SE-ATLAS

3-methylglutaconic aciduria type 3 AGel amyloidosis Abnormal eye movements Aceruloplasminemia Achromatopsia Acute zonal occult outer retinopathy Adult-onset foveomacular vitelliform dystrophy Alacrymie congénitale isolée Albinisme oculaire avec surdité neurosensorielle congénitale Albinisme oculaire récessif lié à l'X Albinisme oculocutané type 1 thermosensible Albinisme oculocutané type 1A Albinisme oculocutané type 1B Albinisme oculocutané type 2 Albinisme oculocutané type 3 Alström syndrome Amaurosis-hypertrichosis syndrome Anesthésie congénitale du nerf trijumeau Aniridia Aniridia-absent patella syndrome Aniridia-cerebellar ataxia-intellectual disability syndrome Aniridia-intellectual disability syndrome Aniridia-ptosis-intellectual disability-familial obesity syndrome Aniridia-renal agenesis-psychomotor retardation syndrome Aniridie syndromique Ankyloblépharon filiforme adnatum isolé Anomalie de la cinétique de la paupière Anomalie papillaire morning glory Anomalie vasculaire de la conjonctive Anophthalmia/microphthalmia-esophageal atresia syndrome Anterior segment developmental anomaly Anterior segment developmental anomaly without extraocular manifestations Anterior uveitis Aplasie des glandes salivaires et lacrymales Apraxie oculomotrice type Cogan Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Ataxia-oculomotor apraxia type 1 Atopic keratoconjunctivitis Atrophie bifocale choriorétinienne progressive Autosomal dominant keratitis Autosomal dominant optic atrophy Autosomal dominant optic atrophy and peripheral neuropathy Autosomal dominant optic atrophy plus syndrome Autosomal dominant optic atrophy, classic form Autosomal dominant rhegmatogenous retinal detachment Autosomal recessive Stickler syndrome Autosomal recessive bestrophinopathy Autosomal recessive isolated optic atrophy Autosomal recessive optic atrophy, OPA7 type Axenfeld anomaly Axenfeld-Rieger syndrome Bardet-Biedl syndrome Behr syndrome Benign tumor of palpebral epidermis Best vitelliform macular dystrophy Bietti crystalline dystrophy Bilateral acute depigmentation of the iris Birdshot chorioretinopathy Blepharophimosis-ptosis-epicanthus inversus syndrome Blepharoptosis-myopia-ectopia lentis syndrome Blindness-scoliosis-arachnodactyly syndrome Bradyopsie Bulbar conjunctival dermoid or conjunctival dermolipoma Butterfly-shaped pigment dystrophy Canthal anomaly Cataract-glaucoma syndrome Cataract-microcornea syndrome Cataracte céruléenne Cataracte polaire antérieure précoce Cataracte suturale précoce Central areolar choroidal dystrophy Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Cerebroretinal vasculopathy Chandler syndrome Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Chondroectodermal dysplasia with night blindness Choroideremia Choroïdite serpigineuse Chronic endophthalmitis Coats plus syndrome Cogan-Reese syndrome Coloboma of choroid and retina Coloboma of eye lens Coloboma of eyelid Coloboma of iris Coloboma of macula Coloboma of macula-brachydactyly type B syndrome Coloboma of optic disc Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome Color-vision disease Communication artérioveineuse rétinienne congénitale Cone dystrophy with supernormal rod response Cone rod dystrophy Congenital Horner syndrome Congenital alacrima Congenital cataract microcornea with corneal opacity Congenital cornea plana Congenital ectropion Congenital ectropion uveae Congenital entropion Congenital glaucoma Congenital hereditary endothelial dystrophy type I Congenital hereditary endothelial dystrophy type II Congenital microcoria Congenital primary aphakia Congenital stationary night blindness Congenital trochlear nerve palsy Congenital vitreoretinal dysplasia Conjonctivite gonococcique Conjonctivite ligneuse