{"orpha":183512,"name":"Rare genetic 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-183512/","orphanet_url":"https://www.orpha.net/en/disease/detail/183512","names":{"fr":{"name":"Epilepsie rare de cause génétique"},"de":{"name":"Epilepsie, genetisch bedingte, seltene"},"es":{"name":"Epilepsia genética rara"},"it":{"name":"Epilessia rara genetica"},"nl":{"name":"Zeldzame genetische epilepsie"},"pt":{"name":"Epilepsia genética rara"},"pl":{"name":"Rzadka padaczka uwarunkowana genetyczniea"},"cs":{"name":"Vzácné geneticky podmíněné epilepsie"},"uk":{"name":"Рідкісна генетично обумовлена епілепсія"},"zh":{"name":"罕见遗传性癫痫"},"tr":{"name":"Nadir genetik epilepsi"}},"xrefs":[{"source":"MONDO","code":"15955","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680564","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":71859,"name":"Rare genetic neurological disorder","classifications":[156]}],"children":[{"orpha":166487,"name":"Cerebral diseases of vascular origin with epilepsy","type":"Category"},{"orpha":166478,"name":"Cerebral malformation with epilepsy","type":"Category"},{"orpha":166469,"name":"Chromosomal anomaly with epilepsy as a major feature","type":"Category"},{"orpha":166463,"name":"Epilepsy syndrome","type":"Category"},{"orpha":166475,"name":"Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes","type":"Category"},{"orpha":166481,"name":"Metabolic diseases with epilepsy","type":"Category"},{"orpha":166472,"name":"Monogenic disease with epilepsy","type":"Category"},{"orpha":166466,"name":"Neurocutaneous syndrome with epilepsy","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}