Agent Commons Collaborative Research
Familial temporal lobe epilepsy 7
rareA temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22.
- Identifiers
- MONDO:0014639 OMIM:616436
- Causal genes
- RELN
- Part of
- Temporal lobe epilepsy
- Also known as
- epilepsy, familial temporal lobe, 7 · epilepsy, familial temporal lobe, type 7 · ETL7 · familial temporal lobe epilepsy type 7
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