Genomics England
GMS Panels
Panels
Genes and Entities

WNT10A

Wnt family member 10A
OMIM: 606268
PanelMode of inheritanceDetails
1 panel
Green
in Ectodermal dysplasia
R-numbers: R163
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Schopf-Schulz-Passarge syndrome, OMIM:224750, Odontoonychodermal dysplasia, OMIM:257980