{"orpha":268980,"name":"Isolated focal cortical dysplasia type Ib","type":"Histopathological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":["FCD type Ib"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-268980/","orphanet_url":"https://www.orpha.net/en/disease/detail/268980","names":{"fr":{"name":"Dysplasie corticale focale isolée type Ib","synonyms":["FCD type Ib"]},"de":{"name":"Kortikale Dysplasie, fokale isolierte, Typ Ib","synonyms":["FCD Typ Ib"]},"es":{"name":"Displasia cortical focal aislada tipo Ib","synonyms":["FCD tipo Ib"]},"it":{"name":"Displasia corticale focale isolata, tipo Ib","synonyms":["FCD, tipo Ib"]},"nl":{"name":"Geïsoleerde focale corticale dysplasie type Ib","synonyms":["FCD type Ib"]},"pt":{"name":"Displasia cortical focal isolada tipo Ib","synonyms":["FCD tipo Ib"]},"pl":{"name":"Izolowana dysplazja korowa mózgu typu Ib","synonyms":["FCD typu Ib"]},"cs":{"name":"Izolovaná fokální kortikální dysplázie, typ Ib","synonyms":["FCD typ Ib"]},"uk":{"name":"Ізольована фокальна кортикальна дисплазія, тип Ib","synonyms":["FCD тип Ib"]},"zh":{"name":"孤立性局灶性脑皮质发育不良Ib型","synonyms":["FCD Ib型"]},"tr":{"name":"İzole fokal kortikal displazi tip Ib","synonyms":["FCD tip Ib"]}},"xrefs":[{"source":"ICD-10","code":"Q04.8","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LA05.51","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"409104506"},{"source":"MONDO","code":"0017097","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679765","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":268961,"name":"Isolated focal cortical dysplasia type I","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}