WNT10A

Wnt family member 10A
OMIM: 606268
PanelMode of inheritanceDetails
1 panel
R-numbers: R163
Signed-off version 1.10
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Schopf-Schulz-Passarge syndrome 224750, Odontoonychodermal dysplasia 257980