{"orpha":633076,"name":"Split cord malformation, composite type","type":"Morphological anomaly","group":"Disorder","status":"active","flags":[],"synonyms":["Split cord malformation type 1.5","Split cord malformation, intermediate type","Split cord malformation, mixed type"],"definition":"A rare intermediate form of split cord malformation characterized by both hemichords encapsulated in a single dural sac with presence of an incomplete ventral or dorsal bony spur.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-633076/","orphanet_url":"https://www.orpha.net/en/disease/detail/633076","names":{"fr":{"name":"Malformation du cordon médullaire divisé, type composite","definition":"Forme intermédiaire rare de malformation du cordon médullaire divisé, caractérisée par la présence de deux hémimoelles encapsulées dans un seul sac dural, accompagnée d'un éperon osseux ventral ou dorsal incomplet."},"de":{"name":"Split-Cord-Malformation, kombinierter Typ","synonyms":["Split cord malformation, intermediärer Typ","Split-Cord-Malformation Typ 1.5","Split-Cord-Malformation, gemischter Typ"]},"es":{"name":"Malformación de médula espinal hendida, tipo compuesto","synonyms":["Malformación de médula espinal hendida, tipo 1.5","Malformación de médula espinal hendida, tipo intermedio","Malformación de médula espinal hendida, tipo mixto"]},"it":{"name":"Malformazione da fissurazione longitudinale del midollo spinale tipo composito","synonyms":["Malformazione da fissurazione longitudinale del midollo spinale tipo 1.5","Malformazione da fissurazione longitudinale del midollo spinale tipo intermedio","Malformazione da fissurazione longitudinale del midollo spinale tipo misto"]},"nl":{"name":"Gespleten ruggenmerg-malformatie, samengesteld type","synonyms":["Gespleten ruggenmerg-malformatie type 1.5","Gespleten ruggenmerg-malformatie, gemengd type","Gespleten ruggenmerg-malformatie, intermediair type"]},"pt":{"name":"Malformação de espinha bífida, tipo composto","synonyms":["Malformação de espinha bífida, tipo 1.5","Malformação de espinha bífida, tipo intermédio","Malformação de espinha bífida, tipo misto"]},"pl":{"name":"Rozszczep rdzenia, typ złożony","synonyms":["Split cord malformation type 1.5","Split cord malformation, intermediate type","Split cord malformation, mixed type"]},"cs":{"name":"Malformace s rozštěpem míchy, složený typ","synonyms":["Split cord malformation type 1.5","Split cord malformation, intermediate type","Split cord malformation, mixed type"]},"uk":{"name":"Розщеплена пуповина, комбінований тип","synonyms":["Розщеплення пуповини, тип 1.5","Розщеплення пуповини, проміжний тип","Розщеплення пуповини, змішаний тип"]}},"xrefs":[{"source":"ICD-10","code":"Q06.2","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LA07.1","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"UMLS","code":"C5816809","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":573278,"name":"Split cord malformation","classifications":[147,156,181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Unknown"],"onset":[],"prevalence":[{"type":"Cases/families","qualification":"Case(s)","class":null,"value":15.0,"area":"Worldwide","status":"Validated","source":"34802216[PMID]"},{"type":"Point prevalence","qualification":"Class only","class":"<1 / 1 000 000","value":0.0,"area":"Worldwide","status":"Validated","source":"34802216[PMID]_ORPHANET"}],"phenotypes":null}