{"orpha":166466,"name":"Neurocutaneous syndrome with epilepsy","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-166466/","orphanet_url":"https://www.orpha.net/en/disease/detail/166466","names":{"fr":{"name":"Syndrome neurocutané associé à une épilepsie"},"de":{"name":"Neurokutanes Syndrom mit Epilepsie"},"es":{"name":"Síndrome neurocutáneo con epilepsia"},"it":{"name":"Sindrome neurocutanea associata ad epilessia"},"nl":{"name":"Neurocutaan syndroom met epilepsie"},"pt":{"name":"Síndrome neurocutâneo com epilepsia"},"pl":{"name":"Zespół nerwowo-skórny z padaczką"},"cs":{"name":"Neurokutánní syndromy s epilepsií"},"uk":{"name":"Нейрошкірний синдром з епілепсією"},"zh":{"name":"神经皮肤综合征伴癫痫"},"tr":{"name":"Epilepsi ile seyreden nörokutanöz sendrom"}},"xrefs":[{"source":"MONDO","code":"15651","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680427","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":101998,"name":"Rare epilepsy","classifications":[181]},{"orpha":183512,"name":"Rare genetic epilepsy","classifications":[156]}],"children":[{"orpha":100,"name":"Ataxia-telangiectasia","type":"Disease"},{"orpha":464,"name":"Incontinentia pigmenti","type":"Malformation syndrome"},{"orpha":33445,"name":"Neuroectodermal melanolysosomal disease","type":"Malformation syndrome"},{"orpha":636,"name":"Neurofibromatosis type 1","type":"Disease"},{"orpha":744,"name":"Proteus syndrome","type":"Malformation syndrome"},{"orpha":3205,"name":"Sturge-Weber syndrome","type":"Malformation syndrome"},{"orpha":805,"name":"Tuberous sclerosis complex","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}