SASH1

SAM and SH3 domain containing 1
OMIM: 607955
PanelMode of inheritanceDetails
1 panel
R-numbers: R236
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Pigmentation defects, palmoplantar keratoderma, spinocellular carcinoma (homo), DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1, DUH1, Dyschromatosis (het)