SE-ATLAS

Congenital microcoria Sorsby pseudoinflammatory fundus dystrophy Disease predisposing to age-related macular degeneration Familial retinal arterial macroaneurysm Early-onset nuclear cataract Goniodysgenesis Fuchs endothelial corneal dystrophy Autosomal recessive Stickler syndrome Conjunctival tumor Gelatinous drop-like corneal dystrophy Isolated congenital megalocornea Oligocone trichromacy Benign tumor of palpebral epidermis Micro syndrome Minimal pigment oculocutaneous albinism type 1 Fatty acid hydroxylase-associated neurodegeneration Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Congenital cornea plana Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome GAPO syndrome Oculocutaneous albinism North Carolina macular dystrophy Severe early-childhood-onset retinal dystrophy Congenital cataract microcornea with corneal opacity Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome Stickler syndrome type 2 Autosomal dominant optic atrophy and peripheral neuropathy Familial exudative vitreoretinopathy Pigmentation disorder with eye involvement EEM syndrome Syndromic disorder with strabismus Unclassified primitive or secondary maculopathy Hypomyelination-congenital cataract syndrome Coralliform cataract Autosomal dominant optic atrophy plus syndrome Glaucoma associated with neural crest cell migration anomaly Posterior polymorphous corneal dystrophy Hypotrichosis with juvenile macular degeneration Fundus albipunctatus Pigmented conjunctival lesion Epithelial basement membrane dystrophy Central areolar choroidal dystrophy Palpebral epidermal tumor Eyelid border anomaly Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome Gyrate atrophy of choroid and retina Syndromic oculocutaneous albinism Coloboma of macula-brachydactyly type B syndrome Primary early-onset glaucoma Isolated distichiasis Okihiro syndrome due to 20q13 microdeletion Intellectual disability-alacrima-achalasia syndrome X-linked reticulate pigmentary disorder Microphthalmia, Lenz type Oculocutaneous albinism type 4 Stickler syndrome type 1 Early-onset posterior polar cataract Corneodysgenesis Congenital glaucoma Retinal degeneration-nanophthalmos-glaucoma syndrome Rare refraction anomaly Subepithelial mucinous corneal dystrophy Coloboma of choroid and retina Fuchs heterochromic iridocyclitis Familial pterygium of the conjunctiva Endophthalmitis Malignant tumor of palpebral epidermis Goldmann-Favre syndrome Rare eyelid malposition disorder Corneodermatoosseous syndrome Infectious posterior uveitis PEHO syndrome Retinoblastoma Congenital primary aphakia Juvenile cataract-microcornea-renal glucosuria syndrome Congenital ectropion uveae Acute zonal occult outer retinopathy Early-onset non-syndromic cataract Eales disease Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Oculoauricular syndrome, Schorderet type Congenital trochlear nerve palsy Idiopathic linear interstitial keratitis MORM syndrome WAGR syndrome Ocular coloboma Congenital vitreoretinal dysplasia Lens size anomaly Vitreoretinopathy Early-onset partial cataract Anterior segment developmental anomaly without extraocular manifestations Congenital hereditary endothelial dystrophy type I Retinitis pigmentosa Corneal dystrophy-perceptive deafness syndrome Bulbar conjunctival dermoid or conjunctival dermolipoma Late-onset retinal degeneration Blepharophimosis-ptosis-epicanthus inversus syndrome Precancerous lesion of palpebral epidermis Progressive retinal dystrophy due to retinol transport defect Early-onset X-linked optic atrophy Posterior uveitis Aniridia-renal agenesis-psychomotor retardation syndrome Isolated congenital sclerocornea Systemic diseases with anterior uveitis MMEP syndrome Kandori fleck retina X-linked corneal dermoid Bilateral acute depigmentation of the iris Keratoconus Aceruloplasminemia Oculocutaneous albinism type 5 Moebius syndrome Muir-Torre syndrome Rare oculomotor nerve disorder Secretory apparatus of the lacrimal system anomaly Coloboma of iris Oguchi disease Pigmented palpebral tumor Achromatopsia Secondary entropion Congenital hereditary endothelial dystrophy type II X-linked retinoschisis Bardet-Biedl syndrome Epithelial recurrent erosion dystrophy Persistent placoid maculopathy Non-infectious posterior uveitis Tritanopia Aniridia-cerebellar ataxia-intellectual disability syndrome Macular coloboma-cleft palate-hallux valgus syndrome Isolated optic nerve hypoplasia/aplasia Oculomotor apraxia Hereditary vascular retinopathy Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Hereditary optic neuropathy HERNS syndrome Ectopia lentis-chorioretinal dystrophy-myopia syndrome Hermansky-Pudlak syndrome due to AP-3 deficiency Idiopathic macular telangiectasia type 1 Early-onset zonular cataract Secondary glaucoma due to a proliferation and differentiation anomaly Axenfeld anomaly Occult macular dystrophy Pigmented paravenous retinochoroidal atrophy Cataract-glaucoma syndrome Birdshot chorioretinopathy Reis-Bücklers corneal dystrophy Rare isolated myopia Thiel-Behnke corneal dystrophy Coloboma of eye lens Rare disorder of the lacrimal apparatus Ataxia-oculomotor apraxia type 1 Stargardt disease X-linked endothelial corneal dystrophy Cystoid macular dystrophy Palpebral sebaceous gland tumor Congenital entropion Aniridia Microphthalmia with brain and digit anomalies Renal coloboma syndrome Chondroectodermal dysplasia with night blindness Peters anomaly Dermochondrocorneal dystrophy Neurotrophic keratopathy Sympathetic ophthalmia Intermediate uveitis Hereditary hyperferritinemia-cataract syndrome Corneal dystrophy Choroideremia Anterior uveitis Isolated ectopia lentis Supranuclear eye movement disorder Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome Vitreoretinal degeneration Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Stickler syndrome Lens position anomaly Total early-onset cataract Corneoiridogoniodysgenesis Juvenile glaucoma Major induction processes eye anomaly Cone dystrophy with supernormal rod response SRD5A3-CDG MRCS syndrome Vogt-Koyanagi-Harada disease Peters plus syndrome Aniridia-ptosis-intellectual disability-familial obesity syndrome Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Idiopathic panuveitis Non-infectious anterior uveitis Infectious epithelial keratitis Snowflake vitreoretinal degeneration Anterior segment developmental anomaly Autosomal dominant optic atrophy, classic form Congenital stationary night blindness Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Rare lens disease Cogan-Reese syndrome Rare genetic eye disease Myopic macular degeneration X-linked retinal dysplasia Syndromic hyperopia Microspherophakia-metaphyseal dysplasia syndrome Granular corneal dystrophy type II Lacrimal drainage system anomaly Coloboma of eyelid Blindness-scoliosis-arachnodactyly syndrome Palpebral nevus Congenital ectropion Developmental defect of the eye Retinal macular dystrophy type 2 Aniridia-intellectual disability syndrome Cerebroretinal vasculopathy Hereditary retinoblastoma Atopic keratoconjunctivitis Ocular albinism with late-onset sensorineural deafness Spasmus nutans Duane retraction syndrome Oculocutaneous albinism type 1 Oculocutaneous or ocular albinism Behr syndrome Persistent hyperplastic primary vitreous Wagner disease Autosomal dominant optic atrophy Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Lens shape anomaly Microcornea-corectopia-macular hypoplasia syndrome Rare disease with glaucoma as a major feature Chandler syndrome Rare hyperopia and astigmatism Granular corneal dystrophy type I Congenital alacrima Coloboma of macula Palpebral lentiginosis 3-methylglutaconic aciduria type 3 Idiopathic anterior uveitis Vasoproliferative tumor of the retina Chronic endophthalmitis Tarsal kink syndrome Hereditary benign intraepithelial dyskeratosis Rare acquired eye disease Microphthalmia-ankyloblepharon-intellectual disability syndrome Aniridia-absent patella syndrome Herpes simplex virus stromal keratitis Pre-Descemet corneal dystrophy Autosomal recessive optic atrophy, OPA7 type Spinocerebellar ataxia with oculomotor anomaly Nervous system anomaly with eye involvement Isolated cryptophthalmia Color-vision disease Syndromic cataract Idiopathic uveal effusion syndrome Congenital Horner syndrome Microcornea-glaucoma-absent frontal sinuses syndrome Familial congenital palsy of trochlear nerve Palpebral piliary tumor Epicanthal fold Progressive cone dystrophy Alström syndrome Panuveitis Oculocutaneous albinism type 6 Epiblepharon Cataract-microcornea syndrome Nanophthalmos Pigmentation disorder with eye involvement, excluding albinism Abnormal eye movements Cone rod dystrophy Gardner syndrome Okihiro syndrome due to a point mutation Genetic vitreous-retinal disease Rare disorder with lens opacification Superior limbic keratoconjunctivitis Syndromic keratoconus Essential iris atrophy Dyssegmental dysplasia-glaucoma syndrome Lattice corneal dystrophy type I Systemic diseases with panuveitis Coloboma of optic disc Syndromic microphthalmia-anophthalmia-coloboma Vernal keratoconjunctivitis Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Canthal anomaly Isolated aniridia Microphthalmia-anophthalmia-coloboma Leber congenital amaurosis Syndromic microphthalmia type 5 Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome Coats plus syndrome Autosomal recessive bestrophinopathy Blepharoptosis-myopia-ectopia lentis syndrome Leber plus disease Reticular dystrophy of the retinal pigment epithelium Syndromic rod-cone dystrophy Anophthalmia/microphthalmia-esophageal atresia syndrome Butterfly-shaped pigment dystrophy Spastic ataxia-corneal dystrophy syndrome AGel amyloidosis Stromal corneal dystrophy Pulverulent cataract Schnyder corneal dystrophy Palpebral tumor with a