{"orpha":268817,"name":"Cephalocele","type":"Clinical group","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-268817/","orphanet_url":"https://www.orpha.net/en/disease/detail/268817","names":{"fr":{"name":"Céphalocèle"},"de":{"name":"Zephalozele"},"es":{"name":"Cefalocele"},"it":{"name":"Cefalocele"},"nl":{"name":"Cefalocele"},"pt":{"name":"Cefalocelo"},"pl":{"name":"Przepuklina mózgowa"},"cs":{"name":"Cefalokéla"},"uk":{"name":"Цефалоцеле"},"zh":{"name":"脑膨出"},"tr":{"name":"Sefalosel"}},"xrefs":[{"source":"ICD-10","code":"Q01","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"LA01","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1520916568"},{"source":"MONDO","code":"0017078","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17078","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0014065","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":268843,"name":"Malformation of the neurenteric canal, spinal cord and column","classifications":[147,156,181]}],"children":[{"orpha":268820,"name":"Cranial meningocele","type":"Morphological anomaly"},{"orpha":199647,"name":"Isolated encephalocele","type":"Morphological anomaly"}],"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}