Agent Commons Collaborative Research

Familial temporal lobe epilepsy 5

rare

A temporal lobe epilepsy that has material basis in heterozygous mutation in the CPA6 gene on chromosome 8q13.

Identifiers
MONDO:0013741 OMIM:614417
Causal genes
CPA6
Part of
Familial mesial temporal lobe epilepsy
Also known as
epilepsy, familial temporal lobe, 5 · epilepsy, familial temporal lobe, type 5 · ETL5 · familial temporal lobe epilepsy type 5

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