{"orpha":563951,"name":"Isolated congenital aglossia","type":"Clinical subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This disease is described under Isolated congenital hypoglossia/aglossia","url":"https://raremap.alftech.space/d/ORPHA-563951/","orphanet_url":"https://www.orpha.net/en/disease/detail/563951","names":{"fr":{"name":"Aglossie isolée congénitale"},"de":{"name":"Aglossie, isolierte, kongenitale"},"es":{"name":"Aglosia congénita aislada"},"it":{"name":"Aglossia congenita isolata"},"nl":{"name":"Geïsoleerde congenitale aglossie"},"pt":{"name":"Aglossia congénita isolada"},"pl":{"name":"Izolowany wrodzony brak języka"},"cs":{"name":"Izolovaná vrozená aglosie"},"uk":{"name":"Ізольована вроджена аглосія"},"zh":{"name":"孤立性先天性无舌"},"tr":{"name":"İzole doğumsal aglossi"}},"xrefs":[{"source":"ICD-10","code":"Q38.3","qualifier":"NTBT","icd_relation":"inclusion","validated":true},{"source":"ICD-11","code":"LA31.1","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"996394083"},{"source":"MONDO","code":"0035410","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0158663","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10001501","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":141152,"name":"Isolated congenital hypoglossia/aglossia","classifications":[147,156,209]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}