ETM2, essential tremor 2, 2112

N. diseases: 3; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.060 Biomarker disease BEFREE To date, linkage analyses revealed three loci associated to essential tremor (ET) (ETM1 on 3q13, ETM2 on 2p22-25, and a locus on 6p23). 17703985 2008
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.060 GeneticVariation disease BEFREE Our data thus support that ET development would be linked with the ETM2 locus and will facilitate the search for the ETM2 gene transcript. 16092108 2005
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.060 GeneticVariation disease BEFREE Linkage disequilibrium studies in separate population samples from the United States and Singapore suggest an association between ET and loci at ETM2. 15699368 2005
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.060 Biomarker disease LHGDN Integrated physical map of the human essential tremor gene region (ETM2) on chromosome 2p24.3-p24.2. 15108195 2004
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.060 GeneticVariation disease BEFREE A gene for autosomal dominant familial essential tremor maps to a 9.1 cM interval flanked by loci D2S224 and D2S405 (ETM2) on human chromosome 2p24.3-p24.2. 15108195 2004
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.060 GeneticVariation disease BEFREE Six polymorphic loci (etm1240, etm1231, etm1234, APOB, etm1241, and etm1242) in a 274-kb interval within an ET gene candidate region (ETM2) were analyzed in Singaporean individuals with a family history of ET (n = 52) and compared to Singaporean controls older than age 65 (n = 49). 15355439 2004
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.060 GeneticVariation disease BEFREE Haplotype analysis of the ETM2 locus in familial essential tremor. 12761658 2003
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation disease BEFREE Haplotype analysis at the ETM2 locus in a Singaporean sample with familial essential tremor. 15355439 2004
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.010 Biomarker group BEFREE ET is a common movement disorder that is genetically linked to ETM2 in four large families. 12761658 2003