KRT17

PanelMode of inheritanceDetails
1 panel
R-numbers: R165
Signed-off version 2.1
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
Steatocystoma multiplex, OMIM:184500, Pachyonychia congenita 2, OMIM:167210