CTNNA3, catenin alpha 3, 29119

N. diseases: 73; N. variants: 33
Disease: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1832931
Disease: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 		0.300 GermlineCausalMutation disease ORPHANET Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy. 23136403 2013