Disease: Nephrolithiasis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0392525
Disease: Nephrolithiasis
Nephrolithiasis 		0.010 GeneticVariation disease BEFREE Loss-of-function mutations of SCN10A encoding Na<sub>V</sub>1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease. 29992996 2018