{"orpha":98631,"name":"Congenital malformation of the eye with glaucoma as a major feature","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-98631/","orphanet_url":"https://www.orpha.net/en/disease/detail/98631","names":{"fr":{"name":"Malformation congénitale de l'oeil avec glaucome comme manifestation majeure"},"de":{"name":"Glaucoma, secondary dysgenetic"},"es":{"name":"Glaucoma disgenético secundario"},"it":{"name":"Glaucoma secondario disgenetico"},"nl":{"name":"Congenitale malformatie van oog met glaucoom als hoofdkenmerk"},"pt":{"name":"Malformação do olho com glaucoma como característica principal"},"pl":{"name":"Wtórna jaskra dysgenetyczna"},"cs":{"name":"Sekundární glaukom u dysgeneze předního segmentu"},"uk":{"name":"Вроджена вада розвитку ока з глаукомою як основною ознакою"},"zh":{"name":"以青光眼为特征先天性眼畸形"},"tr":{"name":"Esas klinik özelliği glokomlu göz olan doğumsal malformasyon"}},"xrefs":[{"source":"UMLS","code":"C5681671","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98553,"name":"Developmental defect of the eye","classifications":[147]},{"orpha":519331,"name":"Secondary early-onset glaucoma","classifications":[189]}],"children":[{"orpha":98634,"name":"Anterior segment developmental anomaly without extraocular manifestations","type":"Category"},{"orpha":190,"name":"Coats disease","type":"Disease"},{"orpha":238763,"name":"Glaucoma secondary to spherophakia/ectopia lentis and megalocornea","type":"Malformation syndrome"},{"orpha":64734,"name":"Iridocorneal endothelial syndrome","type":"Disease"},{"orpha":35612,"name":"Isolated complete colobomatous microphthalmia","type":"Clinical subtype"},{"orpha":94058,"name":"Neovascular glaucoma","type":"Particular clinical situation in a disease or syndrome"},{"orpha":98973,"name":"Posterior polymorphous corneal dystrophy","type":"Disease"},{"orpha":792,"name":"X-linked retinoschisis","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}