{"orpha":166475,"name":"Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes","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-166475/","orphanet_url":"https://www.orpha.net/en/disease/detail/166475","names":{"fr":{"name":"Syndrome épileptique familial idiopathique ou cryptogénique avec gènes/loci identifiés"},"de":{"name":"Familiäres Epilepsiesyndrom, idiopathisches oder kryptogenes, mit bekanntem Gen/-ort"},"es":{"name":"Síndrome epiléptico familiar idiopático o criptogénico con genes/loci identificados"},"it":{"name":"Sindrome epilettica familiare idiopatica o criptogenetica con geni/loci identificati"},"nl":{"name":"Idiopathisch of cryptogeen familiaal epileptisch syndroom met geïdentificeerde loci/genen"},"pt":{"name":"Síndrome epiléptico familiar, idiopático ou criptogénico, com locus/gene identificado"},"pl":{"name":"Idiopatyczny lub kryptogenny rodzinny zespół padaczkowy ze zidentyfikowanym loci/genem"},"cs":{"name":"Syndromy idiopatické nebo kryptogenní dědičné epilepsie s identifikovanými lokusy/geny"},"uk":{"name":"Ідіопатичний або криптогенний синдром сімейної епілепсії з ідентифікованими локусами/генами"},"zh":{"name":"特发性或隐源性家族性癫痫综合征伴已知位点/基因"},"tr":{"name":"Tanımlanmış lokus / genler ile seyreden idiyopatik veya kriptojenik ailesel epilepsi sendromu"}},"xrefs":[{"source":"MONDO","code":"15654","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680431","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":306,"name":"Self-limited infantile epilepsy","type":"Disease"},{"orpha":140927,"name":"Self-limited neonatal/infantile epilepsy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}