IGF2, insulin like growth factor 2, 3481

N. diseases: 604; N. variants: 19
Disease: Congenital hemihypertrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy 		0.400 GermlineCausalMutation disease ORPHANET IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia. 18159214 2008
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy 		0.400 Biomarker disease HPO