{"orpha":573253,"name":"Split cord malformation type II","type":"Morphological anomaly","group":"Disorder","status":"active","flags":[],"synonyms":["Diplomyelia","SCM type 2","SCM type II","Split cord malformation type 2"],"definition":"A rare subtype of split cord malformation characterized by both hemicords included in the same single dural sac. An intradural intervening mesenchymal septum may be present.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-573253/","orphanet_url":"https://www.orpha.net/en/disease/detail/573253","names":{"fr":{"name":"Moelle épinière dédoublée type II","synonyms":["Diplomyélie","Moelle épinière dédoublée de type 2","SCM type 2","SCM type II"],"definition":"Sous-type rare de moelle épinière dédoublée caractérisé par un sac dural unique contenant les deux hémimoelles. Un septum mésenchymateux intradural peut être présent."},"de":{"name":"Split-Cord-Malformation Typ II","synonyms":["SCM Typ 2","SCM Typ II","Split-Cord-Malformation Typ 2"],"definition":"Ein seltener Subtyp des Neuralrohrdefektes, bei dem das Rückenmark in zwei Hälften gespalten ist, die beide im selben Duralsack liegen. Es kann ein intradurales intervenierendes mesenchymales Septum vorhanden sein."},"es":{"name":"Malformación de médula espinal hendida tipo II","synonyms":["Malformación de médula espinal hendida tipo 2"],"definition":"Es un subtipo poco frecuente de malformación del cordón espinal hendido caracterizada por la inclusión de ambos hemicordones en el mismo saco dural. Puede haber un tabique mesenquimatoso intradural intermedio."},"it":{"name":"Malformazione da fissurazione longitudinale del midollo spinale tipo II","synonyms":["Malformazione da fissurazione longitudinale del midollo spinale tipo 2","SCM tipo 2","SCM tipo II"]},"nl":{"name":"Gespleten ruggenmerg-malformatie type II","synonyms":["Gespleten ruggenmerg-malformatie type 2","SCM type 2","SCM type II"],"definition":"Een zeldzaam subtype van gespleten ruggenmerg-malformatie, gekenmerkt door inclusie van beide helften van het ruggenmerg in dezelfde enkele durale zak. Een intraduraal mesenchymaal septum kan aanwezig zijn."},"pt":{"name":"Malformação do cordão dividido tipo II","definition":"Subtipo raro de malformação do cordão dividido caracterizado por ambas as hemimedulas estarem incluídas no mesmo saco dural único. Pode estar presente um septo mesenquimal intradural interveniente."},"pl":{"name":"Malformacja rozszczepionego sznura typu II","synonyms":["Diplomyelia","SCM type 2","SCM type II","Split cord malformation type 2"],"definition":"Rzadki podtyp rozszczepu rdzenia kręgowego, charakteryzujący się tym, że jego obie połowy znajdują się w tym samym pojedynczym worku opony twardej. Może występować wewnątrztwardówkowa przegroda mezenchymalna."},"cs":{"name":"Diastematomyelie, typ II","synonyms":["Diplomyelia","SCM type 2","SCM type II","Split cord malformation type 2"]},"uk":{"name":"Розщеплення пуповини, тип II","synonyms":["Дипломієлія","SCM тип 2","SCM тип II","Розщеплення пуповини, тип 2"],"definition":"A rare subtype of split cord malformation characterized by both hemicords included in the same single dural sac. An intradural intervening mesenchymal septum may be present."},"zh":{"name":"脊髓分裂畸形II型","synonyms":["SCM type 2","SCM type II","Split cord malformation type 2"]},"tr":{"name":"Ayrık kordon malformasyonu tip II","synonyms":["SCM tip 2","SCM tip II","Ayrık omurilik malformasyonu tip 2"]}},"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":"MONDO","code":"0035541","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680360","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":[],"onset":["Adolescent","Adult","Childhood","Infancy"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}