{"orpha":163209,"name":"Non-syndromic cerebral malformation due to abnormal neuronal migration","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Brain malformation due to abnormal neuronal migration"],"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-163209/","orphanet_url":"https://www.orpha.net/en/disease/detail/163209","names":{"fr":{"name":"Malformation cérébrale non syndromique due à une anomalie de la migration neuronale"},"de":{"name":"Zerebrale Fehlbildung durch neuronalen Migrationsdefekt, nichtsyndromal","synonyms":["Hirnfehlbildung durch Anomalie der neuronalen Migration"]},"es":{"name":"Malformación cerebral no sindrómica por migración neuronal anómala","synonyms":["Malformación del cerebro por migración neuronal anómala"]},"it":{"name":"Malformazione cerebrale non sindromica da difetto della migrazione neuronale","synonyms":["Malformazione cerebrale da difetto della migrazione neuronale"]},"nl":{"name":"Niet-syndromale cerebrale malformatie door abnormale neuronale migratie","synonyms":["Hersenmalformatie door abnormale neuronale migratie"]},"pt":{"name":"Doença neurológica por migração neuronal anómala"},"pl":{"name":"Niesyndromiczna malformacja mózgu z powodu nieprawidłowej migracji neuronów","synonyms":["Malformacja mózgu z powodu nieprawidłowej migracji neuronów"]},"cs":{"name":"Nesyndromické malformace mozku způsobené abnormální neuronální migrací","synonyms":["Malformace mozku způsobené abnormální neuronální migrací"]},"uk":{"name":"Несиндромальна церебральна мальформація внаслідок аномальної міграції нейронів","synonyms":["Вади розвитку мозку через аномальну міграцію нейронів"]},"zh":{"name":"神经元异常迁移所致非综合征性脑畸形","synonyms":["神经元异常迁移所致脑畸形"]},"tr":{"name":"Anormal nöronal migrasyon nedeniyle sendromik olmayan serebral malformasyon","synonyms":["Anormal nöronal göçe bağlı beyin malformasyonu"]}},"xrefs":[{"source":"MONDO","code":"15572","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679571","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":1139,"name":"OBSOLETE: Arthrogryposis-epileptic seizures-migrational brain disorder syndrome","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":166478,"name":"Cerebral malformation with epilepsy","classifications":[156,181]},{"orpha":269553,"name":"Genetic cerebral malformation","classifications":[156]},{"orpha":199633,"name":"Non-syndromic cerebral malformation","classifications":[147,181]}],"children":[{"orpha":329329,"name":"Autosomal recessive frontotemporal pachygyria","type":"Malformation syndrome"},{"orpha":268950,"name":"Cerebral cortical dysplasia","type":"Clinical group"},{"orpha":300570,"name":"Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation","type":"Disease"},{"orpha":2149,"name":"Nodular neuronal heterotopia","type":"Morphological anomaly"},{"orpha":280640,"name":"Occipital pachygyria and polymicrogyria","type":"Malformation syndrome"},{"orpha":2798,"name":"Pachygyria-intellectual disability-epilepsy syndrome","type":"Malformation syndrome"},{"orpha":35981,"name":"Polymicrogyria","type":"Clinical group"},{"orpha":99796,"name":"Subcortical band heterotopia","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}