Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6330
Gene Symbol: SCN4B
SCN4B
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.300 GermlineCausalMutation ORPHANET Genotype- and phenotype-guided management of congenital long QT syndrome. 24093767

2013