{"orpha":268987,"name":"Isolated focal cortical dysplasia type Ic","type":"Histopathological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":["FCD type Ic"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-268987/","orphanet_url":"https://www.orpha.net/en/disease/detail/268987","names":{"fr":{"name":"Dysplasie corticale focale isolée type Ic","synonyms":["FCD type Ic"]},"de":{"name":"Kortikale Dysplasie, fokale isolierte, Typ Ic","synonyms":["FCD Typ Ic"]},"es":{"name":"Displasia cortical focal aislada tipo Ic","synonyms":["FCD tipo Ic"]},"it":{"name":"Displasia corticale focale isolata, tipo Ic","synonyms":["FCD, tipo Ic"]},"nl":{"name":"Geïsoleerde focale corticale dysplasie type Ic","synonyms":["FCD type Ic"]},"pt":{"name":"Displasia cortical focal isolada tipo Ic","synonyms":["FCD tipo Ic"]},"pl":{"name":"Izolowana dysplazja korowa mózgu typu Ic","synonyms":["FCD typu Ic"]},"cs":{"name":"Izolovaná fokální kortikální dysplázie, typ Ic","synonyms":["FCD typ Ic"]},"uk":{"name":"Ізольована фокальна кортикальна дисплазія, тип Ic","synonyms":["FCD тип Ic"]},"zh":{"name":"孤立性局灶性脑皮质发育不良Ic型","synonyms":["FCD Ic型"]},"tr":{"name":"İzole fokal kortikal displazi tip Ic","synonyms":["FCD tip Ic"]}},"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":"804344068"},{"source":"MONDO","code":"0017098","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679766","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}