Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.500 GermlineCausalMutation ORPHANET Genotype- and phenotype-guided management of congenital long QT syndrome. 24093767

2013