In a total of 35 subjects with KIF11 variants, chorioretinal dysplasia was found in 44.2% (31/70) of eyes and was the leading phenotype of KIF11-associated retinopathy, followed by retinal folds (34.3%, 24/70) and retinal degeneration (12.9%, 9/70). Here, KIF11 is linked to retinal degeneration.