{"orpha":141253,"name":"Oblique facial cleft","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["Orbitofacial cleft"],"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-141253/","orphanet_url":"https://www.orpha.net/en/disease/detail/141253","names":{"fr":{"name":"Fente faciale oblique","synonyms":["Fente orbito-faciale"]},"de":{"name":"Gesichtsspalte, schräge"},"es":{"name":"Hendidura facial oblicua","synonyms":["Hendidura orbitofacial"]},"it":{"name":"Schisi facciale obliqua"},"nl":{"name":"Schuine aangezichtsspleet","synonyms":["Orbitofaciale spijting"]},"pt":{"name":"Fenda oblíqua facial"},"pl":{"name":"Skośny rozszczep twarzy","synonyms":["Rozszczep oczodołowo-twarzowy"]},"cs":{"name":"Šikmý rozštěp obličeje","synonyms":["Orbitofaciální rozštěp"]},"uk":{"name":"Коса розщілина обличчя","synonyms":["Орбіто-лицьова розщілина"]},"zh":{"name":"斜面裂","synonyms":["眶面裂"]},"tr":{"name":"Eğik yüz yarığı","synonyms":["Orbitofasiyal yarık"]}},"xrefs":[{"source":"MONDO","code":"15415","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679604","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":141229,"name":"Facial cleft","classifications":[147,209]}],"children":[{"orpha":155889,"name":"Coloboma of inferior eyelid","type":"Morphological anomaly"},{"orpha":155884,"name":"Coloboma of superior eyelid","type":"Morphological anomaly"},{"orpha":141258,"name":"Tessier number 4 facial cleft","type":"Morphological anomaly"},{"orpha":141261,"name":"Tessier number 5 facial cleft","type":"Morphological anomaly"},{"orpha":141265,"name":"Tessier number 6 facial cleft","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["Infancy","Neonatal"],"prevalence":[{"type":"Prevalence at birth","qualification":"Value and class","class":"1-9 / 1 000 000","value":0.31,"area":"United States","status":"Not yet validated","source":"21703590[PMID]_ORPHANET"},{"type":"Point prevalence","qualification":"Class only","class":"1-9 / 1 000 000","value":0.0,"area":"United States","status":"Not yet validated","source":"21703590[PMID]_ORPHANET"},{"type":"Point prevalence","qualification":"Class only","class":"1-9 / 1 000 000","value":0.0,"area":"Europe","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}