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autosomal dominant nocturnal frontal lobe epilepsy 4

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNA2 gene.
Uniprot Description An autosomal dominant focal epilepsy characterized by nocturnal seizures associated with fear sensation, tongue movements, and nocturnal wandering, closely resembling nightmares and sleep walking.
Mondo Term and Equivalent IDs
MONDO:0012474:  autosomal dominant nocturnal frontal lobe epilepsy 4
MESH:C563679: 
UMLS:C1835905: