SE-ATLAS

Hereditary retinoblastoma Rare disorder with strabismus Genetic macular dystrophy Early-onset anterior polar cataract Posterior amorphous corneal dystrophy Congenital stromal corneal dystrophy Meesmann corneal dystrophy Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Intermediate uveitis Cogan syndrome X-linked endothelial corneal dystrophy Okihiro syndrome Chondroectodermal dysplasia with night blindness Cancer-associated retinopathy Cryptophthalmia Oculocutaneous albinism type 1 Congenital upper palpebral retraction Anterior uveitis Pediatric-onset glaucoma of genetic origin Conjunctival telangiectasia Aplasia of lacrimal and salivary glands Oculofaciocardiodental syndrome Norrie disease Uveitis Oculocutaneous albinism type 3 Usher syndrome type 1 Benign concentric annular macular dystrophy Fundus pulverulentus Oculoauricular syndrome, Schorderet type IRVAN syndrome Fleck corneal dystrophy Isolated microphthalmia-anophthalmia-coloboma Endophthalmitis Leber hereditary optic neuropathy Bradyopsia Peters anomaly-cataract syndrome SRD5A3-CDG Congenital malformation of the eyelid Inherited retinal disorder Retinitis punctata albescens Idiopathic panuveitis Rare disorder with ptosis Conjunctival hemangioma or hemolymphangioma Ligneous conjunctivitis Non-infectious anterior uveitis Revesz syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Oculocutaneous albinism type 2 Idiopathic macular telangiectasia type 1 Blepharo-cheilo-odontic syndrome Knobloch syndrome Coralliform cataract Stickler syndrome type 1 Posterior polymorphous corneal dystrophy Coats disease Epithelial basement membrane dystrophy X-linked reticulate pigmentary disorder Phacoanaphylactic uveitis Central areolar choroidal dystrophy Spasmus nutans Hypomyelination-congenital cataract syndrome X-linked recessive ocular albinism Isolated distichiasis Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Morning glory disc anomaly Oculocutaneous albinism type 4 Serpiginous choroiditis Septo-optic dysplasia spectrum Eyelid border anomaly Palpebral epidermal tumor Familial retinal arterial macroaneurysm Retinal macular dystrophy type 2 Pigmentation disorder with eye involvement Pigmented conjunctival lesion Syndromic disorder with strabismus Glaucoma associated with neural crest cell migration anomaly Congenital microcoria Unclassified primitive or secondary maculopathy Colobomatous and areolar dystrophy Tolosa-Hunt syndrome Cerulean cataract Central cloudy dystrophy of François Bothnia retinal dystrophy Lisch epithelial corneal dystrophy Colobomatous microphthalmia Oculocutaneous albinism Micro syndrome Sorsby pseudoinflammatory fundus dystrophy Fatty acid hydroxylase-associated neurodegeneration Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Congenital trigeminal anesthesia Familial drusen Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Oculocutaneous albinism type 1B GAPO syndrome Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome Nuclear oculomotor paralysis Congenital eyelid retraction Congenital cornea plana Microblepharon-ablephara syndrome Åland Islands eye disease Distal deletion 6p Palpebral tumor Pellucid marginal degeneration Conjunctival lymphangiectasia Congenital malformation of the eye with glaucoma as a major feature Hypotrichosis with juvenile macular degeneration Autosomal dominant optic atrophy plus syndrome Familial exudative vitreoretinopathy Rare ophthalmic disorder Congenital cataract microcornea with corneal opacity Essential strabismus Bulbar conjunctival dermoid or conjunctival dermolipoma Anterior segment developmental anomaly without extraocular manifestations EEM syndrome Late-onset retinal degeneration Coloboma of macula-brachydactyly type B syndrome Early-onset