SE-ATLAS

3-methylglutaconic aciduria type 3 Ablepharon-Makrostomie-Syndrom Aceruloplasminemia Achromatopsia Acute zonal occult outer retinopathy Adulte foveomakuläre vitelliforme Dystrophie Agel-Amyloidose Alakrimie, isolierte kongenitale Albinismus, okulokutaner, Typ 1, temperaturempfindlicher Albinismus, okulokutaner, Typ 1A Albinismus, okulokutaner, Typ 1B Albinismus, okulokutaner, Typ 2 Albinismus, okulokutaner, Typ 3 Albinismus, okulokutaner, Typ 6 Albinismus, okulokutaner, Typ 7 Albinismus, okulärer Albinismus, okulärer rezessiver X-chromosomaler Alström-Syndrom Amaurose-Hypertrichose-Syndrom Amaurosis congenita Leber Aniridia Aniridia-absent patella syndrome Aniridia-cerebellar ataxia-intellectual disability syndrome Aniridia-intellectual disability syndrome Aniridia-ptosis-intellectual disability-familial obesity syndrome Aniridia-renal agenesis-psychomotor retardation syndrome Aniridie, isolierte Aniridie, syndromale Ankyloblepharon filiforme adnatum, isoliertes Anomalie des Nervensystems mit Augenkrankheit Anophtalmie-Mikrophtalmie-Syndrom Anophthalmie/Mikrophthalmie - Ösophagusatresie Anterior segment developmental anomaly Anterior segment developmental anomaly without extraocular manifestations Anterior uveitis Apraxie, okulomotorische, Typ Cogan Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Ataxia-oculomotor apraxia type 1 Ataxie, spinozerebelläre, mit okulomotorischer Anomalie Atopic keratoconjunctivitis Atrophie, bifokale chorioretinale progressive Augenbewegungsstörung Augenkrankheit bei Differenzierungsanomalie Augenkrankheit, seltene Augenlid-Fehlbildung Augenlidanomalie, kinetische Augenlidretraktion, kongenitale Autosomal dominant optic atrophy Autosomal dominant optic atrophy and peripheral neuropathy Autosomal dominant optic atrophy plus syndrome Autosomal dominant optic atrophy, classic form Autosomal recessive Stickler syndrome Axenfeld anomaly Axenfeld-Rieger-Syndrom Bardet-Biedl syndrome Behr syndrome Benign tumor of palpebral epidermis Best vitelliforme Makuladegeneration Bestrophinopathie, autosomal-rezessive Bietti-Kristalldystrophie Bilateral acute depigmentation of the iris Bindehautanomlie, vaskuläre Bindehautkrankheit, seltene Birdshot chorioretinopathy Blauzapfenmonochromasie Blepharo-cheilo-dentales Syndrom Blepharophimosis-ptosis-epicanthus inversus syndrome Blepharoptose - Myopie - Linsenektopie Blindness-scoliosis-arachnodactyly syndrome Bradyopsie Bulbar conjunctival dermoid or conjunctival dermolipoma Cataract-glaucoma syndrome Central areolar choroidal dystrophy Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Cerebroretinal vasculopathy Chandler syndrome Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Chondroectodermal dysplasia with night blindness Chorioditis, serpiginöse Chorioretinale Degeneration, helikoid-peripapilläre Choroideremia Chronic endophthalmitis Coats plus-Syndrom Coats-Krankheit Cogan-Reese syndrome Cogan-Syndrom Coloboma of choroid and retina Coloboma of eye lens Coloboma of eyelid Coloboma of iris Coloboma of macula Coloboma of macula-brachydactyly type B syndrome Cone dystrophy with supernormal rod response Congenital alacrima Congenital cataract microcornea with corneal opacity Congenital cornea plana Congenital ectropion Congenital ectropion uveae Congenital entropion Congenital glaucoma Congenital hereditary endothelial dystrophy type I Congenital hereditary endothelial dystrophy type II Congenital microcoria Congenital primary aphakia Congenital stationary night blindness Congenital trochlear nerve palsy Congenital vitreoretinal dysplasia Conjunctival tumor Coralliform cataract Corneal dystrophy Corneal dystrophy-perceptive deafness syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Corneodermatoosseous syndrome Corneodysgenesis