Autosomal dominant nocturnal frontal lobe epilepsy 3

MONDO:0011545

Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNB2 gene.

Also known as: CHRNB2 autosomal dominant nocturnal frontal lobe epilepsy, ENFL3, autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNB2, autosomal dominant nocturnal frontal lobe epilepsy type 3, epilepsy, nocturnal frontal lobe, type 3, epilepsy, nocturnal frontal lobe, 3

10 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nocturnal frontal lobe epilepsy 3 itself.

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↑ Familial sleep-related hypermotor epilepsy (0)

Including sub-types (10) Tagged with Autosomal dominant nocturnal frontal lobe epilepsy 3 (0)

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