{"orpha":268950,"name":"Cerebral cortical dysplasia","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["Brain cortical dysplasia"],"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-268950/","orphanet_url":"https://www.orpha.net/en/disease/detail/268950","names":{"fr":{"name":"Dysplasie corticale cérébrale"},"de":{"name":"Dysplasie, kortikale zerebrale","synonyms":["Kortikale Dysplasie des Gehirns"]},"es":{"name":"Displasia cortical cerebral","synonyms":["Displasia cortical del cerebro"]},"it":{"name":"Displasia corticale cerebrale","synonyms":["Displasia corticale del cervello"]},"nl":{"name":"Cerebrale corticale dysplasie","synonyms":["Corticale dysplasie van de hersenen"]},"pt":{"name":"Displasia cortical cerebral","synonyms":["Displasia cortical do cérebro"]},"pl":{"name":"Dysplazja korowa mózgu","synonyms":["Brain cortical dysplasia"]},"cs":{"name":"Cerebrální kortikální dysplázie","synonyms":["Brain cortical dysplasia"]},"uk":{"name":"Дисплазія кори головного мозку","synonyms":["Дисплазія кори головного мозку"]},"zh":{"name":"大脑皮质发育不良","synonyms":["大脑皮质发育不良"]},"tr":{"name":"Serebral kortikal displazi","synonyms":["Beyin kortikal displazisi"]}},"xrefs":[{"source":"ICD-11","code":"LA05.51","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1352548261"},{"source":"MONDO","code":"0017094","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17094","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0431380","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":163209,"name":"Non-syndromic cerebral malformation due to abnormal neuronal migration","classifications":[147,156,181]}],"children":[{"orpha":729224,"name":"Epilepsy-mild cortical malformation-oligodendroglial hyperplasia","type":"Disease"},{"orpha":65683,"name":"Isolated focal cortical dysplasia","type":"Disease"}],"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}