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 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
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