CYP11B2

cytochrome P450 family 11 subfamily B member 2
OMIM: 124080
PanelMode of inheritanceDetails
1 panel
R-numbers: R150
Signed-off version 3.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hypoaldosteronism, congenital, due to CMO I deficiency, OMIM:203400, Hypoaldosteronism, congenital, due to CMO II deficiency, OMIM:610600, Aldosterone to renin ratio raised