SE-ATLAS

Inherited retinal disorder Sorsby pseudoinflammatory fundus dystrophy EEM syndrome Aceruloplasminemia Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Gyrate atrophy of choroid and retina Stargardt disease Familial flecked retinopathy Occult macular dystrophy Progressive retinal dystrophy due to retinol transport defect Best vitelliform macular dystrophy Bothnia retinal dystrophy Cone dystrophy with supernormal rod response MORM syndrome Severe early-childhood-onset retinal dystrophy Pattern dystrophy Ehlers-Danlos syndrome Unclassified familial retinal dystrophy Syndromic rod-cone dystrophy Genetic macular dystrophy Benign concentric annular macular dystrophy Unclassified primitive or secondary maculopathy Colobomatous and areolar dystrophy Acquired pseudoxanthoma elasticum Autosomal recessive bestrophinopathy Pigmented paravenous retinochoroidal atrophy Leber congenital amaurosis Amaurosis-hypertrichosis syndrome Helicoid peripapillary chorioretinal degeneration Usher syndrome Åland Islands eye disease Foveal hypoplasia-presenile cataract syndrome Retinal macular dystrophy type 2 Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Hypotrichosis with juvenile macular degeneration Late-onset retinal degeneration Retinal degeneration-nanophthalmos-glaucoma syndrome Goldmann-Favre syndrome Pseudoxanthoma elasticum X-linked retinal dysplasia Progressive bifocal chorioretinal atrophy Revesz syndrome Refsum disease Oligocone trichromacy Oguchi disease Cystoid macular dystrophy Progressive cone dystrophy Hermansky-Pudlak syndrome due to AP-3 deficiency Cone rod dystrophy Familial benign flecked retina Retinitis pigmentosa X-linked retinoschisis Bardet-Biedl syndrome Ectopia lentis-chorioretinal dystrophy-myopia syndrome MRCS syndrome Adult-onset foveomacular vitelliform dystrophy