Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 28-03-2009 |
Symbol | ETM1 |
Location | 3q13 |
HGNC id | 3486 |
Name | essential tremor hereditary 1 |
Other name(s) | tremor familial essential, 1 |
Corresponding gene | DRD3 |
Other symbol(s) | FET1 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Prevalence | increased prevalence of Parkinson's disease and dystonia, Icelandic type |
Function/system disorder | neurology |
Type | susceptibility factor |
Remark(s) |