{"orpha":156215,"name":"Oromandibular-limb anomalies syndrome","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-156215/","orphanet_url":"https://www.orpha.net/en/disease/detail/156215","names":{"fr":{"name":"Syndrome oro-mandibulaire-anomalies des membres"},"de":{"name":"Oromandibuläre Fehlbildung und Extremitätenanomalien"},"es":{"name":"Síndrome de anomalía oromandibular y de las extremidades"},"it":{"name":"Sindrome da anomalie oromandibolari e degli arti"},"nl":{"name":"Oromandibulaire-ledemaatanomalieënsyndroom"},"pt":{"name":"Síndrome oromandibular-anomalias dos membros"},"pl":{"name":"Zespół wad ustno-żuchwowo-kończynowych"},"cs":{"name":"Oromandibulární syndrom s anomáliemi končetin"},"uk":{"name":"Синдром рото-нижньощелепних аномалій та аномалій кінцівок"},"zh":{"name":"口下颌-肢体畸形综合征"},"tr":{"name":"Oromandibuler-ekstremite anomalileri sendromu"}},"xrefs":[{"source":"ICD-11","code":"LD25.0","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1868700139"},{"source":"MONDO","code":"0015498","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15498","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680663","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":156212,"name":"Hypoglossia/aglossia","classifications":[147,156,209]}],"children":[{"orpha":140997,"name":"Orofaciodigital syndrome","type":"Clinical group"},{"orpha":2749,"name":"Oromandibular-limb hypogenesis syndrome","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}