Disease: Syncope ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039070
Disease: Syncope
Syncope 		0.410 GeneticVariation phenotype BEFREE We studied a five-generation family, in which a CACNA1C variant c.2573G>A p.Arg858His co-segregates with syncope and cardiac arrest, documenting electrocardiographic data and cardiac symptomatology. 30345660 2019
CUI: C0039070
Disease: Syncope
Syncope 		0.410 Biomarker phenotype GENOMICS_ENGLAND Emerging therapeutic targets in the short QT syndrome. 29697308 2018
CUI: C0039070
Disease: Syncope
Syncope 		0.410 Biomarker phenotype HPO