The retinal phenotype of BBS1 is typically described as RP-like rod-cone dystrophy (Grudzinska Pechhacker et al., 2021); however, BBS10 may occur as a cone-rod dystrophy, or even an isolated cone dystrophy (Grudzinska Pechhacker et al., 2021). The gene discussed is BBS10; the disease is retinitis pigmentosa 1.