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 Blepharo-cheilo-odontic syndrome Blepharophimosis-ptosis-epicanthus inversus syndrome Bothnia retinal dystrophy Central cloudy dystrophy of François Coloboma of eyelid Cone dystrophy with supernormal rod response Congenital Horner syndrome Congenital alacrima Congenital ectropion 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 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 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 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 Intellectual disability-alacrima-achalasia syndrome Isolated ankyloblepharon filiforme adnatum Isolated congenital alacrima Isolated congenital ectropion Isolated cryptophthalmia Isolated distichiasis 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 Martinique crinkled retinal pigment epitheliopathy Meesmann corneal dystrophy Microblepharon-ablephara syndrome Microcephaly-lymphedema-chorioretinopathy syndrome Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Mitochondrial DNA-related progressive external ophthalmoplegia Muir-Torre syndrome Ocular cicatricial pemphigoid Oguchi disease Oligocone trichromacy Pigmented paravenous retinochoroidal atrophy Posterior amorphous corneal dystrophy Posterior corneal dystrophy Posterior polymorphous corneal dystrophy Pre-Descemet corneal dystrophy 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 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 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 telecanthus Tarsal kink syndrome Thiel-Behnke corneal dystrophy Triple A syndrome 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 Åland Islands eye disease