WNT10A

Wnt family member 10A
OMIM: 606268
PanelMode of inheritanceDetails
1 panel
R-numbers: R163
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Schopf-Schulz-Passarge syndrome, OMIM:224750, Odontoonychodermal dysplasia, OMIM:257980