# familial temporal lobe epilepsy 7

> 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

**Wikidata**: [Q3589154](https://www.wikidata.org/wiki/Q3589154)  
**Source**: https://4ort.xyz/entity/familial-temporal-lobe-epilepsy-7


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)