INS, insulin, 3630

N. diseases: 405; N. variants: 37
Disease: Monogenic diabetes ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 GeneticVariation disease BEFREE Mutations in the K-ATP channel and INS genes were the most common cause of early diagnosed monogenic diabetes. 27167055 2016
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 GeneticVariation disease CLINVAR INS-gene mutations: from genetics and beta cell biology to clinical disease. 25542748 2015
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 GeneticVariation disease CLINVAR Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). 20226046 2010
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 GeneticVariation disease CLINVAR Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood. 18162506 2008
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 GeneticVariation disease CLINVAR Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. 18192540 2008
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 GeneticVariation disease CLINVAR Insulin gene mutations as a cause of permanent neonatal diabetes. 17855560 2007
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 Biomarker disease GENOMICS_ENGLAND
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		0.410 Biomarker disease GENOMICS_ENGLAND