-Reviriego et al., 2020; Xu et al., 2020). The gene discussed is AIPL1; the disease is Leber congenital amaurosis.