SLC6A2, solute carrier family 6 member 2, 6530

N. diseases: 238; N. variants: 24
Disease: Mitral Valve Prolapse Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
Mitral Valve Prolapse Syndrome 		0.300 GermlineCausalMutation disease ORPHANET Orthostatic intolerance and tachycardia associated with norepinephrine-transporter deficiency. 10684912 2000