Excel File Text File All mouse models of absence epilepsy with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      juvenile myoclonic epilepsy Efhc1tm1Kzy/Efhc1+ B6.129P2-Efhc1tm1Kzy J:145858 View
juvenile myoclonic epilepsy Efhc1tm1Kzy/Efhc1tm1Kzy B6.129P2-Efhc1tm1Kzy J:145858 View
      childhood electroclinical syndrome Cacna1atg/Cacna1atg B6.D2-Cacna1atg/J J:6154 View
juvenile myoclonic epilepsy Prkd1em1Dlp/Prkd1+ C57BL/6J-Prkd1em1Dlp J:358380 View
Lennox-Gastaut syndrome DgkdGt(RRT600)Byg/DgkdGt(RRT600)Byg involves: 129P2/OlaHsd * C57BL/6 J:126380 View
Lennox-Gastaut syndrome Gabrb3tm1.1Rmac/Gabrb3+ B6J.B6NTac(SJL)-Gabrb3tm1.1Rmac J:292112 View