{"orpha":93968,"name":"Meningocele","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Isolated spina bifida","url":"https://raremap.alftech.space/d/ORPHA-93968/","orphanet_url":"https://www.orpha.net/en/disease/detail/93968","names":{"fr":{"name":"Méningocèle"},"de":{"name":"Meningozele"},"es":{"name":"Meningocele"},"it":{"name":"Meningocele"},"nl":{"name":"Meningocele"},"pt":{"name":"Meningocelo"},"pl":{"name":"Przepuklina oponowa"},"cs":{"name":"Meningokéla"},"uk":{"name":"Менінгоцеле"},"zh":{"name":"脑脊膜膨出"},"tr":{"name":"Meningosel"}},"xrefs":[{"source":"MeSH","code":"D008588","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"3471","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10027266","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":823,"name":"Spina bifida and other spinal dysraphisms"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}