SCNN1G

sodium channel epithelial 1 gamma subunit
OMIM: 600761
PanelMode of inheritanceDetails
2 panels
R-numbers: R198
Signed-off version 2.23
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Pseudohypoaldosteronism, type I, 264350
R-numbers: R189
Signed-off version 1.3
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Liddle syndrome, 177200, Ciliopathies, Bronchiectasis, Bronchiectasis with or without elevated sweat chloride 3, 613071, Pseudohypoaldosteronism, type I, 264350