X-linked optic atrophy Bilateral acute depigmentation of the iris Gyrate atrophy of choroid and retina Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome Congenital ectropion uveae Primary early-onset glaucoma Congenital primary aphakia Rare oculomotor nerve disorder Systemic diseases with panuveitis Microphthalmia, Lenz type Vitreoretinopathy Early-onset partial cataract Precancerous lesion of palpebral epidermis Retinal degeneration-nanophthalmos-glaucoma syndrome Congenital hereditary endothelial dystrophy type I Familial pterygium of the conjunctiva Stickler syndrome type 2 Fuchs endothelial corneal dystrophy Oligocone trichromacy Goldmann-Favre syndrome Gelatinous drop-like corneal dystrophy Corneodermatoosseous syndrome Hereditary benign intraepithelial dyskeratosis Vasoproliferative tumor of the retina Retinoblastoma Isolated congenital megalocornea PEHO syndrome Kandori fleck retina North Carolina macular dystrophy Infectious epithelial keratitis Paraneoplastic uveitis Ocular albinism Isolated congenital sclerocornea Atopic keratoconjunctivitis Myopic macular degeneration Eales disease Toxic maculopathy due to antimalarial drugs Coats plus syndrome WAGR syndrome Idiopathic posterior uveitis Ocular coloboma Benign tumor of palpebral epidermis Blindness-scoliosis-arachnodactyly syndrome Blepharophimosis-ptosis-epicanthus inversus syndrome Disease predisposing to age-related macular degeneration Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome Conjunctival tumor Autosomal recessive Stickler syndrome Early-onset nuclear cataract Goniodysgenesis Dermochondrocorneal dystrophy Corneal dystrophy-perceptive deafness syndrome Palpebral sebaceous gland tumor Retinitis pigmentosa Rare disorder of the lacrimal apparatus Rare isolated myopia Autosomal dominant optic atrophy and peripheral neuropathy Cystoid macular dystrophy Corneoiridogoniodysgenesis Lens position anomaly Aniridia-renal agenesis-psychomotor retardation syndrome MMEP syndrome Sympathetic ophthalmia Aceruloplasminemia Non-infectious posterior uveitis Persistent placoid maculopathy X-linked corneal dermoid Tritanopia Supranuclear eye movement disorder Moebius syndrome Epithelial recurrent erosion dystrophy Muir-Torre syndrome Vitreoretinal degeneration Total early-onset cataract Oguchi disease Juvenile glaucoma Thiel-Behnke corneal dystrophy Keratoconus Bardet-Biedl syndrome Coloboma of eye lens Congenital entropion Congenital hereditary endothelial dystrophy type II Rare refraction anomaly X-linked retinoschisis Corneodysgenesis Aniridia-cerebellar ataxia-intellectual disability syndrome Lens size anomaly Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome Okihiro syndrome due to 20q13 microdeletion Juvenile cataract-microcornea-renal glucosuria syndrome Fuchs heterochromic iridocyclitis Achromatopsia Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome Oculocutaneous albinism type 7 MORM syndrome Birdshot chorioretinopathy Fundus albipunctatus Early-onset non-syndromic cataract Congenital trochlear nerve palsy Stargardt disease Congenital vitreoretinal dysplasia Ectopia lentis-chorioretinal dystrophy-myopia syndrome Cataract-glaucoma syndrome Early-onset posterior polar cataract Optic atrophy-intellectual disability syndrome Congenital glaucoma Rare eyelid malposition disorder Subepithelial mucinous corneal dystrophy Ataxia-oculomotor apraxia type 1 Malignant tumor of palpebral epidermis Coloboma of choroid and retina Acute endophthalmitis Developmental defect of the eye Aniridia Autosomal dominant rhegmatogenous retinal detachment Microphthalmia with brain and digit anomalies Renal coloboma syndrome Congenital ectropion Peters anomaly Palpebral lentiginosis Congenital alacrima Rare