Additional Disease Briefs

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epilepsy, familial focal, with variable foci 1

Also known as: DEPDC5 epilepsy, familial focal, with variable foci, FFEVF1, epilepsy, familial focal, with variable foci, epilepsy, familial focal, with variable foci 1, epilepsy, familial focal, with variable foci caused by mutation in DEPDC5, epilepsy, partial, with variable foci


epilepsy, familial focal, with variable foci 2

Also known as: FFEVF2, NPRL2 epilepsy, familial focal, with variable foci, epilepsy, familial focal, with variable foci 2, epilepsy, familial focal, with variable foci 2; FFEVF2, epilepsy, familial focal, with variable foci caused by mutation in NPRL2, epilepsy, familial focal, with variable foci type 2


epilepsy, familial focal, with variable foci 3

Also known as: FFEVF3, NPRL3 epilepsy, familial focal, with variable foci, epilepsy, familial focal, with variable foci 3, epilepsy, familial focal, with variable foci 3; FFEVF3, epilepsy, familial focal, with variable foci caused by mutation in NPRL3, epilepsy, familial focal, with variable foci type 3



epilepsy, familial temporal lobe, 1

Also known as: ADLTE, ADPEAF, ETL1, epilepsy, familial temporal lobe, type 1, epilepsy, lateral temporal lobe, autosomal dominant, epilepsy, partial, with auditory features




epilepsy, progressive myoclonic, 1B

Also known as: EPM1B, PRICKLE1 progressive myoclonic epilepsy, epilepsy, progressive myoclonic 1B, epilepsy, progressive myoclonic, 1B, epilepsy, progressive myoclonic, type 1B, progressive myoclonic epilepsy caused by mutation in PRICKLE1