NOS2, nitric oxide synthase 2, 4843

N. diseases: 783; N. variants: 28
Disease: Blackout - symptom ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0312422
Disease: Blackout - symptom
Blackout - symptom 		0.010 GeneticVariation phenotype BEFREE Significant associations with a number of loci were identified, including KCND2 (overly serious facial expressions), NOS2A (loss of motor skills), and NELL1 (faints, fits, or blackouts). 22935194 2013