Disease: Hypertensive disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.340 AlteredExpression group BEFREE SHIP2 mouse models and genetic studies in human propose that increased expression or activity of SHIP2 contributes to the pathogenesis of the metabolic syndrome, hypertension and type 2 diabetes. 31342643 2020
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.340 GeneticVariation group BEFREE In addition, the G allele of SHIP2 (+2945A/G) seemed to increase the susceptibility to hypertension for T2DM patients. 25635986 2015
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.340 GeneticVariation group BEFREE These results suggest that INPPL1 variants may be involved in mechanisms causing hypertension in metabolic syndrome patients specifically. 17557929 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.340 Biomarker group CTD_human In a cohort of 905 French type 2 diabetic patients, we found evidence of association of INPPL1 SNPs with the presence of hypertension. 15220217 2004
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.340 Biomarker group BEFREE In a cohort of 905 French type 2 diabetic patients, we found evidence of association of INPPL1 SNPs with the presence of hypertension. 15220217 2004