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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 30/06/2006 |
| Symbol | FEB5 |
| Location | 6q22-q24 |
| Name | febrile convulsions, familial, 5 |
| Other name(s) |
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| Main clinical features | pure, ceased before the age of 5 years |
| Genetic determination | autosomal dominant |
| Function/system disorder | neurology |
| Type | disease |