NR3C2

nuclear receptor subfamily 3 group C member 2
OMIM: 600983
PanelMode of inheritanceDetails
1 panel
R-numbers: R198
Signed-off version 2.23
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Pseudohypoaldosteronism type I, autosomal dominant, 177735, Hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy, 605115 no inheritance pattern