SNTA1, syntrophin alpha 1, 6640

N. diseases: 45; N. variants: 6
Disease: Romano-Ward Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		0.300 GermlineCausalMutation disease ORPHANET Genotype- and phenotype-guided management of congenital long QT syndrome. 24093767 2013