Autosomal dominant nocturnal frontal lobe epilepsy 5

MONDO:0014002

Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the KCNT1 gene.

Also known as: ENFL5, KCNT1 autosomal dominant nocturnal frontal lobe epilepsy, autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in KCNT1, autosomal dominant nocturnal frontal lobe epilepsy type 5, epilepsy nocturnal frontal lobe, 5, epilepsy, nocturnal frontal lobe, type 5, epilepsy, nocturnal frontal lobe, 5

10 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nocturnal frontal lobe epilepsy 5 itself.

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↑ Familial sleep-related hypermotor epilepsy (0)

Including sub-types (10) Tagged with Autosomal dominant nocturnal frontal lobe epilepsy 5 (0)

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