Conjunctival tumor Coralliform cataract Corneal dystrophy Corneal dystrophy-perceptive deafness syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Corneodermatoosseous syndrome Corneodysgenesis Corneoiridogoniodysgenesis Cryptophtalmie Cystoid macular dystrophy Dermochondrocorneal dystrophy Developmental defect of the eye Disease predisposing to age-related macular degeneration Drusen familiaux Duane retraction syndrome Dyssegmental dysplasia-glaucoma syndrome Dystrophie aréolaire et colobomateuse Dystrophie cornéenne amorphe postérieure Dystrophie cornéenne de Grayson-Wilbrandt Dystrophie cornéenne de Lisch Dystrophie cornéenne de Meesmann Dystrophie cornéenne maculaire Dystrophie cornéenne mouchetée Dystrophie cornéenne postérieure Dystrophie cornéenne stromale congénitale Dystrophie cornéenne syndromique Dystrophie maculaire annulaire concentrique bénigne Dystrophie maculaire génétique Dystrophie nuageuse centrale de François Dystrophie rétinenne syndromique non classifiée Dystrophie rétinienne type Bothnie Dystrophie tachetée simulant le fundus flavimaculatus Dégénérescence choriorétinienne péripapillaire hélicoïdale Dégénérescence marginale pellucide Délétion distale 6p EEM syndrome Eales disease Early-onset X-linked optic atrophy Early-onset non-syndromic cataract Early-onset nuclear cataract Early-onset partial cataract Early-onset posterior polar cataract Early-onset zonular cataract Ectopia lentis-chorioretinal dystrophy-myopia syndrome Endophtalmie aiguë Endophthalmitis Endothélite herpétique Epiblepharon Epicanthal fold Epithelial basement membrane dystrophy Epithelial recurrent erosion dystrophy Essential iris atrophy Euryblepharon Eyelid border anomaly Familial congenital palsy of trochlear nerve Familial exudative vitreoretinopathy Familial pterygium of the conjunctiva Familial retinal arterial macroaneurysm Fatty acid hydroxylase-associated neurodegeneration Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome Fuchs endothelial corneal dystrophy Fuchs heterochromic iridocyclitis Fundus albipunctatus Fundus pulverulentus GAPO syndrome Gardner syndrome Gelatinous drop-like corneal dystrophy Genetic vitreous-retinal disease Glaucoma associated with neural crest cell migration anomaly Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome Glaucome néovasculaire Glaucome à début pédiatrique d'origine génétique Goldmann-Favre syndrome Goniodysgenesis Granular corneal dystrophy type I Granular corneal dystrophy type II Gyrate atrophy of choroid and retina HERNS syndrome Hereditary benign intraepithelial dyskeratosis Hereditary hyperferritinemia-cataract syndrome Hereditary optic neuropathy Hereditary retinoblastoma Hereditary vascular retinopathy Hermansky-Pudlak syndrome due to AP-3 deficiency Herpes simplex virus stromal keratitis Hypomyelination-congenital cataract syndrome Hypotrichosis with juvenile macular degeneration Hémangiome ou hémolymphangiome de la conjonctive Idiopathic anterior uveitis Idiopathic linear interstitial keratitis Idiopathic macular telangiectasia type 1 Idiopathic panuveitis Idiopathic posterior uveitis Idiopathic uveal effusion syndrome Infectious epithelial keratitis Infectious posterior uveitis Intellectual disability-alacrima-achalasia syndrome Intermediate uveitis Isolated aniridia Isolated congenital ectropion Isolated congenital megalocornea Isolated congenital sclerocornea Isolated cryptophthalmia Isolated distichiasis Isolated ectopia lentis Isolated optic nerve hypoplasia/aplasia Juvenile cataract-microcornea-renal glucosuria syndrome Juvenile glaucoma Kandori fleck retina Keratoconus Lacrimal drainage system anomaly Late-onset retinal degeneration Lattice corneal dystrophy type I Leber congenital amaurosis Leber plus disease Lens position anomaly Lens shape anomaly Lens size anomaly Lymphangiectasie de la conjonctive MMEP syndrome MORM syndrome MRCS syndrome Macular coloboma-cleft palate-hallux valgus syndrome Major induction processes eye anomaly Maladie de Coats Maladie de Norrie Maladie neuro-ophtalmologique Maladie ophtalmique des îles Åland Maladie ophtalmique rare Maladie rare avec atteinte conjonctivale comme manifestation majeure Maladie rare avec ptosis Maladie rare avec strabisme Maladie rare de la paupière Maladie rare de la paupière, de l'appareil lacrymal et de la conjonctive Maladie rétinienne héréditaire Maladies systémiques avec uvéite postérieure Malformation capillaire de la rétine Malformation congénitale de l'oeil avec glaucome comme manifestation majeure Malformation congénitale de la paupière Malignant tumor of palpebral epidermis Matthew-Wood syndrome Micro syndrome Microblépharon-ablépharie Microcornea-corectopia-macular hypoplasia syndrome Microcornea-glaucoma-absent frontal sinuses syndrome Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome Microphtalmie colobomateuse Microphtalmie-anophtalmie-colobome isolée Microphthalmia with brain and digit anomalies Microphthalmia with linear skin defects syndrome Microphthalmia, Lenz type Microphthalmia-ankyloblepharon-intellectual disability syndrome Microphthalmia-anophthalmia-coloboma Microspherophakia-metaphyseal dysplasia syndrome Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome Minimal pigment oculocutaneous albinism type 1 Mitochondrial DNA-related progressive external ophthalmoplegia Moebius syndrome Monochromatisme à cônes bleus Muir-Torre syndrome Myopic macular degeneration Nanophthalmos Nervous system anomaly with eye involvement Neuromyélite optique Neuropathie optique héréditaire de Leber Neurotrophic keratopathy Non-infectious anterior uveitis Non-infectious posterior uveitis North Carolina macular dystrophy Occult macular dystrophy Ocular albinism Ocular albinism with late-onset sensorineural deafness Ocular cicatricial pemphigoid Ocular coloboma Oculoauricular syndrome, Schorderet type Oculocutaneous albinism Oculocutaneous albinism type 1 Oculocutaneous albinism type 4 Oculocutaneous albinism type 5 Oculocutaneous albinism type 6 Oculocutaneous albinism type 7 Oculocutaneous or ocular albinism Oculomotor apraxia Oguchi disease Okihiro syndrome due to 20q13 microdeletion Okihiro syndrome due to a point mutation Oligocone trichromacy Optic atrophy-intellectual disability syndrome PEHO syndrome Palpebral epidermal tumor Palpebral lentiginosis Palpebral nevus Palpebral piliary tumor Palpebral sebaceous gland tumor Palpebral tumor with a vascular malformation Panuveitis Panuvéite infectieuse Paralysie horizontale du regard avec scoliose progressive Paralysie oculomotrice nucléaire Paraneoplastic uveitis Pattern dystrophie Persistent hyperplastic primary vitreous Persistent placoid maculopathy Peters anomaly Peters plus syndrome Pigmentation disorder with eye involvement Pigmentation disorder with eye involvement, excluding albinism Pigmented conjunctival lesion Pigmented palpebral tumor Pigmented paravenous retinochoroidal atrophy Polymicrogyria with optic nerve hypoplasia Posterior polymorphous corneal dystrophy Posterior uveitis Pre-Descemet corneal dystrophy Precancerous lesion of palpebral epidermis Primary early-onset glaucoma Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Progressive cone dystrophy Progressive retinal dystrophy due to retinol transport defect Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Pulverulent cataract Rare acquired eye disease Rare disease with glaucoma as a major feature Rare disorder of the lacrimal apparatus Rare disorder with lens opacification Rare eye disease due to a differentiation anomaly