REN, renin, 5972

N. diseases: 721; N. variants: 25
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.050 AlteredExpression disease BEFREE This review summarizes our current knowledge on the genetic determinants that contribute to variations in plasma aldosterone and renin levels in the general population and the genetics of familial and sporadic PA. 23610123 2013
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.050 Biomarker disease BEFREE Although evidence shows a close link between arrhythmia and the renin-angiotensin system (RAS), it remains to be determined whether the RAS is involved in the pathogenesis of non-familial SSS. 22242192 2012
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.050 GeneticVariation disease BEFREE Some causes of low renin hypertension are familial with known genetic bases. 15808808 2005
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.050 GeneticVariation disease BEFREE The diagnosis was suspected as a likely cause of familial low renin hypertension and was confirmed by findings of reduced basal and ACTH-stimulated serum and urinary levels of cortisol and other 17-hydroxysteroids, together with hypergonadotropic hypogonadism in both 46,XY and 46,XX patients, and abnormally increased secretion of 17-desoxysteroids, such as progesterone, 11-deoxycorticosterone, and corticosterone. 2493025 1989
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.050 GeneticVariation disease BEFREE Calf muscle haemodynamics and the renin-angiotensin-aldosterone system in normotensive subjects with a familial predisposition to hypertension: changes during increased salt intake. 6397530 1984