UCP2, uncoupling protein 2, 7351

N. diseases: 235; N. variants: 5
Disease: Hyperinsulinism due to uncoupling protein 2 deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4303082
Disease: Hyperinsulinism due to uncoupling protein 2 deficiency
Hyperinsulinism due to uncoupling protein 2 deficiency 		0.300 GermlineCausalMutation disease ORPHANET Molecular mechanisms of congenital hyperinsulinism. 25733449 2015
CUI: C4303082
Disease: Hyperinsulinism due to uncoupling protein 2 deficiency
Hyperinsulinism due to uncoupling protein 2 deficiency 		0.300 GermlineCausalMutation disease ORPHANET Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion. 19065272 2008