TPH2, tryptophan hydroxylase 2, 121278

N. diseases: 137; N. variants: 37
Disease: Muscular Dystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.010 GeneticVariation disease BEFREE Our findings suggest that the A-G polymorphism of TPH2 may confer susceptibility to suicide behavior in MD patients. 17011525 2006