Additional Disease Briefs
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
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
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
Also known as:
FFEVF4, epilepsy, FAMILIAL focal, with variable foci 4
Also known as:
ADLTE, ADPEAF, ETL1, epilepsy, familial temporal lobe, type 1, epilepsy, lateral temporal lobe, autosomal dominant, epilepsy, partial, with auditory features
Also known as:
EPILEPSY, PROGRESSIVE MYOCLONIC, 11, EPM11, epilepsy, progressive myoclonic, 11
Also known as:
EPM12, epilepsy, progressive myoclonic, 12
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
Also known as:
IECEE1, developmental and epileptic encephalopathy 91, epileptic encephalopathy, infantile or early childhood, 1
Also known as:
IECEE2, developmental and epileptic encephalopathy 92, epileptic encephalopathy, infantile or early childhood, 2