SE-ATLAS

3-methylglutaconic aciduria type 3 AGel amyloidosis Ablepharon macrostomia syndrome Abnormal eye movements Aceruloplasminämie Achromatopsie Acute annular outer retinopathy Acute endophthalmitis Aderhautdystrophie, areoläre zentrale Adult-onset foveomacular vitelliform dystrophy Albinismus, okulokutaner Albinismus, okulokutaner , Typ 1, minimal-pigmentierter Albinismus, okulokutaner, Typ 4 Albinismus, okulokutaner, Typ 5 Alström syndrome Amaurosis-hypertrichosis syndrome Aniridia-absent patella syndrome Aniridia-intellectual disability syndrome Aniridia-ptosis-intellectual disability-familial obesity syndrome Aniridie Aniridie-Nierenagenesie-psychomotorische Retardierung-Syndrom Aniridie-zerebelläre Ataxie-Intelligenzminderung-Syndrom Anomalie des vorderen Augensegmentes ohne extraokuläre Manifestationen Anophthalmia/microphthalmia-esophageal atresia syndrome Anterior segment developmental anomaly Aphakie, kongenitale primäre Aplasia of lacrimal and salivary glands Ataxie mit okulomotorischer Apraxie Typ 1 Ataxie-Intelligenzminderung-okulomotorische Apraxie-zerebelläre Zysten-Syndrom Atopic keratoconjunctivitis Atrophia gyrata der Chorioidea und Retina Augenanomalie bei Anlagestörung Augenlider, Fehlstellung der Augenlidkante, Anomalie der Autosomal dominant keratitis Autosomal dominant neovascular inflammatory vitreoretinopathy Autosomal dominant optic atrophy Autosomal dominant optic atrophy and cataract Autosomal dominant optic atrophy, classic form Autosomal dominant rhegmatogenous retinal detachment Autosomal dominant vitreoretinochoroidopathy Autosomal recessive bestrophinopathy Autosomal recessive isolated optic atrophy Autosomal recessive optic atrophy, OPA7 type Axenfeld-Anomalie Axenfeld-Rieger syndrome Bakrania-Ragge-Syndrom Bardet-Biedl-Syndrom Basalmembrandystrophie, epitheliale Behr syndrome Benign concentric annular macular dystrophy Beninger Tumor der palpebralen Epidermis Best vitelliform macular dystrophy Bietti crystalline dystrophy Bindehautläsion, pigmentierte Bindehauttumor Blepharo-cheilo-odontic syndrome Blepharophimose-Ptosis-Epicanthus inversus-Syndrom Blepharoptosis-myopia-ectopia lentis syndrome Blindness-scoliosis-arachnodactyly syndrome Blue cone monochromatism Bothnia retinal dystrophy Bradyopsia Butterfly-shaped pigment dystrophy Cancer-associated retinopathy Canthal anomaly Cataract-microcornea syndrome Central cloudy dystrophy of François Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Cerebroretinal vasculopathy Cerulean cataract Chandler syndrome Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Chondroektodermale Dysplasie mit Nachtblindheit Chorioideremie Chorioretinopathie Typ Birdshot Chronic endophthalmitis Coats disease Coats plus syndrome Cogan syndrome Cogan-Reese syndrome Coloboma of eyelid Coloboma of macula Coloboma of optic disc Colobomatous and areolar dystrophy Colobomatous microphthalmia Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome Color-vision disease Cone dystrophy with supernormal rod response Cone rod dystrophy Congenital Horner syndrome Congenital alacrima Congenital ectropion Congenital eyelid retraction Congenital malformation of the eye with glaucoma as a major feature Congenital malformation of the eyelid Congenital retinal arteriovenous communication Congenital stationary night blindness Congenital stromal corneal dystrophy Congenital trigeminal anesthesia Congenital upper palpebral retraction Conjunctival hemangioma or hemolymphangioma Conjunctival lymphangiectasia Conjunctival telangiectasia Conjunctival vascular anomaly Cornea plana, kongenitale Corneal endotheliitis Corneogoniodysgenesie Corneoiridogoniodysgenesie Cryptophthalmia Dermoid/Dermolipom, konjunktivales Developmental defect of the eye Distal deletion 6p Distichiasis, isolierte