Disease #01146 (ENFL-5 (epilepsy, frontal lobe, nocturnal, type 5 (ENFL-5)), OMIM:615005)
| Official abbreviation |
ENFL-5 |
| Name |
epilepsy, frontal lobe, nocturnal, type 5 (ENFL-5) |
| OMIM ID |
615005 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
KCNT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
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