Corneoiridogoniodysgenesis Cystoid macular dystrophy Dermochondrocorneal dystrophy Developmental defect of the eye Disease predisposing to age-related macular degeneration Distale Deletion 6p Drusen, familiäre Duane retraction syndrome Dysplasie, dyssegmentale - Glaukom Dystrophie, areoläre und kolobomatöse EDICT-Syndrom EEM syndrome Eales disease Early-onset X-linked optic atrophy Early-onset non-syndromic cataract Early-onset nuclear cataract Early-onset partial cataract Early-onset posterior polar cataract Early-onset zonular cataract Ectopia lentis-chorioretinal dystrophy-myopia syndrome Ektropion, isoliertes kongenitales Endophthalmitis Endophthalmitis, akute Endotheliitis Epiblepharon Epikanthus lateralis/medialis Epithelial basement membrane dystrophy Epithelial recurrent erosion dystrophy Euryblepharon Eyelid border anomaly Familial exudative vitreoretinopathy Familial pterygium of the conjunctiva Familial retinal arterial macroaneurysm Farbsehstörung Fatty acid hydroxylase-associated neurodegeneration Fleckchen-Hornhautdystrophie Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome Früh beginnende progressive Neurodegeneration-Blindheit-Ataxie-Spastik-Syndrom Frühgeborenen-Retinopathie Frühjahrskonjunktivitis Fuchs endothelial corneal dystrophy Fuchs heterochromic iridocyclitis Fundus albipunctatus Fundus pulverulentus GAPO syndrome Gardner-Syndrom Gefleckte Retina, benigne familiäre Gelatinous drop-like corneal dystrophy Glaucoma associated with neural crest cell migration anomaly Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Glaucoma, secondary dysgenetic Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome Glaukom, genetisch bedingtes, mit Beginn im Kindesalter Glaukom, neovaskuläres Goldmann-Favre syndrome Goniodysgenesis Gonokokkenkonjunktivitis Granular corneal dystrophy type I Granular corneal dystrophy type II Grayson-Wilbrandt-Hornhautdystrophie Gyrate atrophy of choroid and retina HERNS syndrome Hereditary benign intraepithelial dyskeratosis Hereditary hyperferritinemia-cataract syndrome Hereditary optic neuropathy Hereditary retinoblastoma Hereditary vascular retinopathy Hermansky-Pudlak syndrome due to AP-3 deficiency Herpes simplex virus stromal keratitis Hochgradige Myopie-sensorineurale Schwerhörigkeit-Syndrom Horizontale Blicklähmung mit progredienter Skoliose Horner-Syndrom, kongenitales Hornhautdegeneration, marginale pelluzide Hornhautdystrophie, amorphe posteriore Hornhautdystrophie, gittrige, Typ 1 Hornhautdystrophie, makuläre Hornhautdystrophie, posteriore Hornhautdystrophie, stromale Hornhautdystrophie, stromale, kongenitale Hornhautdystrophie, superfizielle Hornhautdystrophie, syndromale Hypomyelination-congenital cataract syndrome Hypotrichosis with juvenile macular degeneration Hämangiom/Hämolymphangiom, konjunktivales IRVAN-Syndrom Idiopathic anterior uveitis Idiopathic linear interstitial keratitis Idiopathic macular telangiectasia type 1 Idiopathic panuveitis Idiopathische makuläre Teleangiektasie Typ 3 Infectious epithelial keratitis Infectious posterior uveitis Intellectual disability-alacrima-achalasia syndrome Intermediate uveitis Iridokorneales endotheliales Syndrom Irisatrophie, essentielle Isolated congenital megalocornea Isolated congenital sclerocornea Isolated distichiasis Isolated ectopia lentis Isolated optic nerve hypoplasia/aplasia Juvenile cataract-microcornea-renal glucosuria syndrome Juvenile glaucoma Kandori fleck retina Katarakt, anteriore polare, früh-beginnende Katarakt, pulverförmige Katarakt, seltene Katarakt, suturale, früh-beginnende Katarakt, syndromale Katarakt, zölinblaue Katarakt-Mikrokornea-Syndrom Keratitis, autosomal-dominante Keratoconus Keratokonjunktivitis, limbische superiore Keratokonus, syndromaler Knobloch-Syndrom