Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10345
Gene Symbol: TRDN
TRDN
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.300 GermlineCausalMutation ORPHANET KCNQ1 mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1. 27041150

2016