{"context":{"query":"EPILEPSY"},"stats":{"total":50},"pagination":{"has_next":true,"next_token":"0,0,-1,50"},"schema":"id|dataset|name|xref_count","data":["C537297|mesh|Autosomal Dominant Lateral Temporal Lobe Epilepsy|2","C536956|mesh|Temporal epilepsy, familial|2","C535285|mesh|Ramon Syndrome|2","C535496|mesh|Epilepsy occipital calcifications|1","C563719|mesh|Generalized Epilepsy and Paroxysmal Dyskinesia|152","C563695|mesh|Photoparoxysmal Response 3|1","C535497|mesh|Epilepsy telangiectasia|2","C563679|mesh|Epilepsy, Nocturnal Frontal Lobe, Type 4|101","C563550|mesh|Myoclonic Epilepsy, Hartung Type|1","C537052|mesh|Alopecia epilepsy oligophrenia syndrome of Moynahan|2","C563425|mesh|Diabetes Mellitus, Permanent Neonatal|207","C563399|mesh|Epilepsy, Myoclonic, Benign Adult Familial, Type 1|55","C562694|mesh|Epilepsy, Idiopathic Generalized|282","C535499|mesh|Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp|75","C562568|mesh|Cerebellar Hypoplasia|2","C557674|mesh|SeSAME syndrome|73","C548070|mesh|Pontocerebellar Hypoplasia Type 2|2","C537213|mesh|Kohlschutter Tonz syndrome|81","C537625|mesh|Gurrieri Sammito Bellussi syndrome|2","C537563|mesh|Jankovic Rivera syndrome|2","C536254|mesh|Pyridoxine-dependent epilepsy|223","C536575|mesh|Borjeson-Forssman-Lehmann syndrome|83","C538091|mesh|Kuzniecky syndrome|2","C537057|mesh|Alopecia, epilepsy, pyorrhea, mental subnormality|2","C536869|mesh|Spastic paraplegia epilepsy mental retardation|1","C537066|mesh|Flynn Aird syndrome|2","EFO:0009647|efo|epilepsy, hearing loss, and intellectual disability syndrome|1413","EFO:1001090|efo|partial sensory epilepsy|1357","EFO:1001900|efo|myoclonic epilepsy|1432","EFO:0000773|efo|temporal lobe epilepsy|1424","EFO:0000474|efo|epilepsy|1829","EFO:0007262|efo|epilepsy with generalized tonic-clonic seizures|1501","EFO:1001146|efo|reflex epilepsy|1357","EFO:0005917|efo|generalised epilepsy|1442","EFO:0004263|efo|partial epilepsy|1542","EFO:1001010|efo|Landau-Kleffner syndrome|2561","EFO:1001093|efo|Pelger-Huet anomaly|1342","EFO:1001089|efo|partial motor epilepsy|1385","EFO:1000877|efo|complex partial epilepsy|1398","EFO:0010739|efo|epilepsy, early-onset, with or without developmental delay|1354","EFO:0700024|efo|familial mesial temporal lobe epilepsy with febrile seizures|1487","EFO:0700037|efo|benign familial mesial temporal lobe epilepsy|1353","EFO:0700105|efo|myoclonic epilepsy of infancy|1363","MONDO:0003290|mondo|simple partial epilepsy|38","MONDO:0007085|mondo|alopecia-epilepsy-pyorrhea-intellectual disability syndrome|166","MONDO:0009077|mondo|deafness, congenital, and familial myoclonic epilepsy|4","MONDO:0008755|mondo|Moynahan syndrome|162","MONDO:0005027|mondo|epilepsy|987","MONDO:0008939|mondo|isolated cerebellar hypoplasia/agenesis|186","MONDO:0005115|mondo|temporal lobe epilepsy|75"]}