hyperopia and astigmatism Autosomal dominant neovascular inflammatory vitreoretinopathy HERNS syndrome Rare disease with glaucoma as a major feature Neurotrophic keratopathy Lens shape anomaly Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Rare genetic eye disease Oculocutaneous or ocular albinism Autosomal dominant optic atrophy Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome Hereditary hyperferritinemia-cataract syndrome Polymicrogyria with optic nerve hypoplasia Chandler syndrome Choroideremia Corneal dystrophy Granular corneal dystrophy type I 3-methylglutaconic aciduria type 3 Familial flecked retinopathy Persistent hyperplastic primary vitreous Coloboma of macula Stickler syndrome Ocular albinism with congenital sensorineural deafness Isolated ectopia lentis Autosomal recessive bestrophinopathy Aniridia-ptosis-intellectual disability-familial obesity syndrome Grayson-Wilbrandt corneal dystrophy Secondary entropion Pigmented palpebral tumor Secretory apparatus of the lacrimal system anomaly Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome Peters plus syndrome Secondary glaucoma due to a proliferation and differentiation anomaly Vogt-Koyanagi-Harada disease Usher syndrome type 2 Occult macular dystrophy Congenital stationary night blindness Pigmented paravenous retinochoroidal atrophy Oculomotor apraxia Hereditary optic neuropathy Hereditary vascular retinopathy Early-onset zonular cataract Axenfeld anomaly Microspherophakia-metaphyseal dysplasia syndrome Reis-Bücklers corneal dystrophy X-linked retinal dysplasia Macular coloboma-cleft palate-hallux valgus syndrome Coloboma of iris Rare inflammatory eye disease Systemic diseases with posterior uveitis Epiblepharon Aniridia-intellectual disability syndrome Ocular albinism with late-onset sensorineural deafness Microphthalmia-anophthalmia-coloboma Canthal anomaly Gardner syndrome Nervous system anomaly with eye involvement Syndromic keratoconus Cerebroretinal vasculopathy Wagner disease Rare disorder with lens opacification Genetic vitreous-retinal disease Oculocutaneous albinism type 6 Duane retraction syndrome Color-vision disease Essential iris atrophy Behr syndrome Lattice corneal dystrophy type I Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Coloboma of optic disc Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Pre-Descemet corneal dystrophy Vernal keratoconjunctivitis Infectious panuveitis Microcornea-corectopia-macular hypoplasia syndrome Aniridia-absent patella syndrome Acute annular outer retinopathy Superior limbic keratoconjunctivitis Idiopathic anterior uveitis Chronic endophthalmitis Cone dystrophy with supernormal rod response Major induction processes eye anomaly High myopia-sensorineural deafness syndrome Palpebral nevus Lacrimal drainage system anomaly Syndromic hyperopia Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Rare lens disease Pigmentation disorder with eye involvement, excluding albinism MRCS syndrome Abnormal eye movements Isolated optic nerve hypoplasia/aplasia Hermansky-Pudlak syndrome due to AP-3 deficiency Autosomal dominant optic atrophy, classic form Anterior segment developmental anomaly Microcornea-glaucoma-absent frontal sinuses syndrome Cogan-Reese syndrome Granular corneal dystrophy type II Progressive cone dystrophy Coloboma of eyelid Alström syndrome Panuveitis Snowflake vitreoretinal degeneration Syndromic oculocutaneous albinism Oculocutaneous albinism type 5 Cataract-microcornea syndrome Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly Syndromic aniridia Butterfly-shaped pigment dystrophy Nanophthalmos Pulverulent cataract Tumor, mesenchymatöser palpebraler Progressive Retinadystrophie durch Retinol-Transportdefekt Schnyder-Hornhautdystrophie