SE-ATLAS

Keratoconus Treacher-Collins syndrome Intermediate uveitis Congenital myasthenic syndrome Centronuclear myopathy X-linked centronuclear myopathy Posterior uveitis Anterior uveitis Proximal myotonic myopathy Cornelia de Lange syndrome Panuveitis Essential strabismus Goldberg-Shprintzen megacolon syndrome Syndromic disorder with strabismus Congenital fibrosis of extraocular muscles Tremor-nystagmus-duodenal ulcer syndrome Aniridia Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome Syndromic aniridia Neovascular glaucoma Pediatric-onset glaucoma of genetic origin Congenital glaucoma Dopamine beta-hydroxylase deficiency Secondary entropion Juvenile glaucoma Congenital entropion Secondary ectropion Congenital ectropion Dubowitz syndrome Isolated aniridia Uveitis Rare disorder with ptosis Noonan syndrome Oculogastrointestinal muscular dystrophy X-linked myotubular myopathy-abnormal genitalia syndrome Primary early-onset glaucoma Early-onset non-syndromic cataract Saethre-Chotzen syndrome Acrootoocular syndrome Mitochondrial DNA-related progressive external ophthalmoplegia Char syndrome Atrioventricular defect-blepharophimosis-radial and anal defect syndrome Jacobsen syndrome Blepharophimosis-ptosis-epicanthus inversus syndrome Congenital primary aphakia Borjeson-Forssman-Lehmann syndrome Baraitser-Winter cerebrofrontofacial syndrome Ptosis-vocal cord paralysis syndrome Oculopharyngeal muscular dystrophy Ptosis-strabismus-ectopic pupils syndrome Smith-Lemli-Opitz syndrome Steinert myotonic dystrophy Syndromic keratoconus Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome Oculopharyngodistal myopathy Congenital malformation of the eye with glaucoma as a major feature Cataract-glaucoma syndrome Mitochondrial neurogastrointestinal encephalomyopathy Congenital ptosis Rare disorder with lens opacification Blepharophimosis-radioulnar synostosis syndrome Congenital Horner syndrome Syndromic cataract Marcus-Gunn syndrome Mucopolysaccharidosis type 2