vascular malformation Syndromic telecanthus Toxic maculopathy due to antimalarial drugs Rare eye disease due to a differentiation anomaly Rare inflammatory eye disease Ocular cicatricial pemphigoid Matthew-Wood syndrome Axenfeld-Rieger syndrome Paraneoplastic uveitis Rieger anomaly Optic atrophy-intellectual disability syndrome Ocular albinism Idiopathic posterior uveitis Oculocutaneous albinism type 7 Euryblepharon Mitochondrial DNA-related progressive external ophthalmoplegia Isolated congenital ectropion Amaurosis-hypertrichosis syndrome Autosomal dominant rhegmatogenous retinal detachment Usher syndrome type 2 Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly Autosomal dominant keratitis Best vitelliform macular dystrophy Autosomal recessive isolated optic atrophy Microphthalmia with linear skin defects syndrome Bietti crystalline dystrophy Polymicrogyria with optic nerve hypoplasia Syndromic optic nerve hypoplasia Adult-onset foveomacular vitelliform dystrophy Superficial corneal dystrophy Gonococcal conjunctivitis Isolated ankyloblepharon filiforme adnatum Mesenchymatous palpebral tumor Retinopathy of prematurity Syndromic aniridia Neuromyelitis optica spectrum disorder Familial flecked retinopathy Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome Blue cone monochromatism Pattern dystrophy Horizontal gaze palsy with progressive scoliosis Oculocutaneous albinism type 1A Fundus pulverulentus Ablepharon macrostomia syndrome IRVAN syndrome Fleck corneal dystrophy Triple A syndrome Benign concentric annular macular dystrophy Conjunctival hemangioma or hemolymphangioma Usher syndrome Conjunctival vascular anomaly Bradyopsia Ligneous conjunctivitis Inherited retinal disorder Kinetic eyelid anomaly Åland Islands eye disease Rare palpebral disorder Ocular motor apraxia, Cogan type EDICT syndrome Oculocutaneous albinism type 2 Pellucid marginal degeneration Usher syndrome type 1 Microphthalmia-brain atrophy syndrome Acute endophthalmitis Autosomal dominant vitreoretinochoroidopathy Iridocorneal endothelial syndrome Infectious anterior uveitis Neovascular glaucoma Familial benign flecked retina Multifocal pattern dystrophy simulating fundus flavimaculatus Unclassified familial retinal dystrophy Autosomal dominant neovascular inflammatory vitreoretinopathy Temperature-sensitive oculocutaneous albinism type 1 Syndromic corneal dystrophy Macular corneal dystrophy Posterior corneal dystrophy Early-onset sutural cataract Helicoid peripapillary chorioretinal degeneration Rare disorder with conjunctival involvement as a major feature Autosomal dominant optic atrophy and cataract Phacoanaphylactic uveitis Progressive bifocal chorioretinal atrophy Neurogenic palpebral tumor Idiopathic macular telangiectasia type 3 Rare palpebral, lacrimal system and conjunctival disease Cogan syndrome Congenital retinal arteriovenous communication Retinal capillary malformation Isolated congenital alacrima Non-hereditary retinoblastoma Pediatric-onset glaucoma of genetic origin X-linked cone dysfunction syndrome with myopia Norrie disease Rare ophthalmic disorder Essential strabismus Oculofaciocardiodental syndrome Colobomatous and areolar dystrophy Tolosa-Hunt syndrome Ocular albinism with congenital sensorineural deafness Grayson-Wilbrandt corneal dystrophy Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome Cerulean cataract Central cloudy dystrophy of François Congenital malformation of the eye with glaucoma as a major feature Conjunctival lymphangiectasia Congenital trigeminal anesthesia Lisch epithelial corneal dystrophy Colobomatous microphthalmia Palpebral tumor Neuro-ophthalmological disease Microblepharon-ablephara syndrome Cryptophthalmia Distal deletion 6p Leber hereditary optic neuropathy Isolated microphthalmia-anophthalmia-coloboma Familial drusen Retinitis punctata albescens Nuclear oculomotor paralysis Congenital eyelid retraction High myopia-sensorineural deafness syndrome Revesz syndrome Bothnia retinal dystrophy Oculocutaneous albinism type 1B Uveitis Knobloch syndrome Blepharo-cheilo-odontic syndrome Coats disease Corneal endotheliitis Rare disorder with strabismus Systemic diseases with posterior uveitis Okihiro syndrome Genetic macular dystrophy Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Early-onset anterior polar cataract Congenital stromal corneal dystrophy Posterior amorphous corneal dystrophy Conjunctival telangiectasia Meesmann corneal dystrophy Congenital upper palpebral retraction Rare disorder with ptosis Septo-optic dysplasia spectrum Cancer-associated retinopathy Peters anomaly-cataract syndrome X-linked recessive ocular albinism Congenital malformation of the eyelid Morning glory disc anomaly Usher syndrome type 3 Oculocutaneous albinism type 3 Acute annular outer retinopathy Aplasia of lacrimal and salivary glands Panuvéite infectieuse Choroïdite serpigineuse