Neuromyelitis-optica-Spektrum-Störung Syndromale Mikrophthalmie Typ 5 Zapfen-Stäbchen-Dystrophie Hornhautdystrophie, stromale Amaurosis congenita Leber Primäre Hypomagnesiämie mit Hyperkalziurie, Nephrokalzinoseund schwerer Augenbeteiligung Ankyloblepharon filiforme adnatum, isoliertes Dysplasie, dyssegmentale - Glaukom Ektropion, isoliertes kongenitales Frühgeborenen-Retinopathie Usher-Syndrom Typ 3 Intelligenzminderung-Alakrimie-Achalasie-Syndrom Retinopathie, akute äußere okkulte zonale Mikrophthalmie-Ankyloblepharon-Intelligenzminderung-Syndrom Trochlearislähmung, kongenitale, familiäre Form Musterdystrophien des retinalen Pigmentepithels Uveitis, posteriore, infektiöse Form Epikanthus lateralis/medialis Ataxie, spinozerebelläre, mit okulomotorischer Anomalie Blepharoptose - Myopie - Linsenektopie Neuro-ophthalmologische Krankheit Tumor, palpebraler piliärer Optikusatrophie, isolierte, autosomal-rezessive Adulte foveomakuläre vitelliforme Dystrophie Albinismus, okulokutaner , Typ 1, minimal-pigmentierter Katarakt, syndromale Hornhautdystrophie, superfizielle Schwere Netzhautdystrophie mit Beginn in früher Kindheit Spastische Ataxie - Hornhautdystrophie Uveales Effusions-Syndrom, idiopathisches Kryptophthalmie, isolierte Axenfeld-Rieger-Syndrom Keratitis, idiopathische interstitielle lineare Horner-Syndrom, kongenitales Matthew-Wood-Syndrom Ataxie-Intelligenzminderung-okulomotorische Apraxie-zerebelläre Zysten-Syndrom Augenkrankheit, erworbene, seltene Ophthalmoplegie, chronische externe progressive, maternal-vererbte Endotheliitis Amaurose-Hypertrichose-Syndrom Syndrom der genickten Lidplatte Albinismus, okulokutaner, Typ 1, temperaturempfindlicher Iridokorneales endotheliales Syndrom Systemische Krankheit mit anteriorer Uveitis Keratitis, autosomal-dominante Mikrophthalmie-Hirnatrophie-Syndrom Musterdystrophie, multifokale (vorgetäuschter Fundus flavimaculatus) Idiopathische makuläre Teleangiektasie Typ 3 Retinale arteriovenöse Kommunikation, kongenitale Uveitis, posteriore Sehnerv-Hypoplasie, syndromale Hornhautdystrophie, makuläre Best vitelliforme Makuladegeneration Retinale kapilläre Fehlbildung Mikrophthalmie-lineares Hautdefekt-Syndrom Seltene Krankheiten des palpebralen, lakrimalen und konjunktivalen Systems Optikusatrophie und Katarakt, autosomal-dominante Form Palpebraler Defekt, seltener Okihiro-Syndrom durch Punktmutationen Gonokokkenkonjunktivitis Augenlidanomalie, kinetische Atrophie, bifokale chorioretinale progressive Bindehautanomlie, vaskuläre Hornhautdystrophie, syndromale Aniridie, isolierte Bietti-Kristalldystrophie Optikusatrophie, autosomal-rezessive, Typ 7 Netzhautdystrophie, hereditäre, sonstige Horizontale Blicklähmung mit progredienter Skoliose Blauzapfenmonochromasie Albinismus, okulokutaner, Typ 1A Alakrimie, isolierte kongenitale Chorioretinale Degeneration, helikoid-peripapilläre Zapfendystrophie-Myopie-Syndrom, X-chromosomales Retinoblastom, unilaterales Rieger-Anomalie Herpes simplex-Stromakeratitis Usher-Syndrom Anophthalmie/Mikrophthalmie - Ösophagusatresie Ablepharon-Makrostomie-Syndrom Leber plus-Krankheit Netzhautdystrophie des retinalen Pigmentepithels Syndromales Mikrophthalmie-Anophthalmie-Kolobom Triple-A-Syndrom Katarakt, suturale, früh-beginnende Augenkrankheit bei Differenzierungsanomalie Telekanthus Tumor, palpebraler, mit vaskulärer Fehlbildung EDICT-Syndrom Tumor, neurogener palpebraler Apraxie, okulomotorische, Typ Cogan Bindehautkrankheit, seltene Glaukom, neovaskuläres Hornhautdystrophie, posteriore Gefleckte Retina, benigne familiäre Retinitis pigmentosa, syndromale Pemphigoid, okuläres vernarbendes Vitreoretinochoroidopathie, autosomal-dominante Euryblepharon Uveitis, anteriore, infektiöse Form Agel-Amyloidose