SE-ATLAS

Fuchs endothelial corneal dystrophy Cone dystrophy with supernormal rod response Leber congenital amaurosis Panuveitis Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Bothnia retinal dystrophy Progressive retinal dystrophy due to retinol transport defect Helicoid peripapillary chorioretinal degeneration X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome Microcornea-myopic chorioretinal atrophy-telecanthus syndrome MORM syndrome Syndromic rod-cone dystrophy Unclassified familial retinal dystrophy Progressive bifocal chorioretinal atrophy Isolated inherited retinal disorder Oguchi disease Brachydactyly-short stature-retinitis pigmentosa syndrome Uveitis Pigmented paravenous retinochoroidal atrophy Åland Islands eye disease Aceruloplasminemia Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Autosomal recessive bestrophinopathy Familial benign flecked retina Revesz syndrome Severe early-childhood-onset retinal dystrophy Retinitis pigmentosa Martinique crinkled retinal pigment epitheliopathy Retinal degeneration-nanophthalmos-glaucoma syndrome Anterior uveitis Posterior uveitis X-linked retinal dysplasia Ectopia lentis-chorioretinal dystrophy-myopia syndrome Genetic macular dystrophy Intermediate uveitis Oligocone trichromacy Syndromic inherited retinal disorder Atrophie gyrée choriorétinienne Maladie rétinienne héréditaire Syndrome MRCS Syndrome de choriorétinopathie-microcéphalie autosomique récessive Syndrome de microcéphalie-lymphoedème-choriorétinopathie Dégénérescence rétinienne d'apparition tardive Syndrome d'amaurose-hypertrichose Dégénérescence cérébello-rétinienne infantile