Duane retraction syndrome Dysplasie, vitreoretinale, kongenitale Dyssegmental dysplasia-glaucoma syndrome Dystrophie, dermo-chondro-corneale EDICT syndrome EEM-Syndrom Eales-Krankheit Early-onset anterior polar cataract Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Early-onset sutural cataract Ectopia lentis, isolierte Ectopia lentis-chorioretinale Dystrophie-Myopie-Syndrom Ektropion uveae, kongenitales Endophthalmitis Endothel-Hornhautdystrophie, X-chromosomale Endotheldystrophie, hereditäre kongenitale 1 Endotheldystrophie, hereditäre kongenitale, Typ II Endotheliale Hornhautdystrophie Fuchs Entropium, kongenitales Entropium, sekundäres Epiblepharon Epicanthal fold Essential iris atrophy Essential strabismus Euryblepharon Familial benign flecked retina Familial congenital palsy of trochlear nerve Familial drusen Familial flecked retinopathy Fettsäure-Hydroxylase-assoziierte Neurodegeneration Fleck corneal dystrophy Fuchs Heterochromie-Iridozyklitis Fundus albipunctatus Fundus pulverulentus GAPO-Syndrom Gardner syndrome Gefleckte Retina nach Kandori Genetic macular dystrophy Genetic vitreous-retinal disease Glaukom, juveniles Glaukom, kongenitales Glaukom, primäres Glaukom, sekundäres durch Proliferierungs- und Differenzierungsanomalien Glaukom-Ektopia lentis-Mikrosphärophakie-steife Gelenke-Kleinwuchs-Syndrom Goldmann-Favre-Syndrom Goniodysgenesie Gonococcal conjunctivitis Granular corneal dystrophy type I Granular corneal dystrophy type II Grayson-Wilbrandt corneal dystrophy HERNS-Syndrom Helicoid peripapillary chorioretinal degeneration Hereditary benign intraepithelial dyskeratosis Hereditary retinoblastoma Hereditäre Hyperferritinämie-Katarakt-Syndrom Hermansky-Pudlak-Syndrom durch AP-3-Defizienz Herpes simplex virus stromal keratitis High myopia-sensorineural deafness syndrome Horizontal gaze palsy with progressive scoliosis Hornhautdystrophie Hornhautdystrophie - Schallempfindungs-Schwerhörigkeit Hornhautdystrophie, gelatinöse tropfenförmige Hornhautdystrophie, muzinöse subepitheliale Hornhautdystrophie, polymorphe posteriore Hypomyelinisierung - kongenitale Katarakt Hypotrichose - juvenile Makuladegeneration IRVAN syndrome Idiopathic anterior uveitis Idiopathic macular telangiectasia type 3 Idiopathic panuveitis Idiopathic posterior uveitis Idiopathic uveal effusion syndrome Idiopathische makuläre Teleangiektasie Typ 1 Infectious anterior uveitis Infectious epithelial keratitis Infectious panuveitis Inherited retinal disorder Intelligenzminderung-Alakrimie-Achalasie-Syndrom Intraepitheliale korneale Dyskeratose-palmoplantare Hyperkeratose-laryngeale Dyskeratose-Syndrom Iridocorneal endothelial syndrome Irisdepigmentierung, akute bilaterale Iriskolobom Isolated aniridia Isolated ankyloblepharon filiforme adnatum Isolated congenital alacrima Isolated congenital ectropion Isolated cryptophthalmia Isolated microphthalmia-anophthalmia-coloboma Juvenile Katarakt-Mikrokornea-renale Glukosurie-Syndrom Katarakt, kongenitale - Mikrokornea - Hornhauttrübung Katarakt, koralliforme Katarakt, nicht-syndromale, kongenitale Katarakt, nukleäre, früh-beginnende Katarakt, partielle, früh-beginnende Katarakt, posteriore polare, früh-beginnende Katarakt, totale, früh-beginnende Katarakt, zonuläre, früh-beginnende Katarakt-Glaukom-Syndrom Keratitis, idiopathische interstitielle lineare Keratokonus Keratopathie, neurotrophe Kinetic eyelid anomaly Knobloch syndrome Kolobom der Chorioidea und Retina Kolobom des Auges Korneales Dermoid, X-chromosomales Korneo-dermato-ossäres-Syndrom Krankheit mit Prädisposition für altersabhängige Makuladegeneration Lacrimal drainage system anomaly Lattice corneal dystrophy type I Leber congenital amaurosis Leber hereditary optic neuropathy Leber plus disease Lens shape anomaly Ligneous