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autosomal dominant nocturnal frontal lobe epilepsy 1

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNA4 gene.
Uniprot Description An autosomal dominant focal epilepsy characterized by nocturnal seizures with hyperkinetic automatisms and poorly organized stereotyped movements.
Mondo Term and Equivalent IDs
MONDO:0010899:  autosomal dominant nocturnal frontal lobe epilepsy 1
MESH:C563930: 
UMLS:C1838049: