{"orpha":156202,"name":"Otomandibular dysplasia associated with monogenic syndromes","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-156202/","orphanet_url":"https://www.orpha.net/en/disease/detail/156202","names":{"fr":{"name":"Dysplasie oto-mandibulaire des syndromes monogéniques"},"de":{"name":"Dysplasie, otomandibuläre, mit assoziierten monogenetischen Syndromen"},"es":{"name":"Displasia otomandibular asociada con síndromes monogénicos"},"it":{"name":"Displasia oto-mandibolare associata a sindromi monogeniche"},"nl":{"name":"Otomandibulaire dysplasie geassocieerd met monogene syndromen"},"pt":{"name":"Displasia otomandibular como parte de síndromes monogénicos"},"pl":{"name":"Dysplazja uszno-żuchwowa związana z zespołami monogenowymi"},"cs":{"name":"Otomandibulární dysplázie asociovaná s monogenními syndromy"},"uk":{"name":"Отомандибулярна дисплазія, повязана з моногенними синдромами"},"zh":{"name":"单基因综合征相关耳下颌骨综合征"},"tr":{"name":"Monojenik sendromları -ilişkili otomandibular displazi"}},"xrefs":[{"source":"MONDO","code":"15495","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680668","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":155896,"name":"Otomandibular dysplasia","classifications":[147,156,199,200,209]}],"children":[{"orpha":107,"name":"BOR syndrome","type":"Malformation syndrome"},{"orpha":1296,"name":"Lambert syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}