FAAH2, fatty acid amide hydrolase 2, 158584

N. diseases: 11; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 GeneticVariation phenotype BEFREE We propose that genetic alterations in FAAH2 activity contribute to neurologic and psychiatric disorders in humans. 25885783 2015