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 We identified a novel missense mutation, V65 M, in the KCNE2 gene of a 17-year-old female with syncope and LQTS. 12185453 2002
CUI: C0039070
Disease: Syncope
Syncope 		0.110 Biomarker phenotype HPO