Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0853946
Disease: Pain worsened
Pain worsened
0.010 GeneticVariation phenotype BEFREE Human loss or gain-of-function mutations in the gene encoding Na<sub>v</sub>1.7 channels (SCN9A) are associated with either absence of pain, as reported for congenital insensitivity to pain, or with exacerbation of pain, as reported for primary erythromelalgia and paroxysmal extreme pain disorder. 29166836 2018