ACOT13, acyl-CoA thioesterase 13, 55856

N. diseases: 17; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272002
Disease: alpha^0^ Thalassemia
alpha^0^ Thalassemia
0.010 GeneticVariation disease BEFREE Two of them (2/69, 3.0%) were found to be double heterozygotes for β(0)-thalassemia and α(0)-thalassemia. 24356175 2014