ALAD, aminolevulinate dehydratase, 210

N. diseases: 135; N. variants: 8
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 		0.010 GeneticVariation disease BEFREE These results suggest that the ALAD rs1800435 SNP is not related with the risk for ET, but its interaction with the HMOX2 rs1051308 SNP could be weakly associated with the risk for this disease. 28276576 2017