Disease #03637 (ETL5 (epilepsy, temporal lobe, familial, type 5 (ETL-5)), OMIM:614417)
Official abbreviation |
ETL5 |
Name |
epilepsy, temporal lobe, familial, type 5 (ETL-5) |
OMIM ID |
614417 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
CPA6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|