Disease #06172 (BFIS5 (Seizures, benign familial infantile, 5), OMIM:617080)
| Official abbreviation |
BFIS5 |
| Name |
Seizures, benign familial infantile, 5 |
| OMIM ID |
617080 |
| 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 |
SCN8A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|