Kolobomatöse Mikrophtalmie-Adipositas-Hypogenitalismus-Intelligenzminderung-Syndrom Konjunktivitis, lignöse Kryptophthalmie Kryptophthalmie, isolierte Lacrimal drainage system anomaly Late-onset retinal degeneration Leber plus-Krankheit Leber-Optikusneuropathie, hereditäre Lens position anomaly Lens shape anomaly Lens size anomaly Lidwinkel-Anomalie Lisch-epitheliale Hornhautdystrophie Lymphangiektasie, konjunktivale MMEP syndrome MORM syndrome MRCS syndrome Macular coloboma-cleft palate-hallux valgus syndrome Major induction processes eye anomaly Makuladystrophie, anuläre benigne konzentrische Makuladystrophie, genetisch bedingte Makulopathie, toxische, durch anti-Malaria-Medikamente Malignant tumor of palpebral epidermis Matthew-Wood-Syndrom Meesmann-Hornhautdystrophie Micro syndrome Microcornea-corectopia-macular hypoplasia syndrome Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome Microphthalmia with brain and digit anomalies Microphthalmia, Lenz type Microphthalmia-ankyloblepharon-intellectual disability syndrome Microspherophakia-metaphyseal dysplasia syndrome Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome Mikroblepharon - Ablepharie Mikrokornea-Glaukom-fehlende Stirnhöhlen-Syndrom Mikrophtalmie, kolobomatöse Mikrophthalmie-Anophthalmie-Kolobom, isoliert Mikrophthalmie-Hirnatrophie-Syndrom Mikrophthalmie-Retinitis pigmentosa-Foveoschisis-Drusenpapille-Syndrom Mikrophthalmie-lineares Hautdefekt-Syndrom Minimal pigment oculocutaneous albinism type 1 Moebius syndrome Morning-Glory-Papille Muir-Torre syndrome Musterdystrophie, multifokale (vorgetäuschter Fundus flavimaculatus) Musterdystrophien des retinalen Pigmentepithels Myopic macular degeneration Nanophthalmie Netzhautablösung, rhegmatogene, autosomal-dominante Netzhautdystrophie Netzhautdystrophie Typ Bottnien Netzhautdystrophie des retinalen Pigmentepithels Netzhautdystrophie, hereditäre, sonstige Netzhautdystrophie-Sehnervödem-Splenomegalie-Anhidrose-Migräne-Kopfschmerz-Syndrom Neuro-ophthalmologische Krankheit Neuromyelitis-optica-Spektrum-Störung Neurotrophic keratopathy Non-infectious anterior uveitis Non-infectious posterior uveitis Norrie-Syndrom North Carolina macular dystrophy Occult macular dystrophy Ocular albinism with late-onset sensorineural deafness Ocular coloboma Oculoauricular syndrome, Schorderet type Oculocutaneous albinism Oculocutaneous albinism type 1 Oculocutaneous albinism type 4 Oculocutaneous albinism type 5 Oculocutaneous or ocular albinism Oculomotor apraxia Oguchi disease Okihiro syndrome due to 20q13 microdeletion Okihiro-Syndrom Okihiro-Syndrom durch Punktmutationen Okulo-fazio-kardio-dentales Syndrom Okulärer Albinismus mit kongenitaler sensorineuraler Schwerhörigkeit Oligocone trichromacy Ophthalmoplegie, chronische externe progressive, maternal-vererbte Optikusatrophie und Katarakt, autosomal-dominante Form Optikusatrophie, autosomal-rezessive, Typ 7 Optikusatrophie, isolierte, autosomal-rezessive Optikusatrophie-Intelligenzminderung-Syndrom PEHO syndrome Palpebral epidermal tumor Palpebral lentiginosis Palpebral nevus Palpebral sebaceous gland tumor Palpebraler Defekt, seltener Panuveitis Panuveitis, infektiöse Papillenkolobom Pemphigoid, okuläres vernarbendes Persistent hyperplastic primary vitreous Persistent placoid maculopathy Peters Anomalie-Katarakt-Syndrom Peters anomaly Peters plus syndrome Pigmentation disorder with eye involvement Pigmentdystrophie, schmetterlingsförmige Pigmented conjunctival lesion Pigmented palpebral tumor Pigmented paravenous retinochoroidal atrophy Pigmentierungsstörung mit Augenbeteiligung (exklusive Albinismus) Polymikrogyrie mit Sehnerv-Hypoplasie Posterior polymorphous corneal dystrophy Posterior uveitis Pre-Descemet corneal dystrophy Precancerous lesion of palpebral