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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 21/06/2006 |
Symbol | FEB6 |
Location | 18p11.2 |
HGNC id | 33478 |
Name | febrile convulsions, familial, 6 |
Corresponding gene | IMPA2 |
Genetic determination | multigenic |
Function/system disorder | neurology |
Type | susceptibility factor |