{"orpha":98565,"name":"Syndromic ankyloblepharon filiforme adnatum","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Syndromic ankyloblepharon"],"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-98565/","orphanet_url":"https://www.orpha.net/en/disease/detail/98565","names":{"fr":{"name":"Ankyloblépharon filiforme adnatum syndromique","synonyms":["Ankyloblépharon syndromique"]},"de":{"name":"Ankyloblepharon, syndromales"},"es":{"name":"Anquilobléfaron sindrómico"},"it":{"name":"Anchiloblefaron sindromico"},"nl":{"name":"Syndromaal ankyloblefaron"},"pt":{"name":"Anquiloblefaron filiforme adnatum sindromático","synonyms":["Anquiloblefaron sindromático"]},"pl":{"name":"Syndromiczne zrośnięcie brzegów powiek","synonyms":["Syndromic ankyloblepharon"]},"cs":{"name":"Syndromy se srůsty víček","synonyms":["Syndromic ankyloblepharon"]},"uk":{"name":"Синдромальний філігранний анкілоблефарон (ankyloblepharon filiforme adnatum)","synonyms":["Синдромальний анкілоблефарон"]},"zh":{"name":"综合征性丝状睑缘粘连","synonyms":["综合征性睑缘粘连"]},"tr":{"name":"Sendromik ankiloblefaron filiforme adnatum","synonyms":["Sendromik ankiloblefaron"]}},"xrefs":[{"source":"UMLS","code":"C5680329","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98564,"name":"Eyelid border anomaly","classifications":[147,156,189]}],"children":[{"orpha":1071,"name":"Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","type":"Malformation syndrome"},{"orpha":1791,"name":"Frontofacionasal dysplasia","type":"Malformation syndrome"},{"orpha":85275,"name":"Microphthalmia-ankyloblepharon-intellectual disability syndrome","type":"Malformation syndrome"},{"orpha":294963,"name":"Popliteal pterygium syndrome","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}