KCNQ4

potassium voltage-gated channel subfamily Q member 4
OMIM: 603537
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.42
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
Deafness, autosomal dominant 2A, OMIM:600101