DIS3L2, DIS3 like 3'-5' exoribonuclease 2, 129563

N. diseases: 91; N. variants: 22
Disease: Congenital hypertrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0332887
Disease: Congenital hypertrophy
Congenital hypertrophy 		0.010 GeneticVariation disease BEFREE Loss of function of the DIS3L2 exoribonuclease is associated with Wilms tumor and the Perlman congenital overgrowth syndrome. 29950491 2018