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: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
0.330 GeneticVariation group BEFREE This may explain the greater vulnerability for addiction and obesity in individuals with C385A genetic variant and by extension, suggest that a D3 antagonism strategy in substance use disorders should consider FAAH C385A polymorphism. 31775159 2020
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
0.330 Biomarker group BEFREE Since then, much research interest has shifted to other cannabinoid-based strategies, such as peripheral CB1R antagonists/inverse agonists, neutral CB1R antagonists, allosteric CB1R modulators, CB2R agonists, fatty acid amide hydrolase (FAAH) inhibitors, monoacylglycerol lipase (MAGL) inhibitors, fatty acid binding protein (FABP) inhibitors, or nonaddictive phytocannabinoids with CB1R or CB2R-binding profiles, as new therapeutics for SUDs. 31549358 2019
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
0.330 Biomarker group BEFREE A single nucleotide polymorphism (SNP) in the gene encoding for fatty acid amide hydrolase (FAAH) has demonstrated association with substance use disorder diagnoses, but has not been studied with respect to these narrower phenotypes. 19002671 2009
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
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: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
0.330 Biomarker group CTD_human A missense mutation in human fatty acid amide hydrolase associated with problem drug use. 12060782 2002