Autosomal dominant nocturnal frontal lobe epilepsy 4
MONDO:0012474Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNA2 gene.
Also known as: CHRNA2 autosomal dominant nocturnal frontal lobe epilepsy, ENFL4, autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA2, autosomal dominant nocturnal frontal lobe epilepsy type 4, epilepsy, nocturnal frontal lobe, type 4, convulsions, benign familial infantile, 6, epilepsy, familial, with nocturnal wandering and Ictal fear, epilepsy, nocturnal frontal lobe, 4
10 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nocturnal frontal lobe epilepsy 4 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.