Disease #04630 (BFIS2 (Seizures, benign familial infantile, type 2 (BFIS-2)), OMIM:605751)
| Official abbreviation |
BFIS2 |
| Name |
Seizures, benign familial infantile, type 2 (BFIS-2) |
| OMIM ID |
605751 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
6 |
| Associated with 1 gene |
PRRT2 |
| 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
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