essential tremor Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A movement disorder that causes involuntary tremors, especially in the hands. It occurs alone without other neurological signs and symptoms. (Human Disease Ontology, DOID_4990)
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13 genes associated with the disease essential tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADH1B alcohol dehydrogenase 1B (class I), beta polypeptide
ALAD aminolevulinate dehydratase
APOB apolipoprotein B
CYP2C8 cytochrome P450, family 2, subfamily C, polypeptide 8
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
DRD3 dopamine receptor D3
ETM2 essential tremor 2
FMR1 fragile X mental retardation 1
GSTP1 glutathione S-transferase pi 1
LINGO1 leucine rich repeat and Ig domain containing 1
LRRK2 leucine-rich repeat kinase 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
SCN8A sodium channel, voltage gated, type VIII alpha subunit