SE-ATLAS

Hereditary retinoblastoma Rare disorder with strabismus Early-onset anterior polar cataract Posterior amorphous corneal dystrophy Congenital stromal corneal dystrophy Meesmann corneal dystrophy Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Intermediate uveitis Cogan syndrome X-linked endothelial corneal dystrophy Okihiro syndrome Chondroectodermal dysplasia with night blindness Cancer-associated retinopathy Cryptophthalmia Oculocutaneous albinism type 1 Anterior uveitis Pediatric-onset glaucoma of genetic origin Aplasia of lacrimal and salivary glands Oculofaciocardiodental syndrome Norrie disease Uveitis Oculocutaneous albinism type 3 Usher syndrome type 1 Benign concentric annular macular dystrophy Fundus pulverulentus Oculoauricular syndrome, Schorderet type IRVAN syndrome Fleck corneal dystrophy Isolated microphthalmia-anophthalmia-coloboma Endophthalmitis Leber hereditary optic neuropathy Bradyopsia SRD5A3-CDG Congenital malformation of the eyelid Retinitis punctata albescens Idiopathic panuveitis Rare disorder with ptosis Ligneous conjunctivitis Non-infectious anterior uveitis Revesz syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Oculocutaneous albinism type 2 Idiopathic macular telangiectasia type 1 Blepharo-cheilo-odontic syndrome Knobloch syndrome Coralliform cataract Stickler syndrome type 1 Posterior polymorphous corneal dystrophy Coats disease Epithelial basement membrane dystrophy X-linked reticulate pigmentary disorder Phacoanaphylactic uveitis Central areolar choroidal dystrophy Spasmus nutans Hypomyelination-congenital cataract syndrome X-linked recessive ocular albinism Isolated distichiasis Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Morning glory disc anomaly Oculocutaneous albinism type 4 Serpiginous choroiditis Septo-optic dysplasia spectrum Eyelid border anomaly Familial retinal arterial macroaneurysm Retinal macular dystrophy type 2 Syndromic disorder with strabismus Congenital microcoria Tolosa-Hunt syndrome Cerulean cataract Central cloudy dystrophy of François Bothnia retinal dystrophy Lisch epithelial corneal dystrophy Colobomatous microphthalmia Oculocutaneous albinism Micro syndrome Sorsby pseudoinflammatory fundus dystrophy Fatty acid hydroxylase-associated neurodegeneration Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Congenital trigeminal anesthesia Familial drusen Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Oculocutaneous albinism type 1B GAPO syndrome Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome Congenital eyelid retraction Congenital cornea plana Microblepharon-ablephara syndrome Åland Islands eye disease Distal deletion 6p Pellucid marginal degeneration Congenital malformation of the eye with glaucoma as a major feature Hypotrichosis with juvenile macular degeneration Autosomal dominant optic atrophy plus syndrome Familial exudative vitreoretinopathy Rare ophthalmic disorder Congenital cataract microcornea with corneal opacity Anterior segment developmental anomaly without extraocular manifestations EEM syndrome Late-onset retinal degeneration Coloboma of macula-brachydactyly type B syndrome Early-onset X-linked optic atrophy Bilateral acute depigmentation of the iris Gyrate atrophy of choroid and retina Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome Congenital ectropion uveae Primary early-onset glaucoma Congenital primary aphakia Rare oculomotor nerve disorder Systemic diseases with panuveitis Microphthalmia, Lenz type Vitreoretinopathy Early-onset partial cataract Retinal degeneration-nanophthalmos-glaucoma syndrome Congenital hereditary endothelial dystrophy type I Familial pterygium of the conjunctiva Stickler syndrome type 2 Fuchs endothelial corneal dystrophy Oligocone trichromacy Goldmann-Favre syndrome Gelatinous drop-like corneal dystrophy Corneodermatoosseous syndrome Hereditary benign intraepithelial dyskeratosis Vasoproliferative tumor of the retina Retinoblastoma Isolated congenital megalocornea PEHO syndrome Kandori fleck retina North Carolina macular dystrophy Infectious epithelial keratitis Paraneoplastic uveitis Ocular albinism Isolated congenital sclerocornea Atopic keratoconjunctivitis Eales disease Toxic maculopathy due to antimalarial drugs Coats plus syndrome WAGR syndrome Idiopathic posterior uveitis Blindness-scoliosis-arachnodactyly syndrome Blepharophimosis-ptosis-epicanthus inversus syndrome Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome Autosomal recessive Stickler syndrome Early-onset nuclear cataract Dermochondrocorneal dystrophy Corneal dystrophy-perceptive deafness syndrome Retinitis pigmentosa Rare disorder of the lacrimal apparatus Rare isolated myopia Autosomal dominant optic atrophy and peripheral neuropathy Cystoid macular dystrophy 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 Total early-onset cataract Oguchi disease Juvenile glaucoma Thiel-Behnke corneal dystrophy Bardet-Biedl syndrome Coloboma of eye lens 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 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 Coloboma of choroid and retina Acute endophthalmitis Developmental defect of the eye Autosomal dominant rhegmatogenous retinal detachment Microphthalmia with brain and digit anomalies Renal coloboma syndrome Congenital ectropion Peters anomaly 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 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 Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome Peters plus syndrome 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 Macular coloboma-cleft palate-hallux valgus syndrome Coloboma of iris Systemic diseases with posterior uveitis Epiblepharon Aniridia-intellectual disability syndrome Ocular albinism with late-onset sensorineural deafness Microphthalmia-anophthalmia-coloboma Gardner syndrome Syndromic keratoconus Cerebroretinal vasculopathy Wagner disease Rare disorder with lens opacification Oculocutaneous albinism type 6 Duane retraction syndrome Color-vision disease Essential iris atrophy 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 Aniridia-absent patella syndrome Acute annular outer retinopathy Superior limbic keratoconjunctivitis Chronic endophthalmitis Cone dystrophy with supernormal rod response High myopia-sensorineural deafness syndrome Lacrimal drainage system anomaly Syndromic hyperopia Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Rare lens disease MRCS syndrome 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 Syndromic aniridia Butterfly-shaped pigment dystrophy Nanophthalmos Pulverulent cataract 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 Blepharoptosis-myopia-ectopia lentis syndrome Neuro-ophthalmological disease 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 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 Autosomal dominant optic atrophy and cataract Rare palpebral disorder Okihiro syndrome due to a point mutation Gonococcal conjunctivitis Progressive bifocal chorioretinal atrophy Syndromic corneal dystrophy Isolated aniridia Bietti crystalline dystrophy Autosomal recessive optic atrophy, OPA7 type 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 virus stromal keratitis Usher syndrome Anophthalmia/microphthalmia-esophageal atresia syndrome Ablepharon macrostomia syndrome Leber plus disease Reticular dystrophy of the retinal pigment epithelium Syndromic microphthalmia-anophthalmia-coloboma Triple A syndrome Early-onset sutural cataract Syndromic telecanthus EDICT syndrome Ocular motor apraxia, Cogan type Rare disorder with conjunctival involvement as a major feature Neovascular glaucoma Posterior corneal dystrophy Familial benign flecked retina Ocular cicatricial pemphigoid Autosomal dominant vitreoretinochoroidopathy Euryblepharon Infectious anterior uveitis AGel amyloidosis