Rare eyelid malposition disorder Rare genetic eye disease Rare hyperopia and astigmatism Rare inflammatory eye disease Rare isolated myopia Rare lens disease Rare oculomotor nerve disorder Rare refraction anomaly Reis-Bücklers corneal dystrophy Renal coloboma syndrome Reticular dystrophy of the retinal pigment epithelium Retinal degeneration-nanophthalmos-glaucoma syndrome Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Retinal macular dystrophy type 2 Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Retinitis pigmentosa Retinoblastoma Rieger anomaly Rétine tachetée familiale bénigne Rétinite ponctuée albescente Rétinoblastome non héréditaire Rétinopathie du prématuré Rétinopathie en tache familiale Rétinopathie externe annulaire aiguë Rétinopathie paranéoplasique Rétraction congénitale de la paupière supérieure Rétraction congénitale des paupières SRD5A3-CDG Schnyder corneal dystrophy Secondary entropion Secondary glaucoma due to a proliferation and differentiation anomaly Secretory apparatus of the lacrimal system anomaly Severe early-childhood-onset retinal dystrophy Snowflake vitreoretinal degeneration Sorsby pseudoinflammatory fundus dystrophy Spasmus nutans Spastic ataxia-corneal dystrophy syndrome Spectre de dysplasie septo-optique Spinocerebellar ataxia with oculomotor anomaly Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly Stargardt disease Stickler syndrome Stickler syndrome type 1 Stickler syndrome type 2 Strabisme essentiel Stromal corneal dystrophy Subepithelial mucinous corneal dystrophy Superficial corneal dystrophy Superior limbic keratoconjunctivitis Supranuclear eye movement disorder Sympathetic ophthalmia Syndrome EDICT Syndrome IRVAN Syndrome blépharo-cheilo-odontique Syndrome d'Okihiro Syndrome d'Usher Syndrome d'Usher type 1 Syndrome d'Usher type 3 Syndrome d'ablépharie-macrostomie Syndrome d'anomalie de Peters-cataracte Syndrome d'anomalie des cônes avec myopie lié à l'X Syndrome d'atrophie optique-cataracte autosomique dominante Syndrome de Cogan Syndrome de Knobloch Syndrome de Revesz Syndrome de Tolosa-Hunt Syndrome de dystrophie rétinienne-oedème du nerf optique-splénomégalie-anhidrose-céphalée migraineuse Syndrome de microphtalmie-atrophie cérébrale Syndrome de microphtalmie-rétinite pigmentaire-fovéoschisis-drusen de la papille optique Syndrome de myopie forte-surdité neurosensorielle Syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité Syndrome irido-cornéo-endothélial Syndrome oculo-facio-cardio-dentaire Syndrome triple A Syndromic cataract Syndromic disorder with strabismus Syndromic hyperopia Syndromic keratoconus Syndromic microphthalmia type 5 Syndromic microphthalmia-anophthalmia-coloboma Syndromic oculocutaneous albinism Syndromic optic nerve hypoplasia Syndromic rod-cone dystrophy Syndromic telecanthus Systemic diseases with anterior uveitis Systemic diseases with panuveitis Tarsal kink syndrome Thiel-Behnke corneal dystrophy Total early-onset cataract Toxic maculopathy due to antimalarial drugs Tritanopia Tumeur de la paupière Tumeur mésenchymateuse de la paupière Tumeur neurogène de la paupière Télangiectasie de la conjonctive Télangiectasie maculaire idiopathique type 3 Unclassified primitive or secondary maculopathy Usher syndrome type 2 Uvéite Uvéite antérieure infectieuse Uvéite phacoanaphylactique Vasoproliferative tumor of the retina Vernal keratoconjunctivitis Vitreoretinal degeneration Vitreoretinopathy Vitréo-rétino-choroïdopathie autosomique dominante Vitréorétinopathie inflammatoire néovasculaire autosomique dominante Vogt-Koyanagi-Harada disease WAGR syndrome Wagner disease X-linked corneal dermoid X-linked endothelial corneal dystrophy X-linked reticulate pigmentary disorder X-linked retinal dysplasia X-linked retinoschisis