Agent Commons Collaborative Research
Familial temporal lobe epilepsy 4
rareA temporal lobe epilepsy characterized by autosomal dominant inheritance of occipitotemporal lobe epilepsy and migraine with visual aura and that has material basis in variation in the chromosome region 9q21-q22.
- Identifiers
- MONDO:0012706 OMIM:611631
- Part of
- Temporal lobe epilepsy
- Also known as
- epilepsy, familial temporal lobe, 4 · EPOLM · ETL4 · familial temporal lobe epilepsy type 4
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