{"orpha":155896,"name":"Otomandibular dysplasia","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-155896/","orphanet_url":"https://www.orpha.net/en/disease/detail/155896","names":{"fr":{"name":"Dysplasie oto-mandibulaire"},"de":{"name":"Dysplasie, otomandibuläre"},"es":{"name":"Displasia otomandibular"},"it":{"name":"Displasia otomandibolare"},"nl":{"name":"Otomandibulaire dysplasie"},"pt":{"name":"Displasia otomandibular"},"pl":{"name":"Dysplazja uszno-żuchwowa"},"cs":{"name":"Otomandibulární dysplázie"},"uk":{"name":"Отомандибулярна дисплазія"},"zh":{"name":"口下颌骨发育不良"},"tr":{"name":"Otomandibular displazi"}},"xrefs":[{"source":"ICD-11","code":"LD2F.16","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"424177015"},{"source":"MONDO","code":"15482","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680658","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":93453,"name":"Dysostosis with predominant craniofacial involvement","classifications":[147,156,199]},{"orpha":183583,"name":"Genetic head and neck malformation","classifications":[156]},{"orpha":68329,"name":"Rare maxillo-facial surgical disease","classifications":[209]},{"orpha":96333,"name":"Rare otorhinolaryngological malformation","classifications":[147,200]}],"children":[{"orpha":137888,"name":"Auriculocondylar syndrome","type":"Malformation syndrome"},{"orpha":141132,"name":"Craniofacial microsomia","type":"Malformation syndrome"},{"orpha":155899,"name":"Mandibulofacial dysostosis","type":"Clinical group"},{"orpha":156202,"name":"Otomandibular dysplasia associated with monogenic syndromes","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}