KCNQ4

potassium voltage-gated channel subfamily Q member 4
OMIM: 603537
PanelMode of inheritanceDetails
1 panel
R-numbers: R67
Signed-off version 3.3
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
#600101:Deafness, autosomal dominant 2A