| Metadata | |
|---|---|
| ID | DOID:0060752 |
| Name | familial temporal lobe epilepsy 5 |
| Definition | A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13. https://www.ncbi.nlm.nih.gov/pubmed/21922598 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
ETL5 [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance has material basis in some autosomal recessive inheritance |