SE-ATLAS

Uvéite Maladie rare avec strabisme Dystrophie maculaire génétique Cataracte polaire antérieure précoce Dystrophie cornéenne stromale congénitale Dystrophie cornéenne amorphe postérieure Télangiectasie de la conjonctive Dystrophie cornéenne de Meesmann Vasculopathie rétinienne avec leucoencéphalopathie cérébrale et manifestations systémiques Rétraction congénitale de la paupière supérieure Cryptophtalmie Rétinoblastome héréditaire Dystrophie cornéenne endothéliale liée à l'X Dysplasie chondroectodermique avec cécité nocturne Syndrome d'Okihiro Rétinopathie paranéoplasique Syndrome de Cogan Uvéite intermédiaire Glaucome à début pédiatrique d'origine génétique Uvéite antérieure Albinisme oculocutané type 1 Maladie de Norrie Syndrome oculo-facio-cardio-dentaire Albinisme oculocutané type 3 Aplasie des glandes salivaires et lacrymales Dystrophie maculaire annulaire concentrique bénigne Syndrome d'Usher type 1 Endophtalmie Syndrome oculo-auriculaire type Schorderet Fundus pulverulentus Syndrome IRVAN Microphtalmie-anophtalmie-colobome isolée Dystrophie cornéenne mouchetée Hémangiome ou hémolymphangiome de la conjonctive SRD5A3-CDG Maladie rare avec ptosis Syndrome d'anomalie de Peters-cataracte Malformation congénitale de la paupière Neuropathie optique héréditaire de Leber Maladie rare de la paupière Panuvéite idiopathique Rétinite ponctuée albescente Bradyopsie Conjonctivite ligneuse Maladie rétinienne héréditaire Uvéite antérieure non infectieuse Syndrome blépharo-cheilo-odontique Albinisme oculocutané type 2 Syndrome de Revesz Syndrome de dyskératose intraépithéliale cornéenne-kératodermie palmoplantaire-dyskératose laryngée Télangiectasie maculaire idiopathique type 1 Maladie de Coats Maculopathie primaire ou secondaire non classifiée Syndrome d'hypomyélinisation-cataracte congénitale Cataracte coralliforme Glaucome associé à une anomalie de la migration des cellules de la crête neurale Endothélite herpétique Dystrophie cornéenne postérieure polymorphe Lésion pigmentée de la conjonctive Dystrophie cornéenne de la membrane basale Syndrome de Knobloch Tumeur épidermique de la paupière Pigmentation réticulée liée au chromosome X Anomalie du bord libre de la paupière Spasmus nutans Albinisme oculaire récessif lié à l'X Uvéite phacoanaphylactique Dystrophie centrale aréolaire de la choroïde Distichiasis isolé Albinisme oculocutané type 4 Syndrome de microcornée-myopie avec atrophie choriorétinienne-télécanthus Septo-optische Dysplasie-Spektrum Morning-Glory-Papille Makuladystrophie, retinale, Typ 2 Makroaneurysmen, arterielle retinale, familiäre Form Chorioditis, serpiginöse Stickler-Syndrom Typ 1 Mikrokorie, kongenitale Pigmentierungsstörung mit assoziierter Augenbeteiligung Strabismus, syndromale Formen Strabismus, essentieller Tolosa-Hunt-Syndrom Dystrophie, areoläre und kolobomatöse Augenkrankheit, seltene Katarakt, zölinblaue Glaucoma, secondary dysgenetic Zentral-wolkenförmige Dystrophie François Sorsby-Fundusdystrophie, pseudoinflammatorische Lymphangiektasie, konjunktivale Netzhautdystrophie Typ Bottnien Lisch-epitheliale Hornhautdystrophie Drusen, familiäre Mikrophtalmie, kolobomatöse Tumor, palpebraler Cornea plana, kongenitale Mikroblepharon - Ablepharie Im Kindesalter beginnende autosomal-rezessive Myopathie mit externer Ophtalmoplegie Fettsäure-Hydroxylase-assoziierte Neurodegeneration Trigeminusanästhesie, kongenitale Albinismus, okulokutaner Mikro-Syndrom Albinismus, okulokutaner, Typ 1B Åland Island-Augenkrankheit Supranukleäre Blickparese Netzhautdystrophie mit Dysfunktion der inneren Retina und Ganglienzellanomalien Distale Deletion 6p Augenlidretraktion, kongenitale Hornhautdegeneration, marginale pelluzide Glaukom-Ektopia lentis-Mikrosphärophakie-steife Gelenke-Kleinwuchs-Syndrom GAPO-Syndrom Retinopathie, exsudative familiäre Katarakt, kongenitale - Mikrokornea - Hornhauttrübung Endotheldystrophie, hereditäre kongenitale 1 Dermoid/Dermolipom, konjunktivales EEM-Syndrom Optikusatrophie plus-Syndrom, autosomal-dominantes Palpebrale Epidermis, präkanzeröse Läsion der Hypotrichose - juvenile Makuladegeneration Netzhautdystrophie, spät beginnende Optikusatrophie, X-chromosomale, mit frühem Beginn Mikrotie-Augenkolobom-imperforierter nasolakrimaler Gang-Syndrom Atrophia gyrata der Chorioidea und Retina Makula-Kolobom - Brachydaktylie Typ B Sklerokornea, isolierte kongenitale Irisdepigmentierung, akute bilaterale Glaukom, primäres Ektropion uveae, kongenitales Aphakie, kongenitale primäre Pterygium conjunctivae, familiäre Form Mikrophthalmie Typ Lenz Systemische Krankheit mit Panuveitis Okulomotorische Lähmung Vitreoretinopathie Netzhautdegeneration-Nanophthalmus-Glaukom-Syndrom Katarakt, partielle, früh-beginnende Anomalie des vorderen Augensegmentes ohne extraokuläre Manifestationen Katarakt, nukleäre, früh-beginnende Goniodysgenesie Goldmann-Favre-Syndrom Endotheliale Hornhautdystrophie Fuchs Stickler-Syndrom Typ 2 Bindehauttumor Hornhautdystrophie, gelatinöse tropfenförmige Beninger Tumor der palpebralen Epidermis Retinoblastom Vasoproliferativer Tumor der Retina Hereditäre benigne intraepitheliale Dyskeratose North-Carolina-Makuladystrophie Oligocone-Trichromasie Korneo-dermato-ossäres-Syndrom PEHO-Syndrom Gefleckte Retina nach Kandori Megalokornea, isolierte kongenitale Albinismus, okulärer Keratitis, epitheliale infektiöse Makulopathie, toxische, durch anti-Malaria-Medikamente Uveitis, paraneoplastische Eales-Krankheit Kolobom des Auges WAGR-Syndrom Uveitis, posteriore, idiopathische Stickler-Syndrom, autosomal-rezessives Blindheit-Skoliose-Arachnodaktylie-Syndrom Makuladegeneration, myopische Coats plus-Syndrom Krankheit mit Prädisposition für altersabhängige Makuladegeneration Mikrokornea-Vorderer Lentikonus-persistierender primärer Vitreus-Kolobom-Syndrom Hornhautdystrophie - Schallempfindungs-Schwerhörigkeit Talgdrüsentumor, palpebraler Retinitis pigmentosa Entropium, kongenitales Blepharophimose-Ptosis-Epicanthus inversus-Syndrom Optikusatrophie und periphere Neuropathie, autosomal-dominant Makuladystrophie, zystoide Aniridie-Nierenagenesie-psychomotorische Retardierung-Syndrom Sympathische Ophthalmie Dystrophie, dermo-chondro-corneale Korneales Dermoid, X-chromosomales Uveitis, nicht-infektiöse posteriore Keratokonus Aceruloplasminämie MMEP-Syndrom Moebius-Syndrom Muir-Torre-Syndrom Rezidivierende Epithelerosions-Dystrophie Paralyse, okulomotorische supranukleäre Vitreoretinale Degeneration Linsenanomalie (Position) Katarakt, totale, früh-beginnende Corneoiridogoniodysgenesie Glaukom, juveniles Myopie, isolierte, seltene Thiel-Behnke-Hornhautdystrophie Seltene Krankheit der Tränenwege Linsenkolobom Juvenile Katarakt-Mikrokornea-renale Glukosurie-Syndrom Kolobom der Chorioidea und Retina Palpebrale Epidermis, maligner Tumor der Retinoschisis, X-chromosomale Augenlider, Fehlstellung der Bardet-Biedl-Syndrom Endotheldystrophie, hereditäre kongenitale, Typ II Syndrom der Foveahypoplasie mit Anomalie des Chiasma opticum und Dysgenesie des vorderen Augensegmentes Okihiro-Syndrom durch Monosomie 20q13 Aniridie-zerebelläre Ataxie-Intelligenzminderung-Syndrom Achromatopsie Fuchs Heterochromie-Iridozyklitis Kolobomatöse Mikrophtalmie-Adipositas-Hypogenitalismus-Intelligenzminderung-Syndrom Katarakt, nicht-syndromale, kongenitale MORM-Syndrom Albinismus, okulokutaner, Typ 7 Fundus albipunctatus Katarakt-Glaukom-Syndrom Trochlearislähmung, kongenitale Optikusatrophie-Intelligenzminderung-Syndrom Dysplasie, vitreoretinale, kongenitale Chorioretinopathie Typ Birdshot Lens size anomaly Early-onset posterior polar cataract Corneodysgenesis Ataxia-oculomotor apraxia type 1 Congenital glaucoma Stargardt disease Rare