HMOX2, heme oxygenase 2, 3163

N. diseases: 31; N. variants: 4
Disease: Essential Tremor ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.020 GeneticVariation disease BEFREE Subjects carrying the ALAD rs1800435CC genotype (wild-type) and the HMOX2 rs1051308GG genotype or the HMOX2 rs1051308G allele had significantly decreased risk for ET. 28276576 2017
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.020 GeneticVariation disease BEFREE The present study suggests a weak association between HMOX1 rs2071746 and HMOX2 rs1051308 polymorphisms and the risk to develop ET in the Spanish population. 26091465 2015