Disease: Syncope ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039070
Disease: Syncope
Syncope 		0.110 GeneticVariation phenotype BEFREE Besides identifying 8 SCN5A mutations in the present cohort, a KCNE3 T4A mutation was found in a 55-year-old male patient who had experienced several episodes of syncope. 22987075 2012
CUI: C0039070
Disease: Syncope
Syncope 		0.110 Biomarker phenotype HPO