SE-ATLAS

Uveitis Rare disorder with strabismus Early-onset anterior polar cataract Congenital stromal corneal dystrophy Posterior amorphous corneal dystrophy Meesmann corneal dystrophy Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Cryptophthalmia Hereditary retinoblastoma X-linked endothelial corneal dystrophy Chondroectodermal dysplasia with night blindness Okihiro syndrome Cancer-associated retinopathy Cogan syndrome Intermediate uveitis Pediatric-onset glaucoma of genetic origin Anterior uveitis Oculocutaneous albinism type 1 Norrie disease Oculofaciocardiodental syndrome Oculocutaneous albinism type 3 Aplasia of lacrimal and salivary glands Benign concentric annular macular dystrophy Usher syndrome type 1 Endophthalmitis Oculoauricular syndrome, Schorderet type Fundus pulverulentus IRVAN syndrome Isolated microphthalmia-anophthalmia-coloboma Fleck corneal dystrophy SRD5A3-CDG Rare disorder with ptosis Congenital malformation of the eyelid Leber hereditary optic neuropathy Rare palpebral disorder Idiopathic panuveitis Retinitis punctata albescens Bradyopsia Ligneous conjunctivitis Non-infectious anterior uveitis Blepharo-cheilo-odontic syndrome Oculocutaneous albinism type 2 Revesz syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Idiopathic macular telangiectasia type 1 Coats disease Hypomyelination-congenital cataract syndrome Coralliform cataract Corneal endotheliitis Posterior polymorphous corneal dystrophy Epithelial basement membrane dystrophy Knobloch syndrome X-linked reticulate pigmentary disorder Eyelid border anomaly Spasmus nutans X-linked recessive ocular albinism Phacoanaphylactic uveitis Central areolar choroidal dystrophy Isolated distichiasis Oculocutaneous albinism type 4 Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Septo-optic dysplasia spectrum Morning glory disc anomaly Retinal macular dystrophy type 2 Familial retinal arterial macroaneurysm Serpiginous choroiditis Stickler syndrome type 1 Congenital microcoria Syndromic disorder with strabismus Tolosa-Hunt syndrome Rare ophthalmic disorder Cerulean cataract Congenital malformation of the eye with glaucoma as a major feature Central cloudy dystrophy of François Sorsby pseudoinflammatory fundus dystrophy Bothnia retinal dystrophy Lisch epithelial corneal dystrophy Familial drusen Colobomatous microphthalmia Congenital cornea plana Microblepharon-ablephara syndrome Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Fatty acid hydroxylase-associated neurodegeneration Congenital trigeminal anesthesia Oculocutaneous albinism Micro syndrome Oculocutaneous albinism type 1B Åland Islands eye disease Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Distal deletion 6p Congenital eyelid retraction Pellucid marginal degeneration Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome GAPO syndrome Familial exudative vitreoretinopathy Congenital cataract microcornea with corneal opacity Congenital hereditary endothelial dystrophy type I EEM syndrome Autosomal dominant optic atrophy plus syndrome Hypotrichosis with juvenile macular degeneration Late-onset retinal degeneration Early-onset X-linked optic atrophy Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome Gyrate atrophy of choroid and retina Coloboma of macula-brachydactyly type B syndrome Isolated congenital sclerocornea Bilateral acute depigmentation of the iris Primary early-onset glaucoma Congenital ectropion uveae Congenital primary aphakia Familial pterygium of the conjunctiva Microphthalmia, Lenz type Systemic diseases with panuveitis Rare oculomotor nerve disorder Vitreoretinopathy Retinal degeneration-nanophthalmos-glaucoma syndrome Early-onset partial cataract Anterior segment developmental anomaly without extraocular manifestations Early-onset nuclear cataract Goldmann-Favre syndrome Fuchs endothelial corneal dystrophy Stickler syndrome type 2 Gelatinous drop-like corneal dystrophy Retinoblastoma Vasoproliferative tumor of the retina Hereditary benign intraepithelial dyskeratosis North Carolina macular dystrophy Oligocone trichromacy Corneodermatoosseous syndrome PEHO syndrome Kandori fleck retina Isolated congenital megalocornea Ocular albinism Infectious epithelial keratitis Toxic maculopathy due to antimalarial drugs Paraneoplastic uveitis Eales disease WAGR syndrome Idiopathic posterior uveitis Autosomal recessive Stickler syndrome Blindness-scoliosis-arachnodactyly syndrome Coats plus syndrome Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome