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: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
0.020 GeneticVariation phenotype BEFREE Outcome may vary between primary and secondary AI mainly due to differences in the renin-angiotensin-aldosterone system (RAAS). 29376070 2017
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
0.020 GeneticVariation phenotype BEFREE MC2R mutations should be considered in children who have primary adrenal failure with apparent mild disturbances in renin-sodium homeostasis. 17223989 2007