| Metadata | |
|---|---|
| ID | DOID:0060748 |
| Name | familial temporal lobe epilepsy 1 |
| Definition | A temporal lobe epilepsy characterized by autosomal dominant inheritance of partial seizures originating from the temporal lobe that are often accompanied by auditory symptoms and that has_material_basis_in heterozygous mutation in the LGI1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/12205652, https://www.ncbi.nlm.nih.gov/pubmed/10851389, https://www.ncbi.nlm.nih.gov/pubmed/15079010 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
ETL1 [EXACT] partial epilepsy with auditory features [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |