SE-ATLAS

Progressive cone dystrophy Cone rod dystrophy Leber hereditary optic neuropathy Retinitis pigmentosa Bardet-Biedl syndrome Autosomal dominant optic atrophy and peripheral neuropathy Adult-onset foveomacular vitelliform dystrophy Inherited retinal disorder Sorsby pseudoinflammatory fundus dystrophy Autosomal dominant optic atrophy plus syndrome Stargardt disease Stickler syndrome Occult macular dystrophy Best vitelliform macular dystrophy Bietti crystalline dystrophy Peters anomaly North Carolina macular dystrophy Choroideremia Coats disease Autosomal recessive isolated optic atrophy Alström syndrome Leber congenital amaurosis Usher syndrome Hypotrichosis with juvenile macular degeneration Goldmann-Favre syndrome Congenital stationary night blindness Iridocorneal endothelial syndrome Familial drusen Central areolar choroidal dystrophy Axenfeld anomaly Abetalipoproteinemia Optic pathway glioma Isolated aniridia Oculocutaneous albinism type 4 Pituitary adenoma Senior-Loken syndrome Ocular albinism Isolated macular dystrophy Sturge-Weber syndrome Norrie disease Granular corneal dystrophy type I Congenital glaucoma Corneal dystrophy Achromatopsia Refsum disease Familial exudative vitreoretinopathy Wagner disease Wolfram syndrome Recurrent idiopathic neuroretinitis Isolated optic neuritis Juvenile neuronal ceroid lipofuscinosis Meningioma Retinopathy of prematurity Incontinentia pigmenti Kearns-Sayre syndrome X-linked retinoschisis Fuchs endothelial corneal dystrophy Birdshot chorioretinopathy Helicoid peripapillary chorioretinal degeneration Oculocutaneous albinism type 1 Autosomal dominant optic atrophy, classic form