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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 19-06-2018 |
Symbol | BFIS2 |
Location | 16p11.2 |
Name | seizures, benign familial infantile, 2 |
Corresponding gene | PRRT2 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | neurology |
Type | disease |
Remark(s) |