conjunctivitis Linsenanomalie (Größe) Linsenanomalie (Position) Linsenkolobom Lisch epithelial corneal dystrophy MMEP-Syndrom MORM-Syndrom MRCS syndrome Macular corneal dystrophy Makroaneurysmen, arterielle retinale, familiäre Form Makula-Kolobom - Brachydaktylie Typ B Makuladystrophie, okkulte Makuladystrophie, zystoide Makulakolobom-Gaumenspalte-Hallux valgus-Syndrom Makulopathie, persistierende plakoide Makulopathie, primäre oder sekundäre, sonstige Matthew-Wood syndrome Meesmann corneal dystrophy Megalokornea - Sphärophakie - sekundäres Glaukom Megalokornea, isolierte kongenitale Mesenchymatous palpebral tumor Microblepharon-ablephara syndrome Microcornea-corectopia-macular hypoplasia syndrome Microcornea-glaucoma-absent frontal sinuses syndrome Microphthalmia with linear skin defects syndrome Microphthalmia-ankyloblepharon-intellectual disability syndrome Microphthalmia-anophthalmia-coloboma Microphthalmia-brain atrophy syndrome Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome Microspherophakia-metaphyseal dysplasia syndrome Migrationsanomalie der Neuralleistenzellen mit Glaukom Mikro-Syndrom Mikrokorie, kongenitale Mikrokornea-Vorderer Lentikonus-persistierender primärer Vitreus-Kolobom-Syndrom Mikrokornea-myopische chorioretinale Atrophie-Telekanthus-Syndrom Mikrophthalmie Typ Lenz Mikrotie-Augenkolobom-imperforierter nasolakrimaler Gang-Syndrom Mitochondrial DNA-related progressive external ophthalmoplegia Moebius-Syndrom Morning glory disc anomaly Muir-Torre-Syndrom Multifocal pattern dystrophy simulating fundus flavimaculatus Myopic macular degeneration Myopie, isolierte, seltene Nanophthalmos Neovascular glaucoma Nervous system anomaly with eye involvement Netzhautdegeneration-Nanophthalmus-Glaukom-Syndrom Netzhautdystrophie, spät beginnende Neuro-ophthalmological disease Neurogenic palpebral tumor Neuromyelitis optica spectrum disorder Non-hereditary retinoblastoma Non-infectious anterior uveitis Norrie disease North-Carolina-Makuladystrophie Nuclear oculomotor paralysis Ocular albinism Ocular albinism with congenital sensorineural deafness Ocular albinism with late-onset sensorineural deafness Ocular cicatricial pemphigoid Ocular motor apraxia, Cogan type Oculocutaneous albinism type 1 Oculocutaneous albinism type 1A Oculocutaneous albinism type 1B Oculocutaneous albinism type 2 Oculocutaneous albinism type 3 Oculocutaneous albinism type 6 Oculocutaneous albinism type 7 Oculocutaneous or ocular albinism Oculofaciocardiodental syndrome Oguchi-Krankheit Okihiro syndrome Okihiro syndrome due to a point mutation Okihiro-Syndrom durch Monosomie 20q13 Okuloaurikuläres Syndrom Typ Schorderet Okulokutaner Albinismus, syndromaler Okulomotorische Apraxie und verwandte okulomotorische Störungen Okulomotorische Lähmung Oligocone-Trichromasie Optic atrophy-intellectual disability syndrome Optikus-Neuropathie, hereditäre Optikusatrophie plus-Syndrom, autosomal-dominantes Optikusatrophie und periphere Neuropathie, autosomal-dominant Optikusatrophie, X-chromosomale, mit frühem Beginn PEHO-Syndrom Palpebral lentiginosis Palpebral nevus Palpebral piliary tumor Palpebral tumor Palpebral tumor with a vascular malformation Palpebrale Epidermis, maligner Tumor der Palpebrale Epidermis, präkanzeröse Läsion der Panuveitis Paralyse, okulomotorische supranukleäre Paraneoplastic uveitis Pattern dystrophy Pediatric-onset glaucoma of genetic origin Pellucid marginal degeneration Persistent hyperplastic primary vitreous Peters anomaly-cataract syndrome Peters plus syndrome Peters-Anomalie Phacoanaphylactic uveitis Pigmentation disorder with eye involvement, excluding albinism Pigmentierte paravenöse retinochoroidale Atrophie Pigmentierungsstörung mit assoziierter Augenbeteiligung Polymicrogyria with optic nerve hypoplasia