Autosomal dominant nocturnal frontal lobe epilepsy 4

MONDO:0012474

Any 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

9 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by