{"orpha":166487,"name":"Cerebral diseases of vascular origin 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-166487/","orphanet_url":"https://www.orpha.net/en/disease/detail/166487","names":{"fr":{"name":"Maladie vasculaire cérébrale associée à une épilepsie"},"de":{"name":"Zerebrale Gefäßkrankheiten mit Epilepsie"},"es":{"name":"Enfermedades cerebrales de origen vascular con epilepsia"},"it":{"name":"Malattie cerebrali di origine vascolare con epilessia"},"nl":{"name":"Cerebrale ziektes van vasculaire oorsprong met epilepsie"},"pt":{"name":"Doença cerebral vascular com epilepsia"},"pl":{"name":"Choroba mózgu pochodzenia naczymiowego z padaczką"},"cs":{"name":"Mozkové nemoci cévního původu s epilepsií"},"uk":{"name":"Церебральні захворювання судинного походження з епілепсією"},"zh":{"name":"血管源性脑疾病伴癫痫"},"tr":{"name":"Epilepsi ile seyreden vasküler kökenli serebral hastalıklar"}},"xrefs":[{"source":"MONDO","code":"15658","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680434","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":692271,"name":"Cerebral proliferative angiopathy","type":"Disease"},{"orpha":1062,"name":"Hereditary neurocutaneous malformation","type":"Disease"},{"orpha":3205,"name":"Sturge-Weber syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}