refraction anomaly Subepithelial mucinous corneal dystrophy Ectopia lentis-chorioretinal dystrophy-myopia syndrome Acute endophthalmitis Aniridia Renal coloboma syndrome Microphthalmia with brain and digit anomalies Autosomal dominant rhegmatogenous retinal detachment Infectious anterior uveitis Peters anomaly Autosomal dominant neovascular inflammatory vitreoretinopathy Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Neurotrophic keratopathy Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome Oculocutaneous or ocular albinism Polymicrogyria with optic nerve hypoplasia Corneal dystrophy Autosomal dominant optic atrophy Choroideremia Lens shape anomaly Rare disease with glaucoma as a major feature Chandler syndrome Stickler syndrome Familial flecked retinopathy Rare hyperopia and astigmatism Granular corneal dystrophy type I Isolated ectopia lentis Congenital alacrima Coloboma of macula Persistent hyperplastic primary vitreous Hereditary hyperferritinemia-cataract syndrome 3-methylglutaconic aciduria type 3 Palpebral lentiginosis Congenital ectropion Developmental defect of the eye Autosomal recessive bestrophinopathy Grayson-Wilbrandt corneal dystrophy Oguchi disease Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome Peters plus syndrome Aniridia-ptosis-intellectual disability-familial obesity syndrome Tritanopia Vogt-Koyanagi-Harada disease Persistent placoid maculopathy Usher syndrome type 2 Occult macular dystrophy Congenital stationary night blindness Hereditary vascular retinopathy Oculomotor apraxia Macular coloboma-cleft palate-hallux valgus syndrome Hereditary optic neuropathy HERNS syndrome Early-onset zonular cataract X-linked retinal dysplasia Secondary glaucoma due to a proliferation and differentiation anomaly Axenfeld anomaly Reis-Bücklers corneal dystrophy Secretory apparatus of the lacrimal system anomaly Coloboma of iris Rare inflammatory eye disease Pigmented palpebral tumor Pigmented paravenous retinochoroidal atrophy Microspherophakia-metaphyseal dysplasia syndrome Secondary entropion Aniridia-intellectual disability syndrome Epiblepharon Systemic diseases with posterior uveitis Oculocutaneous albinism type 6 Ocular albinism with late-onset sensorineural deafness Nervous system anomaly with eye involvement Duane retraction syndrome Atopic keratoconjunctivitis Cerebroretinal vasculopathy Genetic vitreous-retinal disease Behr syndrome Superior limbic keratoconjunctivitis Wagner disease Rare disorder with lens opacification Essential iris atrophy Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Syndromic keratoconus Lattice corneal dystrophy type I Pre-Descemet corneal dystrophy Coloboma of optic disc Gardner syndrome Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Vernal keratoconjunctivitis Infectious panuveitis Canthal anomaly Microphthalmia-anophthalmia-coloboma Idiopathic anterior uveitis Microcornea-corectopia-macular hypoplasia syndrome Chronic endophthalmitis Acute annular outer retinopathy Cone dystrophy with supernormal rod response MRCS syndrome Aniridia-absent patella syndrome High myopia-sensorineural deafness syndrome Ocular albinism with congenital sensorineural deafness Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Pigmentation disorder with eye involvement, excluding albinism Abnormal eye movements Isolated optic nerve hypoplasia/aplasia Anterior segment developmental anomaly Autosomal dominant optic atrophy, classic form Rare genetic eye disease Rare lens disease Cogan-Reese syndrome Progressive cone dystrophy Syndromic hyperopia Granular corneal dystrophy type II Alström syndrome Lacrimal drainage system anomaly Coloboma of eyelid Snowflake vitreoretinal degeneration Palpebral nevus Microcornea-glaucoma-absent frontal sinuses syndrome Panuveitis Major induction processes eye anomaly Hermansky-Pudlak