Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.320 GermlineCausalMutation ORPHANET Genotype- and phenotype-guided management of congenital long QT syndrome. 24093767

2013