Corneal dystrophy-perceptive deafness syndrome Retinitis pigmentosa Blepharophimosis-ptosis-epicanthus inversus syndrome Autosomal dominant optic atrophy and peripheral neuropathy Cystoid macular dystrophy Aniridia-renal agenesis-psychomotor retardation syndrome Sympathetic ophthalmia Dermochondrocorneal dystrophy X-linked corneal dermoid Non-infectious posterior uveitis Aceruloplasminemia MMEP syndrome Moebius syndrome Muir-Torre syndrome Epithelial recurrent erosion dystrophy Supranuclear eye movement disorder Lens position anomaly Total early-onset cataract Juvenile glaucoma Rare isolated myopia Thiel-Behnke corneal dystrophy Rare disorder of the lacrimal apparatus Coloboma of eye lens Juvenile cataract-microcornea-renal glucosuria syndrome Coloboma of choroid and retina X-linked retinoschisis Rare eyelid malposition disorder Bardet-Biedl syndrome Congenital hereditary endothelial dystrophy type II Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome Okihiro syndrome due to 20q13 microdeletion Aniridia-cerebellar ataxia-intellectual disability syndrome Achromatopsia Fuchs heterochromic iridocyclitis Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome Early-onset non-syndromic cataract MORM syndrome Oculocutaneous albinism type 7 Fundus albipunctatus Cataract-glaucoma syndrome Congenital trochlear nerve palsy Optic atrophy-intellectual disability syndrome Birdshot chorioretinopathy 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 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 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 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 Axenfeld anomaly Reis-Bücklers corneal dystrophy Coloboma of iris Pigmented paravenous retinochoroidal atrophy Microspherophakia-metaphyseal dysplasia syndrome Aniridia-intellectual disability syndrome Epiblepharon Systemic diseases with posterior uveitis Oculocutaneous albinism type 6 Ocular albinism with late-onset sensorineural deafness Duane retraction syndrome Atopic keratoconjunctivitis Cerebroretinal vasculopathy 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 Microphthalmia-anophthalmia-coloboma 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 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 Microcornea-glaucoma-absent frontal sinuses syndrome Panuveitis Hermansky-Pudlak syndrome due to AP-3 deficiency Cataract-microcornea syndrome Syndromic oculocutaneous albinism 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 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 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 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 Axenfeld-Rieger syndrome 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 Syndrome de microphtalmie-atrophie cérébrale Syndrome irido-cornéo-endothélial Télangiectasie maculaire idiopathique type 3 Uvéite postérieure Dystrophie tachetée simulant le fundus flavimaculatus Dystrophie maculaire vitelliforme de Best Dystrophie cornéenne syndromique Communication artérioveineuse rétinienne congénitale Maladies systémiques avec uvéite antérieure Dystrophie cornéenne maculaire Hypoplasie syndromique du nerf optique Glaucome néovasculaire Conjonctivite gonococcique Syndrome d'Okihiro dû à une mutation ponctuelle Syndrome d'atrophie optique-cataracte autosomique dominante Aniridie isolée Dégénérescence choriorétinienne péripapillaire hélicoïdale Malformation capillaire de la rétine Microphtalmie avec défauts linéaires cutanés Maladie de Bietti Atrophie optique autosomique récessive type OPA7 Atrophie bifocale choriorétinienne progressive Microphtalmie-anophtalmie-colobome syndromique Albinisme oculocutané type 1A Monochromatisme à cônes bleus Paralysie horizontale du regard avec scoliose progressive Rétinoblastome non héréditaire Alacrymie congénitale isolée Syndrome d'anomalie des cônes avec myopie lié à l'X Syndrome d'anophtalmie/microphtalmie-atrésie de l'oesophage Anomalie de Rieger Kératite stromale à herpes simplex Syndrome d'ablépharie-macrostomie Syndrome triple A Maladie de Leber plus Syndrome d'Usher Dystrophie réticulée de l'épithélium pigmentaire rétinien Cataracte suturale précoce Dystrophie cornéenne postérieure Maladie rare avec atteinte conjonctivale comme manifestation majeure Apraxie oculomotrice type Cogan Syndrome EDICT Télécanthus syndromique Rétine tachetée familiale bénigne Pemphigoïde oculaire cicatricielle Vitréo-rétino-choroïdopathie autosomique dominante Euryblépharon Amylose AGel