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epilepsy, familial temporal lobe, 1

Disease Summary
Associated Targets (3)
Tbio

3


Mondo Description An autosomal dominant condition caused by mutation(s) in the LGI1 gene, encoding leucine-rich glioma-inactivated protein 1. It is characterized by partial seizures originating in the temporal lobe and often accompanied by auditory sensory manifestations.
Uniprot Description A focal form of epilepsy characterized by recurrent seizures that arise from foci within the temporal lobe. Seizures are usually accompanied by sensory symptoms, most often auditory in nature.
Mondo Term and Equivalent IDs
MONDO:0700090:  epilepsy, familial temporal lobe, 1
NCIT:C141441: