SE-ATLAS

Familial pterygium of the conjunctiva Aceruloplasminemia Corneal dystrophy-perceptive deafness syndrome Blepharophimosis-ptosis-epicanthus inversus syndrome Secretory apparatus of the lacrimal system anomaly Rare disorder of the lacrimal apparatus Lacrimal drainage system anomaly Congenital alacrima Baraitser-Winter cerebrofrontofacial syndrome Epithelial recurrent erosion dystrophy Conjunctival vascular anomaly Rare disorder with conjunctival involvement as a major feature Grayson-Wilbrandt corneal dystrophy Conjunctival lymphangiectasia Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Conjunctival telangiectasia Congenital stromal corneal dystrophy Conjunctival hemangioma or hemolymphangioma Conjunctival tumor Gyrate atrophy of choroid and retina Pigmented conjunctival lesion Bulbar conjunctival dermoid or conjunctival dermolipoma Progressive retinal dystrophy due to retinol transport defect Infantile cerebellar-retinal degeneration EDICT syndrome Isolated cryptophthalmia Tarsal kink syndrome Epiblepharon Gardner syndrome Syndromic keratoconus Euryblepharon Stromal corneal dystrophy Autosomal dominant keratitis Isolated ankyloblepharon filiforme adnatum Isolated congenital ectropion Superficial corneal dystrophy Syndromic corneal dystrophy Posterior corneal dystrophy Bothnia retinal dystrophy Congenital eyelid retraction Isolated distichiasis Cone dystrophy with supernormal rod response MORM syndrome Severe early-childhood-onset retinal dystrophy X-linked corneal dermoid Corneal dystrophy Vogt-Koyanagi-Harada disease Congenital Horner syndrome Isolated congenital alacrima Keratoconus Muir-Torre syndrome Dermochondrocorneal dystrophy Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Syndromic rod-cone dystrophy Triple A syndrome Unclassified familial retinal dystrophy Genetic macular dystrophy Corneodermatoosseous syndrome Autosomal recessive bestrophinopathy Coloboma of eyelid Pigmented paravenous retinochoroidal atrophy Autosomal recessive chorioretinopathy-microcephaly syndrome Leber congenital amaurosis Intellectual disability-alacrima-achalasia syndrome AGel amyloidosis Amaurosis-hypertrichosis syndrome Helicoid peripapillary chorioretinal degeneration Lisch epithelial corneal dystrophy Meesmann corneal dystrophy Aplasia of lacrimal and salivary glands Microcephaly-lymphedema-chorioretinopathy syndrome Gelatinous drop-like corneal dystrophy Åland Islands eye disease X-linked reticulate pigmentary disorder Epithelial basement membrane dystrophy Retinal degeneration-nanophthalmos-glaucoma syndrome Subepithelial mucinous corneal dystrophy Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Late-onset retinal degeneration Reis-Bücklers corneal dystrophy Congenital fibrosis of extraocular muscles Thiel-Behnke corneal dystrophy Granular corneal dystrophy type II X-linked retinal dysplasia Granular corneal dystrophy type I Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Lattice corneal dystrophy type I Schnyder corneal dystrophy Fleck corneal dystrophy Rare palpebral disorder Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Macular corneal dystrophy Congenital hereditary endothelial dystrophy type II Rare palpebral, lacrimal system and conjunctival disease Progressive bifocal chorioretinal atrophy Revesz syndrome Central cloudy dystrophy of François Cryptophthalmia Blepharo-cheilo-odontic syndrome Congenital malformation of the eyelid Posterior amorphous corneal dystrophy Oligocone trichromacy Hereditary benign intraepithelial dyskeratosis Fuchs endothelial corneal dystrophy Pre-Descemet corneal dystrophy Eyelid border anomaly Posterior polymorphous corneal dystrophy Microblepharon-ablephara syndrome Rare eyelid malposition disorder Congenital hereditary endothelial dystrophy type I Blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome Secondary entropion Oguchi disease Congenital entropion Familial benign flecked retina Secondary ectropion Congenital ectropion Epicanthal fold Canthal anomaly Syndromic telecanthus Ablepharon macrostomia syndrome Kinetic eyelid anomaly X-linked endothelial corneal dystrophy Tumor, palpebraler Unterlidretraktion, palpebrale, kongenitale Seltene Störung mit Ptosis Beninger Tumor der palpebralen Epidermis Tumor, epidermaler palpebraler Palpebrale Epidermis, maligner Tumor der Retinitis pigmentosa Palpebrale Epidermis, präkanzeröse Läsion der Tumor, palpebraler pigmentierter Talgdrüsentumor, palpebraler Ectopia lentis-chorioretinale Dystrophie-Myopie-Syndrom Naevus, palpebraler Lentiginosis, palpebrale Blepharophimosis - epicanthus inversus - Ptosis durch Punktmutationen Tumor, palpebraler piliärer MRCS-Syndrom Tumor, palpebraler, mit vaskulärer Fehlbildung Spastische Ataxie - Hornhautdystrophie Ophthalmoplegie, chronische externe progressive, maternal-vererbte Martinique zerknitterte retinale Pigmentepitheliopathie Tumor, mesenchymatöser palpebraler Konjunktivitis, lignöse X-chromosomale Intelligenzminderung-Spastizität der Extremitäten-Netzhautdystrophie-Diabetes insipidus-Syndrom Netzhautdystrophie Augenbrauen/Augenwimpern-Anomalie, seltene Tumor, neurogener palpebraler Blepharophimosis - epicanthus inversus - Ptosis durch polyA-Expansion Pemphigoid, okuläres vernarbendes