SE-ATLAS

AGel amyloidosis Ablepharon macrostomia syndrome Aceruloplasminemia Amaurosis-hypertrichosis syndrome Aplasia of lacrimal and salivary glands Autosomal dominant keratitis Autosomal recessive bestrophinopathy Autosomal recessive chorioretinopathy-microcephaly syndrome Baraitser-Winter cerebrofrontofacial syndrome Benign tumor of palpebral epidermis Blepharo-cheilo-odontic syndrome Blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome Blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome Blepharophimosis-epicanthus inversus-ptosis due to copy number variations Blepharophimosis-ptosis-epicanthus inversus syndrome Bothnia retinal dystrophy Bulbar conjunctival dermoid or conjunctival dermolipoma Canthal anomaly Central cloudy dystrophy of François Coloboma of eyelid Cone dystrophy with supernormal rod response Congenital Horner syndrome Congenital alacrima Congenital ectropion Congenital entropion Congenital eyelid retraction Congenital fibrosis of extraocular muscles Congenital hereditary endothelial dystrophy type I Congenital hereditary endothelial dystrophy type II Congenital malformation of the eyelid Congenital stromal corneal dystrophy Congenital upper palpebral retraction Conjunctival hemangioma or hemolymphangioma Conjunctival lymphangiectasia Conjunctival telangiectasia Conjunctival tumor Conjunctival vascular anomaly Corneal dystrophy Corneal dystrophy-perceptive deafness syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Corneodermatoosseous syndrome Cryptophthalmia Dermochondrocorneal dystrophy EDICT syndrome Ectopia lentis-chorioretinal dystrophy-myopia syndrome Epiblepharon Epicanthal fold Epithelial basement membrane dystrophy Epithelial recurrent erosion dystrophy Euryblepharon Eyelid border anomaly Familial benign flecked retina Familial pterygium of the conjunctiva Fleck corneal dystrophy Fuchs endothelial corneal dystrophy Gardner syndrome Gelatinous drop-like corneal dystrophy Genetic macular dystrophy Granular corneal dystrophy type I Granular corneal dystrophy type II Grayson-Wilbrandt corneal dystrophy Gyrate atrophy of choroid and retina Helicoid peripapillary chorioretinal degeneration Hereditary benign intraepithelial dyskeratosis Infantile cerebellar-retinal degeneration Inherited retinal disorder Intellectual disability-alacrima-achalasia syndrome Isolated ankyloblepharon filiforme adnatum Isolated congenital alacrima Isolated congenital ectropion Isolated cryptophthalmia Isolated distichiasis Keratoconus Kinetic eyelid anomaly Lacrimal drainage system anomaly Late-onset retinal degeneration Lattice corneal dystrophy type I Leber congenital amaurosis Ligneous conjunctivitis Lisch epithelial corneal dystrophy MORM syndrome MRCS syndrome Macular corneal dystrophy Malignant tumor of palpebral epidermis Martinique crinkled retinal pigment epitheliopathy Meesmann corneal dystrophy Mesenchymatous palpebral tumor Microblepharon-ablephara syndrome Microcephaly-lymphedema-chorioretinopathy syndrome Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Mitochondrial DNA-related progressive external ophthalmoplegia Muir-Torre syndrome Neurogenic palpebral tumor Ocular cicatricial pemphigoid Oguchi disease Oligocone trichromacy Palpebral epidermal tumor Palpebral lentiginosis Palpebral nevus Palpebral piliary tumor Palpebral sebaceous gland tumor Palpebral tumor Palpebral tumor with a vascular malformation Pigmented conjunctival lesion Pigmented palpebral tumor Pigmented paravenous retinochoroidal atrophy Posterior amorphous corneal dystrophy Posterior corneal dystrophy Posterior polymorphous corneal dystrophy Pre-Descemet corneal dystrophy Precancerous lesion of palpebral epidermis Progressive bifocal chorioretinal atrophy Progressive retinal dystrophy due to retinol transport defect Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Rare disorder of the lacrimal apparatus Rare disorder with conjunctival involvement as a major feature Rare disorder with ptosis Rare eyebrow/eyelash disorder Rare eyelid malposition disorder Rare palpebral disorder Rare palpebral, lacrimal system and conjunctival disease Reis-Bücklers corneal dystrophy Retinal degeneration-nanophthalmos-glaucoma syndrome Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Retinitis pigmentosa Revesz syndrome Schnyder corneal dystrophy Secondary ectropion Secondary entropion Secretory apparatus of the lacrimal system anomaly Severe early-childhood-onset retinal dystrophy Spastic ataxia-corneal dystrophy syndrome Stromal corneal dystrophy Subepithelial mucinous corneal dystrophy Superficial corneal dystrophy Syndromic corneal dystrophy Syndromic keratoconus Syndromic rod-cone dystrophy Syndromic telecanthus Tarsal kink syndrome Thiel-Behnke corneal dystrophy Triple A syndrome Unclassified familial retinal dystrophy Vogt-Koyanagi-Harada disease X-linked corneal dermoid X-linked endothelial corneal dystrophy X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome X-linked reticulate pigmentary disorder X-linked retinal dysplasia Åland Islands eye disease