HNF1A, HNF1 homeobox A, 6927

N. diseases: 292; N. variants: 105
Disease: K ATP Permanent Neonatal Diabetes ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes 		0.010 GeneticVariation disease BEFREE Some other forms of monogenic diabetes associated with impaired function of the beta-cell, such as MODY3 and PNDM linked to mutations in Kir6.2 and SUR1 genes, can be successfully managed by sulphonylurea agents. 17488343 2008