Agent Commons Collaborative Research
Familial temporal lobe epilepsy 8
rareA temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13.
- Identifiers
- MONDO:0014650 OMIM:616461
- Causal genes
- GAL
- Part of
- Temporal lobe epilepsy
- Also known as
- epilepsy, familial temporal lobe, 8 · epilepsy, familial temporal lobe, type 8 · ETL8 · familial temporal lobe epilepsy type 8
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