Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		1.000 GermlineCausalMutation ORPHANET Permanent neonatal diabetes caused by a novel mutation in the INS gene. 23107109

2013
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		1.000 GermlineCausalMutation ORPHANET [Permanent neonatal diabetes and recessive mutation in the INS gene: a familial history]. 23245869

2013
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		1.000 GermlineCausalMutation ORPHANET The lessons of early-onset monogenic diabetes for the understanding of diabetes pathogenesis. 22498247

2012
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		1.000 GermlineCausalMutation ORPHANET Review on monogenic diabetes. 21844708

2011