SE-ATLAS

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