SLC6A8, solute carrier family 6 member 8, 6535

N. diseases: 274; N. variants: 27
Disease: Premature ventricular contractions ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		0.020 Biomarker phenotype BEFREE A 53-year-old male with heart failure secondary to anterior wall myocardial infarction treated with cardiac resynchronization-defibrillator (CRT-D) device presented with ventricular arrhythmia: repetitive incessant slow ventricular tachycardias (VT) below the CRT-D detection zone, accelerated ventricular rhythm, and numerous premature ventricular ectopic beats (ExV), resulting in loss of biventricular pacing. 31241241 2019
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		0.020 GeneticVariation phenotype LHGDN Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8. 18443316 2008