FAAH, fatty acid amide hydrolase, 2166

N. diseases: 177; N. variants: 8
Disease: Substance Dependence ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038580
Disease: Substance Dependence
Substance Dependence 		0.310 Biomarker disease CTD_human Divergent effects of genetic variation in endocannabinoid signaling on human threat- and reward-related brain function. 19103437 2009
CUI: C0038580
Disease: Substance Dependence
Substance Dependence 		0.310 Biomarker disease CTD_human A missense mutation in human fatty acid amide hydrolase associated with problem drug use. 12060782 2002
CUI: C0038580
Disease: Substance Dependence
Substance Dependence 		0.310 GeneticVariation disease BEFREE Although a link between the FAAH P129T variant and human drug abuse has been reported, the extent of risk and specific types of substance addiction vulnerability remain to be determined. 16972078 2006