epidermis Primary early-onset glaucoma Primäre Hypomagnesiämie mit Hyperkalziurie, Nephrokalzinoseund schwerer Augenbeteiligung Progressive retinal dystrophy due to retinol transport defect Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Rare acquired eye disease Rare disease with glaucoma as a major feature Rare disorder of the lacrimal apparatus Rare eyelid malposition disorder Rare genetic eye disease Rare hyperopia and astigmatism Rare isolated myopia Rare lens disease Rare oculomotor nerve disorder Rare refraction anomaly Reis-Bücklers corneal dystrophy Renal coloboma syndrome Retinal degeneration-nanophthalmos-glaucoma syndrome Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Retinal macular dystrophy type 2 Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Retinale arteriovenöse Kommunikation, kongenitale Retinale kapilläre Fehlbildung Retinitis pigmentosa Retinitis pigmentosa, syndromale Retinitis punctata albescens Retinoblastom, unilaterales Retinoblastoma Retinopathie, akute äußere ringförmige Retinopathie, gefleckte, familiäre Form Retinopathie, karzinomassoziierte Revesz-Syndrom Rieger-Anomalie SRD5A3-CDG Schnyder-Hornhautdystrophie Secondary entropion Secondary glaucoma due to a proliferation and differentiation anomaly Secretory apparatus of the lacrimal system anomaly Sehnerv-Hypoplasie, syndromale Seltene Krankheiten des palpebralen, lakrimalen und konjunktivalen Systems Seltene Störung mit Ptosis Seltene inflammatorische Augenkrankheit Septo-optische Dysplasie-Spektrum Severe early-childhood-onset retinal dystrophy Snowflake vitreoretinal degeneration Sorsby pseudoinflammatory fundus dystrophy Spasmus nutans Spastische Ataxie - Hornhautdystrophie Spinozerebelläre Degeneration und spastische Paraparese mit okulomotorischer Anomalie Stargardt disease Stickler syndrome Stickler syndrome type 1 Stickler syndrome type 2 Strabismus mit Restriktionssyndrom, selten Strabismus, essentieller Subepithelial mucinous corneal dystrophy Supranuclear eye movement disorder Supranukleäre Blickparese Sympathetic ophthalmia Syndromale Mikrophthalmie Typ 5 Syndromales Mikrophthalmie-Anophthalmie-Kolobom Syndromic disorder with strabismus Syndromic hyperopia Syndromic oculocutaneous albinism Systemic diseases with anterior uveitis Systemische Krankheit mit Panuveitis Systemische Krankheit mit posteriorer Uveitis Tarsal kink syndrome Telangiektasie, konjunktivale Telekanthus Thiel-Behnke corneal dystrophy Tolosa-Hunt-Syndrom Total early-onset cataract Trigeminusanästhesie, kongenitale Triple-A-Syndrom Tritanopia Trochlearislähmung, kongenitale, familiäre Form Tränen- und Speicheldrüsenaplasie Tumor, mesenchymatöser palpebraler Tumor, neurogener palpebraler Tumor, palpebraler Tumor, palpebraler piliärer Tumor, palpebraler, mit vaskulärer Fehlbildung Unclassified primitive or secondary maculopathy Unterlidretraktion, palpebrale, kongenitale Usher-Syndrom Usher-Syndrom Typ 1 Usher-Syndrom Typ 2 Usher-Syndrom Typ 3 Uveales Effusions-Syndrom, idiopathisches Uveitis Uveitis, anteriore, infektiöse Form Uveitis, paraneoplastische Uveitis, phakoanaphylaktische Uveitis, posteriore, idiopathische Vasoproliferative tumor of the retina Vitreoretinal degeneration Vitreoretinale Krankheit, genetisch bedingte Vitreoretinochoroidopathie, autosomal-dominante Vitreoretinopathie, inflammatorische neovaskuläre, autosomal-dominante Vitreoretinopathy Vogt-Koyanagi-Harada disease WAGR syndrome Wagner disease X-linked corneal dermoid X-linked endothelial corneal dystrophy X-linked reticulate pigmentary disorder X-linked retinal dysplasia X-linked retinoschisis Zapfen-Stäbchen-Dystrophie Zapfendystrophie, progressive Zapfendystrophie-Myopie-Syndrom, X-chromosomales Zentral-wolkenförmige Dystrophie François Åland Island-Augenkrankheit