{"orpha":268829,"name":"Basal encephalocele","type":"Clinical subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-268829/","orphanet_url":"https://www.orpha.net/en/disease/detail/268829","names":{"fr":{"name":"Encéphalocèle basale"},"de":{"name":"Enzephalozele, basale"},"es":{"name":"Encefalocele basal"},"it":{"name":"Encefalocele basale"},"nl":{"name":"Basale encefalocele"},"pt":{"name":"Encefalocelo basal"},"pl":{"name":"Przepuklina mózgowa podstawna"},"cs":{"name":"Bazální encefalokéla"},"uk":{"name":"Базальне енцефалоцеле"},"zh":{"name":"基底脑膨出"},"tr":{"name":"Bazal ensefalosel"}},"xrefs":[{"source":"ICD-10","code":"Q01.8","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LA01","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"533416539"},{"source":"MONDO","code":"0017082","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C4023176","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":199647,"name":"Isolated encephalocele","classifications":[147,156,181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}