SE-ATLAS

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