Disease #04645 (ETL7 (epilepsy, temporal lobe, familial, type 7 (ETL-7)), OMIM:616436)
| Official abbreviation |
ETL7 |
| Name |
epilepsy, temporal lobe, familial, type 7 (ETL-7) |
| OMIM ID |
616436 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
RELN |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|