{"orpha":98948,"name":"Congenital symblepharon","type":"Clinical subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This disease is described under Isolated cryptophthalmia","url":"https://raremap.alftech.space/d/ORPHA-98948/","orphanet_url":"https://www.orpha.net/en/disease/detail/98948","names":{"fr":{"name":"Symblépharon congénital"},"de":{"name":"Symblepharon, kongenitales"},"es":{"name":"Simbléfaron congénito"},"it":{"name":"Simblefaron congenito"},"nl":{"name":"Congenitale symblefaron"},"pt":{"name":"Simblefaron congénito"},"pl":{"name":"Wrodzone zrośnięcie powieki z gałką oczną"},"cs":{"name":"Vrozený symblefaron"},"uk":{"name":"Вроджений симблефарон"},"zh":{"name":"先天性睑球粘连"},"tr":{"name":"Doğumsal sembleferon"}},"xrefs":[{"source":"ICD-10","code":"Q11.2","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LA14.01","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1595154985"},{"source":"MONDO","code":"0020359","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0152454","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":91396,"name":"Isolated cryptophthalmia","classifications":[147,156,189]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["Antenatal","Neonatal"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"<1 / 1 000 000","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET_3099574[PMID]"}],"phenotypes":null}