Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.130 GeneticVariation group BEFREE Loss of function mutations of the ecto-nucleotide pyrophosphatase/pyrophosphodiesterase 1 gene (ENPP1) causes a wide spectrum of phenotypes, ranging from lethal generalized arterial calcification of infancy to hypophosphatemic rickets with hypertension. 25741938 2015
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.130 Biomarker group BEFREE The ancestral alleles of these SNPs have previously been associated with nutrition-related diseases hypertension (AGT and CYP3A7) and insulin resistance (ENPP1). 23036011 2012
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.130 GeneticVariation group LHGDN We conclude that the interaction between the K121Q polymorphism of the PC-1 gene and birth length affects insulin sensitivity and increases susceptibility to type 2 diabetes and hypertension in adulthood. 15126519 2004
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.130 GeneticVariation group BEFREE We conclude that the interaction between the K121Q polymorphism of the PC-1 gene and birth length affects insulin sensitivity and increases susceptibility to type 2 diabetes and hypertension in adulthood. 15126519 2004
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.130 Biomarker group HPO