Disease: Short QT Syndrome 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1865020
Disease: Short QT Syndrome 1
Short QT Syndrome 1 		0.300 GermlineCausalMutation disease ORPHANET Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6). 21383000 2011