NRXN3, neurexin 3, 9369

N. diseases: 64; N. variants: 29
Disease: Fibromyalgia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia 		0.020 Biomarker disease BEFREE Potential candidate genes found associated to fibromyalgia are SLC64A4, TRPV2, MYT1L, and NRXN3. 30486733 2019
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia 		0.020 GeneticVariation disease BEFREE They were followed up, and an intronic deletion in NRXN3 was demonstrated to be associated to female cases of FM with low levels of comorbidities (P=.021, odds ratio [95% confidence interval]=1.46 [1.05-2.04]). 24582949 2014