{"orpha":269190,"name":"Encephaloclastic disorder","type":"Clinical group","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-269190/","orphanet_url":"https://www.orpha.net/en/disease/detail/269190","names":{"fr":{"name":"Anomalie secondaire à une destruction cérébrale"},"de":{"name":"Enzephaloklastische Störung"},"es":{"name":"Alteraciones encefaloclásticas"},"it":{"name":"Disturbo encefaloclastico"},"nl":{"name":"Encefaloclastische stoornis"},"pt":{"name":"Doença encefaloclástica"},"pl":{"name":"Zaburzenia encefaloklastyczne"},"cs":{"name":"Encefaloklastické poruchy"},"uk":{"name":"Енцефалокластичний розлад"},"zh":{"name":"脑碎屑异常"},"tr":{"name":"Ensefaloklastik bozukluk"}},"xrefs":[{"source":"ICD-11","code":"LA05.6","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1436588898"},{"source":"MONDO","code":"0017103","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17103","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680772","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":269553,"name":"Genetic cerebral malformation","classifications":[156]},{"orpha":199633,"name":"Non-syndromic cerebral malformation","classifications":[147,181]}],"children":[{"orpha":2177,"name":"Hydranencephaly","type":"Malformation syndrome"},{"orpha":2940,"name":"Porencephaly","type":"Disease"},{"orpha":799,"name":"Schizencephaly","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}