FAAH, fatty acid amide hydrolase, 2166

N. diseases: 177; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
0.330 GeneticVariation group BEFREE However, many works have repeatedly associated polymorphisms in the CNR1 and FAAH genes with drug-related behaviours; this suggests that these genes should be examined in further genetic studies focusing on drug addiction and other psychiatric disorders. 21937688 2012
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
0.330 Biomarker group CTD_human Divergent effects of genetic variation in endocannabinoid signaling on human threat- and reward-related brain function. 19103437 2009
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
0.330 GeneticVariation group BEFREE The relationship between the FAAH A/A genotype and risk for drug dependence in this study was drug class specific, suggesting it is not part of a more general drug abuse effect. 17290447 2007
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
0.330 GeneticVariation group BEFREE Here, we investigated the relationship of the FAAH P129T variant to a number of linked single nucleotide polymorphisms to establish a haplotyping system, calculate the estimated age and origin of the FAAH 385 C-->A mutation and evaluate its association with clinically significant drug addiction in a case control study. 16972078 2006
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
0.330 Biomarker group CTD_human A missense mutation in human fatty acid amide hydrolase associated with problem drug use. 12060782 2002