{"orpha":391479,"name":"OBSOLETE: Syndromic frontonasal dysplasia","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Syndromic median cleft syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Frontonasal dysplasia","url":"https://raremap.alftech.space/d/ORPHA-391479/","orphanet_url":"https://www.orpha.net/en/disease/detail/391479","names":{"fr":{"name":"OBSOLETE : Dysplasie fronto-nasale syndromique","synonyms":["OBSOLETE : Syndrome de la fente faciale médiane, forme syndromique"]},"de":{"name":"OBSOLET: Dysplasie, fronto-nasale, syndromale Form"},"es":{"name":"OBSOLETO: Displasia frontonasal sindrómica","synonyms":["OBSOLETO: Síndrome de fisura media facial"]},"it":{"name":"OBSOLETO: Displasia frontonasale sindromica","synonyms":["OBSOLETO: Sindrome da schisi mediana sindromica"]},"nl":{"name":"OBSOLEET: Syndromale frontonasale dysplasie","synonyms":["OBSOLEET: Syndromaal mediane splijting-syndroom"]},"pt":{"name":"OBSOLETO: Displasia frontonasal sindromática"},"pl":{"name":"NIEAKTUALNE: Syndromiczna dysplazja czolowo-nosowa","synonyms":["NIEAKTUALNE: Syndromiczny zespół rozszczepu pośrodkowego"]},"cs":{"name":"NEAKTUÁLNÍ: Syndromická frontonazální dysplázie","synonyms":["OBSOLETE: Syndromic median cleft syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Синдромальна фронтоназальна дисплазія","synonyms":["ЗАСТАРІЛО: Синдром серединної розщілини"]},"zh":{"name":"弃用：综合征性额鼻部发育不良","synonyms":["综合征性面部正中裂综合征"]},"tr":{"name":"Eski adı: Sendromik frontonazal displazi","synonyms":["Sendromik medyan yarık sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":250,"name":"Frontonasal dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}