SE-ATLAS

Retinoblastom, familiäres Strabismus mit Restriktionssyndrom, selten Makuladystrophie, genetisch bedingte Katarakt, anteriore polare, früh-beginnende Hornhautdystrophie, amorphe posteriore Hornhautdystrophie, stromale, kongenitale Meesmann-Hornhautdystrophie Retinale Vaskulopathie mit zerebraler Leukoenzephalopathie und systemischen Manifestationen Uveitis, intermediäre Cogan-Syndrom Endothel-Hornhautdystrophie, X-chromosomale Okihiro-Syndrom Chondroektodermale Dysplasie mit Nachtblindheit Retinopathie, karzinomassoziierte Kryptophthalmie Albinismus, okulokutaner, Typ 1 Unterlidretraktion, palpebrale, kongenitale Uveitis, anteriore Glaukom, genetisch bedingtes, mit Beginn im Kindesalter Telangiektasie, konjunktivale Tränen- und Speicheldrüsenaplasie Okulo-fazio-kardio-dentales Syndrom Norrie-Syndrom Uveitis Albinismus, okulokutaner, Typ 3 Usher-Syndrom Typ 1 Makuladystrophie, anuläre benigne konzentrische Fundus pulverulentus Okuloaurikuläres Syndrom Typ Schorderet IRVAN-Syndrom Fleckchen-Hornhautdystrophie Mikrophthalmie-Anophthalmie-Kolobom, isoliert Endophthalmitis Leber-Optikusneuropathie, hereditäre Bradyopsie Peters Anomalie-Katarakt-Syndrom SRD5A3-CDG Augenlid-Fehlbildung Netzhautdystrophie Retinitis punctata albescens Panuveitis, idiopathische Seltene Störung mit Ptosis Hämangiom/Hämolymphangiom, konjunktivales Konjunktivitis, lignöse Uveitis, anteriore, nicht-infektiöse Form Revesz-Syndrom Intraepitheliale korneale Dyskeratose-palmoplantare Hyperkeratose-laryngeale Dyskeratose-Syndrom Albinismus, okulokutaner, Typ 2 Idiopathische makuläre Teleangiektasie Typ 1 Blepharo-cheilo-dentales Syndrom Knobloch-Syndrom Katarakt, koralliforme Stickler-Syndrom Typ 1 Hornhautdystrophie, polymorphe posteriore Coats-Krankheit Basalmembrandystrophie, epitheliale X-chromosomale retikuläre Pigmentierungsstörung Uveitis, phakoanaphylaktische Aderhautdystrophie, areoläre zentrale Spasmus nutans Hypomyelinisierung - kongenitale Katarakt Albinismus, okulärer rezessiver X-chromosomaler Distichiasis, isolierte Mikrokornea-myopische chorioretinale Atrophie-Telekanthus-Syndrom Morning-Glory-Papille Albinismus, okulokutaner, Typ 4 Chorioditis, serpiginöse Septo-optische Dysplasie-Spektrum Augenlidkante, Anomalie der Tumor, epidermaler palpebraler Makroaneurysmen, arterielle retinale, familiäre Form Makuladystrophie, retinale, Typ 2 Pigmentierungsstörung mit assoziierter Augenbeteiligung Bindehautläsion, pigmentierte Strabismus, syndromale Formen Migrationsanomalie der Neuralleistenzellen mit Glaukom Mikrokorie, kongenitale Makulopathie, primäre oder sekundäre, sonstige Dystrophie, areoläre und kolobomatöse Tolosa-Hunt-Syndrom Katarakt, zölinblaue Zentral-wolkenförmige Dystrophie François Netzhautdystrophie Typ Bottnien Lisch-epitheliale Hornhautdystrophie Mikrophtalmie, kolobomatöse Albinismus, okulokutaner Mikro-Syndrom Sorsby-Fundusdystrophie, pseudoinflammatorische Fettsäure-Hydroxylase-assoziierte Neurodegeneration Im Kindesalter beginnende autosomal-rezessive Myopathie mit externer Ophtalmoplegie Trigeminusanästhesie, kongenitale Drusen, familiäre Netzhautdystrophie mit Dysfunktion der inneren Retina und Ganglienzellanomalien Albinismus, okulokutaner, Typ 1B GAPO-Syndrom Glaukom-Ektopia lentis-Mikrosphärophakie-steife Gelenke-Kleinwuchs-Syndrom Supranukleäre Blickparese Augenlidretraktion, kongenitale Cornea plana, kongenitale Mikroblepharon - Ablepharie Åland Island-Augenkrankheit Distale Deletion 6p Tumor, palpebraler Hornhautdegeneration, marginale pelluzide Lymphangiektasie, konjunktivale Glaucoma, secondary dysgenetic Hypotrichose - juvenile Makuladegeneration Optikusatrophie plus-Syndrom, autosomal-dominantes Retinopathie, exsudative familiäre Augenkrankheit, seltene Katarakt, kongenitale - Mikrokornea - Hornhauttrübung Strabismus, essentieller Dermoid/Dermolipom, konjunktivales Anomalie des vorderen Augensegmentes ohne extraokuläre Manifestationen EEM-Syndrom Netzhautdystrophie, spät beginnende Makula-Kolobom - Brachydaktylie Typ B Optikusatrophie, X-chromosomale, mit frühem Beginn Irisdepigmentierung, akute bilaterale Atrophia gyrata der Chorioidea und Retina Mikrotie-Augenkolobom-imperforierter nasolakrimaler Gang-Syndrom Ektropion uveae, kongenitales Glaukom, primäres Aphakie, kongenitale primäre Okulomotorische Lähmung Systemische Krankheit mit Panuveitis Mikrophthalmie Typ Lenz Vitreoretinopathie Katarakt, partielle, früh-beginnende Palpebrale Epidermis, präkanzeröse Läsion der Netzhautdegeneration-Nanophthalmus-Glaukom-Syndrom Endotheldystrophie, hereditäre kongenitale 1 Pterygium conjunctivae, familiäre Form Stickler-Syndrom Typ 2 Endotheliale Hornhautdystrophie Fuchs Oligocone-Trichromasie Goldmann-Favre-Syndrom Hornhautdystrophie, gelatinöse tropfenförmige Korneo-dermato-ossäres-Syndrom Hereditäre benigne intraepitheliale Dyskeratose Vasoproliferativer Tumor der Retina Retinoblastom Megalokornea, isolierte kongenitale PEHO-Syndrom Gefleckte Retina nach Kandori North-Carolina-Makuladystrophie Keratitis, epitheliale infektiöse Uveitis, paraneoplastische 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 Mesenchymatous palpebral tumor Progressive retinal dystrophy due to retinol transport defect Schnyder corneal dystrophy Neuromyelitis optica spectrum disorder Syndromic microphthalmia type 5 Cone rod dystrophy Stromal corneal dystrophy Leber congenital amaurosis Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Isolated ankyloblepharon filiforme adnatum Dyssegmental dysplasia-glaucoma syndrome Isolated congenital ectropion Retinopathy of prematurity Usher syndrome type 3 Intellectual disability-alacrima-achalasia syndrome Acute zonal occult outer retinopathy Microphthalmia-ankyloblepharon-intellectual disability syndrome Familial congenital palsy of trochlear nerve Pattern dystrophy Infectious posterior uveitis Epicanthal fold Spinocerebellar ataxia with oculomotor anomaly Blepharoptosis-myopia-ectopia lentis syndrome Neuro-ophthalmological disease Palpebral piliary tumor Autosomal recessive isolated optic atrophy Adult-onset foveomacular vitelliform dystrophy Minimal pigment oculocutaneous albinism type 1 Syndromic cataract Superficial corneal dystrophy Severe early-childhood-onset retinal dystrophy Spastic ataxia-corneal dystrophy syndrome Idiopathic uveal effusion syndrome Isolated cryptophthalmia Axenfeld-Rieger syndrome Idiopathic linear interstitial keratitis Congenital Horner syndrome Matthew-Wood syndrome Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Rare acquired eye disease Mitochondrial DNA-related progressive external ophthalmoplegia Corneal endotheliitis Amaurosis-hypertrichosis syndrome Tarsal kink syndrome Temperature-sensitive oculocutaneous albinism type 1 Iridocorneal endothelial syndrome Systemic diseases with anterior uveitis Autosomal dominant keratitis Microphthalmia-brain atrophy syndrome Multifocal pattern dystrophy simulating fundus flavimaculatus Idiopathic macular telangiectasia type 3 Congenital retinal arteriovenous communication Posterior uveitis Syndromic optic nerve hypoplasia Macular corneal dystrophy Best vitelliform macular dystrophy Retinal capillary malformation Microphthalmia with linear skin defects syndrome Rare palpebral, lacrimal system and conjunctival disease Autosomal dominant optic atrophy and cataract Rare palpebral disorder Okihiro syndrome due to a point mutation Gonococcal conjunctivitis Kinetic eyelid anomaly Progressive bifocal chorioretinal atrophy Conjunctival vascular anomaly Syndromic corneal dystrophy Isolated aniridia Bietti crystalline dystrophy Autosomal recessive optic atrophy, OPA7 type Unclassified familial retinal dystrophy Horizontal gaze palsy with progressive scoliosis Blue cone monochromatism Oculocutaneous albinism type 1A Isolated congenital alacrima Helicoid peripapillary chorioretinal degeneration X-linked cone dysfunction syndrome with myopia Non-hereditary retinoblastoma Rieger anomaly 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