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 		0.010 GeneticVariation disease BEFREE Mosaic paternal uniparental isodisomy and an ABCC8 gene mutation in a patient with permanent neonatal diabetes and hemihypertrophy. 17942821 2008