SE-ATLAS

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