syndrome due to AP-3 deficiency Cataract-microcornea syndrome Syndromic oculocutaneous albinism Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly Nanophthalmos Butterfly-shaped pigment dystrophy Pulverulent cataract Stromal corneal dystrophy Progressive retinal dystrophy due to retinol transport defect Schnyder corneal dystrophy Cone rod dystrophy Superficial corneal dystrophy Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Syndromic microphthalmia type 5 Mesenchymatous palpebral tumor Neuromyelitis optica spectrum disorder Syndromic aniridia Leber congenital amaurosis Dyssegmental dysplasia-glaucoma syndrome Isolated ankyloblepharon filiforme adnatum Pattern dystrophy Oculocutaneous albinism type 5 Intellectual disability-alacrima-achalasia syndrome Usher syndrome type 3 Isolated congenital ectropion Retinopathy of prematurity Tarsal kink syndrome Rare acquired eye disease Acute zonal occult outer retinopathy Infectious posterior uveitis Microphthalmia-ankyloblepharon-intellectual disability syndrome Minimal pigment oculocutaneous albinism type 1 Neuro-ophthalmological disease Blepharoptosis-myopia-ectopia lentis syndrome Spinocerebellar ataxia with oculomotor anomaly Autosomal recessive isolated optic atrophy Adult-onset foveomacular vitelliform dystrophy Color-vision disease Idiopathic uveal effusion syndrome Syndromic cataract Severe early-childhood-onset retinal dystrophy Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Isolated cryptophthalmia Spastic ataxia-corneal dystrophy syndrome Palpebral piliary tumor Axenfeld-Rieger syndrome Epicanthal fold Congenital Horner syndrome Mitochondrial DNA-related progressive external ophthalmoplegia Amaurosis-hypertrichosis syndrome Familial congenital palsy of trochlear nerve Matthew-Wood syndrome Idiopathic linear interstitial keratitis Autosomal dominant keratitis Temperature-sensitive oculocutaneous albinism type 1 Microphthalmia-brain atrophy syndrome Iridocorneal endothelial syndrome Unclassified familial retinal dystrophy Idiopathic macular telangiectasia type 3 Posterior uveitis Multifocal pattern dystrophy simulating fundus flavimaculatus Best vitelliform macular dystrophy Syndromic corneal dystrophy Congenital retinal arteriovenous communication Systemic diseases with anterior uveitis Macular corneal dystrophy Conjunctival vascular anomaly Syndromic optic nerve hypoplasia Neovascular glaucoma Kinetic eyelid anomaly Neurogenic palpebral tumor Gonococcal conjunctivitis Okihiro syndrome due to a point mutation Autosomal dominant optic atrophy and cataract Isolated aniridia Helicoid peripapillary chorioretinal degeneration Retinal capillary malformation Rare palpebral, lacrimal system and conjunctival disease Microphthalmia with linear skin defects syndrome Bietti crystalline dystrophy Autosomal recessive optic atrophy, OPA7 type Progressive bifocal chorioretinal atrophy Syndromic microphthalmia-anophthalmia-coloboma Oculocutaneous albinism type 1A Blue cone monochromatism Horizontal gaze palsy with progressive scoliosis Non-hereditary retinoblastoma Isolated congenital alacrima X-linked cone dysfunction syndrome with myopia Anophthalmia/microphthalmia-esophageal atresia syndrome Rieger anomaly Herpes simplex virus stromal keratitis Ablepharon macrostomia syndrome Triple A syndrome Leber plus disease Syndromic rod-cone dystrophy Usher syndrome Reticular dystrophy of the retinal pigment epithelium Early-onset sutural cataract Posterior corneal dystrophy Rare disorder with conjunctival involvement as a major feature Ocular motor apraxia, Cogan type Palpebral tumor with a vascular malformation EDICT syndrome Syndromic telecanthus Familial benign flecked retina Rare eye disease due to a differentiation anomaly Ocular cicatricial pemphigoid Autosomal dominant vitreoretinochoroidopathy Euryblepharon AGel amyloidosis