To access the data, click or select the words “Appendix 2.” ACHM, achromatopsia; ARB, autosomal recessive Bestrophinopathy; BAF- blue autofluoresence; BSP, bone spicule pigmentation; CF, counting fingers; CRD, cone-rod dystrophy; ERM, epiretinal membrane; F, female; FAF, fundus autofluorescence; HL, hearing loss; HM, hand motion; LCA, Leber congenital amaurosis; M, male; MD, macular dystrophy; MFERG: multifocal electroretinography; NA, not available; NLP, no light perception; OCT, optical coherence tomography; OD, right eye; OS, left eye; ON, optic nerve, OU, both eyes; PD, pattern dystrophy; RD, retinal dystrophy; RP, retinitis pigmentosa; RPE, retinal pigment epithelium, SS, short stature; STGD, Stargardt disease; VEP, visual evoked potentials; y, years ^aFFERG: full-field electroretinogram; NR, non-recordable, WNR: within normal range, MiR: mildly reduced, MR: moderately reduced (1%–5% of normal range); SR, severely reduced (<1% of normal range); ND, non-detectable ^b Stargardt typing according to fundus autofluoresence distribution of pathologic findings ^{8 c} Type unknown since FAF is unavailable