SE-ATLAS

Adult neuronal ceroid lipofuscinosis Adult-onset foveomacular vitelliform dystrophy Alström syndrome Aniridia Autosomal recessive bestrophinopathy Autosomal recessive chorioretinopathy-microcephaly syndrome Axenfeld-Rieger syndrome Bardet-Biedl syndrome Benign concentric annular macular dystrophy Best vitelliform macular dystrophy Blau syndrome Butterfly-shaped pigment dystrophy CHARGE syndrome CLN1 disease CLN10 disease CLN11 disease CLN13 disease CLN4A disease CLN4B disease CLN6 disease Cat-eye syndrome Cataract-microcornea syndrome Central areolar choroidal dystrophy Choroideremia Cohen syndrome Coloboma of macula Colobomatous and areolar dystrophy Cone dystrophy with supernormal rod response Cone rod dystrophy Congenital cataract microcornea with corneal opacity Congenital ectropion Congenital entropion Congenital glaucoma Congenital hereditary endothelial dystrophy type II Congenital neuronal ceroid lipofuscinosis Congenital ptosis Congenital stationary night blindness Corneal dystrophy Cornelia de Lange syndrome Cystoid macular dystrophy Duane retraction syndrome Familial benign flecked retina Familial exudative vitreoretinopathy Fuchs endothelial corneal dystrophy Fuchs heterochromic iridocyclitis Galactosialidosis Genetic macular dystrophy Goldenhar syndrome Goldmann-Favre syndrome Graft versus host disease Gyrate atrophy of choroid and retina Horizontal gaze palsy with progressive scoliosis Hypotrichosis with juvenile macular degeneration Idiopathic infantile nystagmus Infantile Refsum disease Infantile neuronal ceroid lipofuscinosis Inherited retinal disorder Isolated aniridia Joubert syndrome Joubert syndrome with oculorenal defect Juvenile glaucoma Juvenile neuronal ceroid lipofuscinosis Kearns-Sayre syndrome Late infantile neuronal ceroid lipofuscinosis Late-onset retinal degeneration Leber hereditary optic neuropathy Ligneous conjunctivitis Limbal stem cell deficiency Microcephaly-lymphedema-chorioretinopathy syndrome Mucolipidosis type IV Multifocal pattern dystrophy simulating fundus flavimaculatus Neuronal ceroid lipofuscinosis Niemann-Pick disease type C North Carolina macular dystrophy Occult macular dystrophy Oguchi disease Pattern dystrophy Peters anomaly Pigmented paravenous retinochoroidal atrophy Progressive cone dystrophy Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa Rare disorder of the lacrimal apparatus Reticular dystrophy of the retinal pigment epithelium Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Retinitis pigmentosa Severe early-childhood-onset retinal dystrophy Sorsby pseudoinflammatory fundus dystrophy Stargardt disease Stickler syndrome Syndromic aniridia Syndromic rod-cone dystrophy Toxocariasis Tubulointerstitial nephritis and uveitis syndrome Unclassified familial retinal dystrophy Unclassified primitive or secondary maculopathy Usher syndrome Usher syndrome type 1 Usher syndrome type 2 Usher syndrome type 3 Uveitis X-linked retinoschisis