Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2169806
Disease: recurrent muscle twitches (symptom)
recurrent muscle twitches (symptom)
0.010 GeneticVariation phenotype BEFREE Together with the common KCNE1 variant S38G, previously proposed as a genetic modifier of AF, HCN4-P883R may provide a substrate for the development of AF and TIC. 31481236 2019