{"orpha":268843,"name":"Malformation of the neurenteric canal, spinal cord and column","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-268843/","orphanet_url":"https://www.orpha.net/en/disease/detail/268843","names":{"fr":{"name":"Malformation du canal neurentérique et de la moelle épinière"},"de":{"name":"Fehlbildung von Canalis neurentericus, Rückenmark und Wirbelsäule"},"es":{"name":"Malformación del canal neuroentérico, la médula espinal y la columna"},"it":{"name":"Malformazione del canale neuroenterico, del midollo spinale e della colonna"},"nl":{"name":"Malformatie van neurenterisch kanaal, ruggenmerg en wervelkolom"},"pt":{"name":"Malformação do canal neuroentérico, medula espinhal e coluna"},"pl":{"name":"Malformacje kanału nerwowo-jelitowego, rdzenia kręgowego i kręgosłupa"},"cs":{"name":"Malformace neurenterického kanálu, míchy a míšního kanálu"},"uk":{"name":"Вади розвитку нервово-кишкового каналу, спинного мозку та хребта"},"zh":{"name":"神经肠管、脊髓和脊柱畸形"},"tr":{"name":"Nörenterik kanal, omurilik ve kolonun malformasyonu"}},"xrefs":[{"source":"MONDO","code":"17085","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680733","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":3388,"name":"Neural tube defect","classifications":[147,156,181]}],"children":[{"orpha":268882,"name":"Arnold-Chiari malformation type I","type":"Morphological anomaly"},{"orpha":3027,"name":"Caudal regression syndrome","type":"Malformation syndrome"},{"orpha":268817,"name":"Cephalocele","type":"Clinical group"},{"orpha":63260,"name":"Craniorachischisis","type":"Morphological anomaly"},{"orpha":63259,"name":"Iniencephaly","type":"Morphological anomaly"},{"orpha":268868,"name":"Isolated amyelia","type":"Morphological anomaly"},{"orpha":1048,"name":"Isolated anencephaly/exencephaly","type":"Morphological anomaly"},{"orpha":2789,"name":"Lateral meningocele syndrome","type":"Malformation syndrome"},{"orpha":268865,"name":"Neurenteric cyst","type":"Morphological anomaly"},{"orpha":99856,"name":"Primary syringomyelia","type":"Morphological anomaly"},{"orpha":268861,"name":"Primary tethered cord syndrome","type":"Morphological anomaly"},{"orpha":397927,"name":"Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome","type":"Malformation syndrome"},{"orpha":656126,"name":"Segmental spinal dysgenesis","type":"Disease"},{"orpha":573278,"name":"Split cord malformation","type":"Clinical group"}],"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}