Posterior amorphous corneal dystrophy Posterior corneal dystrophy Pre-Descemet corneal dystrophy Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Progressive Retinadystrophie durch Retinol-Transportdefekt Progressive bifocal chorioretinal atrophy Progressive cone dystrophy Pterygium conjunctivae, familiäre Form Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Pulverulent cataract Rare acquired eye disease Rare disease with glaucoma as a major feature Rare disorder with conjunctival involvement as a major feature Rare disorder with lens opacification Rare disorder with ptosis Rare disorder with strabismus Rare eye disease due to a differentiation anomaly Rare genetic eye disease Rare hyperopia and astigmatism Rare inflammatory eye disease Rare lens disease Rare ophthalmic disorder Rare palpebral disorder Rare palpebral, lacrimal system and conjunctival disease Refraktionsstörun, seltene Reis-Bücklers-Hornhautdystrophie Renales-Kolobom-Syndrom Reticular dystrophy of the retinal pigment epithelium Retinal capillary malformation Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome Retinal macular dystrophy type 2 Retinale Vaskulopathie mit zerebraler Leukoenzephalopathie und systemischen Manifestationen Retinitis pigmentosa Retinitis punctata albescens Retinoblastom Retinopathie, akute äußere okkulte zonale Retinopathie, exsudative familiäre Retinopathie, hereditäre vaskuläre Retinopathy of prematurity Retinoschisis, X-chromosomale Revesz syndrome Rezidivierende Epithelerosions-Dystrophie Rieger anomaly SRD5A3-CDG Schnyder corneal dystrophy Schwere Netzhautdystrophie mit Beginn in früher Kindheit Sehnerv-Hypoplasie/Aplasie, isolierte Seltene Krankheit der Tränenwege Septo-optic dysplasia spectrum Serpiginous choroiditis Sklerokornea, isolierte kongenitale Snowflake vitreoretinal degeneration Sorsby-Fundusdystrophie, pseudoinflammatorische Spasmus nutans Spastic ataxia-corneal dystrophy syndrome Spinocerebellar ataxia with oculomotor anomaly Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly Stargardt-Krankheit Stickler-Syndrom Stickler-Syndrom Typ 1 Stickler-Syndrom Typ 2 Stickler-Syndrom, autosomal-rezessives Strabismus, syndromale Formen Stromal corneal dystrophy Störung des sekretorischen Apparates der Tränenwege Superficial corneal dystrophy Superior limbic keratoconjunctivitis Sympathische Ophthalmie Syndrom der Foveahypoplasie mit Anomalie des Chiasma opticum und Dysgenesie des vorderen Augensegmentes Syndromic aniridia Syndromic cataract Syndromic corneal dystrophy Syndromic hyperopia Syndromic keratoconus Syndromic microphthalmia type 5 Syndromic microphthalmia-anophthalmia-coloboma Syndromic optic nerve hypoplasia Syndromic rod-cone dystrophy Syndromic telecanthus Systemic diseases with panuveitis Systemic diseases with posterior uveitis Systemische Krankheit mit anteriorer Uveitis Talgdrüsentumor, palpebraler Tarsal kink syndrome Temperature-sensitive oculocutaneous albinism type 1 Thiel-Behnke-Hornhautdystrophie Tolosa-Hunt syndrome Toxic maculopathy due to antimalarial drugs Triple A syndrome Tritanopie Trochlearislähmung, kongenitale Tumor, epidermaler palpebraler Tumor, palpebraler pigmentierter Unclassified familial retinal dystrophy Usher syndrome Usher syndrome type 1 Usher syndrome type 2 Usher syndrome type 3 Uveitis Uveitis, anteriore Uveitis, intermediäre Uveitis, nicht-infektiöse posteriore Uveitis, posteriore Uveitis, posteriore, infektiöse Form Vasoproliferative tumor of the retina Vernal keratoconjunctivitis Vitreoretinale Degeneration Vitreoretinopathie Vogt-Koyanagi-Harada disease WAGR-Syndrom Wagner disease X-chromosomale retikuläre Pigmentierungsstörung X-linked cone dysfunction syndrome with myopia X-linked recessive ocular albinism X-linked retinal dysplasia Åland Islands eye disease